Variant report

Variant	esv3410118
Chromosome Location	chr10:42399439-42817641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5851)
CpG islands
(count:2078)
Chromatin interactive
region (count:71)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5851 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:42799540-42800192	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:42597838-42598531	K562	blood:	n/a	n/a
3	ARID3A	chr10:42597406-42597416	K562	blood:	n/a	n/a
4	ARID3A	chr10:42535480-42535514	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:42599390-42600242	K562	blood:	n/a	n/a
6	ARID3A	chr10:42401028-42401058	HepG2	liver:	n/a	n/a
7	ATF1	chr10:42801380-42801410	K562	blood:	n/a	n/a
8	ATF1	chr10:42405122-42405316	K562	blood:	n/a	n/a
9	ATF1	chr10:42427144-42427345	K562	blood:	n/a	n/a
10	ATF1	chr10:42534553-42534934	K562	blood:	n/a	n/a
11	ATF1	chr10:42799538-42800192	K562	blood:	n/a	n/a
12	ATF1	chr10:42599330-42600242	K562	blood:	n/a	n/a
13	ATF1	chr10:42597833-42598535	K562	blood:	n/a	n/a
14	ATF1	chr10:42539003-42539017	K562	blood:	n/a	n/a
15	ATF1	chr10:42535479-42535678	K562	blood:	n/a	n/a
16	ATF1	chr10:42797113-42797490	K562	blood:	n/a	n/a
17	ATF1	chr10:42815222-42815574	K562	blood:	n/a	n/a
18	ATF1	chr10:42529120-42532936	K562	blood:	n/a	n/a
19	ATF1	chr10:42817203-42817917	K562	blood:	n/a	n/a
20	ATF1	chr10:42539718-42539917	K562	blood:	n/a	n/a
21	ATF3	chr10:42529049-42531144	GM12878	blood:	n/a	n/a
22	BACH1	chr10:42418459-42418832	K562	blood:	n/a	n/a
23	BACH1	chr10:42597763-42598620	K562	blood:	n/a	n/a
24	BACH1	chr10:42407053-42407775	K562	blood:	n/a	n/a
25	BACH1	chr10:42813274-42813746	K562	blood:	n/a	n/a
26	BACH1	chr10:42599263-42600248	K562	blood:	n/a	n/a
27	BATF	chr10:42648114-42648316	GM12878	blood:	n/a	n/a
28	BATF	chr10:42704442-42704772	GM12878	blood:	n/a	chr10:42704640-42704651
29	BATF	chr10:42531702-42546600	GM12878	blood:	n/a	n/a
30	BATF	chr10:42614296-42614594	GM12878	blood:	n/a	n/a
31	BATF	chr10:42596622-42600748	GM12878	blood:	n/a	n/a
32	BATF	chr10:42648105-42648599	GM12878	blood:	n/a	n/a
33	BATF	chr10:42673852-42674316	GM12878	blood:	n/a	n/a
34	BATF	chr10:42678782-42679680	GM12878	blood:	n/a	n/a
35	BATF	chr10:42428654-42428879	GM12878	blood:	n/a	n/a
36	BATF	chr10:42610090-42610374	GM12878	blood:	n/a	n/a
37	BATF	chr10:42676194-42676528	GM12878	blood:	n/a	n/a
38	BATF	chr10:42663387-42664486	GM12878	blood:	n/a	n/a
39	BATF	chr10:42696631-42696866	GM12878	blood:	n/a	n/a
40	BATF	chr10:42648356-42648599	GM12878	blood:	n/a	n/a
41	BATF	chr10:42791080-42791784	GM12878	blood:	n/a	n/a
42	BATF	chr10:42684572-42684848	GM12878	blood:	n/a	n/a
43	BATF	chr10:42401651-42402639	GM12878	blood:	n/a	n/a
44	BATF	chr10:42406088-42407143	GM12878	blood:	n/a	n/a
45	BATF	chr10:42409538-42409868	GM12878	blood:	n/a	n/a
46	BATF	chr10:42611063-42611437	GM12878	blood:	n/a	n/a
47	BATF	chr10:42408156-42408502	GM12878	blood:	n/a	n/a
48	BATF	chr10:42666434-42667002	GM12878	blood:	n/a	n/a
49	BATF	chr10:42611144-42611526	GM12878	blood:	n/a	n/a
50	BATF	chr10:42765314-42765560	GM12878	blood:	n/a	n/a

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42529592-42529642	SK-N-SH	brain:	n/a
2	chr10:42677108-42677158	SK-N-SH	brain:	n/a
3	chr10:42777375-42777425	HCT-116	colon:	n/a
4	chr10:42777525-42777575	MCF10A-Er-Src	breast:	n/a
5	chr10:42529592-42529642	SK-N-SH	brain:	n/a
6	chr10:42677108-42677158	SK-N-SH	brain:	n/a
7	chr10:42777375-42777425	HCT-116	colon:	n/a
8	chr10:42777525-42777575	MCF10A-Er-Src	breast:	n/a
9	chr10:42677108-42677158	AG09319	gingival:	n/a
10	chr10:42745966-42746016	GM19239	blood:	n/a
11	chr10:42607194-42607244	SK-N-SH	brain:	n/a
12	chr10:42738239-42738289	HCT-116	colon:	n/a
13	chr10:42401915-42401965	HCPEpiC	choroid plexus:	n/a
14	chr10:42777403-42777453	HCM	heart:	n/a
15	chr10:42777375-42777425	ovcar-3	ovarian:	n/a
16	chr10:42673902-42673952	GM12878	blood:	n/a
17	chr10:42401915-42401965	HIPEpiC	eye:	n/a
18	chr10:42401915-42401965	AG10803	skin:	n/a
19	chr10:42672859-42672909	NHDF-neo	bronchial:	n/a
20	chr10:42737322-42737372	Caco-2	colon:	n/a
21	chr10:42608749-42608799	Jurkat	blood:	n/a
22	chr10:42529747-42529797	AoSMC	blood vessel:	n/a
23	chr10:42672859-42672909	HCPEpiC	choroid plexus:	n/a
24	chr10:42607194-42607244	AG09309	skin:	n/a
25	chr10:42529592-42529642	NT2-D1	testis:	n/a
26	chr10:42607194-42607244	ovcar-3	ovarian:	n/a
27	chr10:42641430-42641480	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:42530427-42530477	NT2-D1	testis:	n/a
29	chr10:42608749-42608799	H1-hESC	embryonic stem cell:	embryo
30	chr10:42406286-42406336	AG10803	skin:	n/a
31	chr10:42673902-42673952	ECC-1	luminal epithelium:	n/a
32	chr10:42645466-42645516	AG04449	skin:	fetal
33	chr10:42401915-42401965	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:42530427-42530477	HAEpiC	amniotic membrane:	n/a
35	chr10:42644887-42644937	AoSMC	blood vessel:	n/a
36	chr10:42641430-42641480	HL-60	blood:	n/a
37	chr10:42644887-42644937	HMEC	breast:	n/a
38	chr10:42606808-42606858	MCF-7	breast:	n/a
39	chr10:42737139-42737189	SK-N-MC	brain:	n/a
40	chr10:42646111-42646161	ProgFib	skin:	n/a
41	chr10:42641430-42641480	ovcar-3	ovarian:	n/a
42	chr10:42777403-42777453	MCF-7	breast:	n/a
43	chr10:42737582-42737632	HCM	heart:	n/a
44	chr10:42644887-42644937	GM12878	blood:	n/a
45	chr10:42529592-42529642	SAEC	small airway:	n/a
46	chr10:42642959-42643009	HCF	heart:	n/a
47	chr10:42738538-42738588	AG09319	gingival:	n/a
48	chr10:42642959-42643009	U87	brain:	n/a
49	chr10:42737322-42737372	MCF-7	breast:	n/a
50	chr10:42745966-42746016	U87	brain:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:121484020..121484634-chr10:42530561..42531081,2	MCF-7	breast:
2	chr10:42528107..42529933-chr8:110778066..110779566,2	MCF-7	breast:
3	chr10:42532093..42532747-chr2:154892410..154892910,2	MCF-7	breast:
4	chr10:42529603..42530301-chr17:58166691..58167257,2	MCF-7	breast:
5	chr1:149222942..149224601-chr10:42397745..42399854,2	MCF-7	breast:
6	chr10:42398850..42399800-chr10:42529302..42530219,2	MCF-7	breast:
7	chr1:121482971..121485434-chr10:42543133..42544641,3	MCF-7	breast:
8	chr10:42529082..42529941-chr19:27738664..27739193,3	MCF-7	breast:
9	chr10:42528736..42531443-chr2:73087371..73089045,2	MCF-7	breast:
10	chr10:42526394..42527915-chr7:61967791..61969362,3	MCF-7	breast:
11	chr10:42528102..42529921-chr12:34831375..34832895,2	K562	blood:
12	chr10:42527395..42527915-chr7:61970565..61971091,3	MCF-7	breast:
13	chr10:42525601..42527915-chr7:61967079..61969278,2	K562	blood:
14	chr10:42529302..42529920-chr19:27734982..27735519,2	MCF-7	breast:
15	chr10:42673929..42674445-chr10:43600657..43601190,2	K562	blood:
16	chr10:42532112..42532613-chr19:27734969..27735848,2	MCF-7	breast:
17	chr10:10531872..10532392-chr10:42529084..42529944,2	MCF-7	breast:
18	chr10:42529442..42530392-chr19:27737662..27738480,2	MCF-7	breast:
19	chr1:121484509..121485410-chr10:42528540..42529041,2	MCF-7	breast:
20	chr10:42398870..42399833-chr14:43322802..43323708,2	MCF-7	breast:
21	chr1:121484711..121485401-chr10:42532112..42532774,3	MCF-7	breast:
22	chr10:42531904..42532590-chr13:98148609..98149589,2	MCF-7	breast:
23	chr10:42531427..42532425-chr11:19922614..19923134,2	MCF-7	breast:
24	chr1:121484248..121485086-chr10:42528519..42529041,2	MCF-7	breast:
25	chr10:42398850..42399487-chr10:42529302..42530228,2	MCF-7	breast:
26	chr10:42397869..42400416-chr19:27731046..27733513,2	MCF-7	breast:
27	chr1:121482838..121485428-chr10:42528872..42531081,8	K562	blood:
28	chr10:42530906..42532591-chr12:125398363..125400597,2	MCF-7	breast:
29	chr10:42526475..42528192-chr19:27731227..27733212,2	MCF-7	breast:
30	chr10:42528281..42529803-chr7:129794745..129796264,2	MCF-7	breast:
31	chr10:42527415..42527915-chr7:61968777..61969450,2	MCF-7	breast:
32	chr1:224620434..224622448-chr10:42530903..42532481,2	MCF-7	breast:
33	chr10:42529415..42529944-chr19:27739260..27739782,2	MCF-7	breast:
34	chr1:121483719..121484637-chr10:42529281..42529801,2	MCF-7	breast:
35	chr1:121483933..121485433-chr10:42530465..42531081,9	MCF-7	breast:
36	chr10:42530145..42531061-chr19:27738673..27739367,3	MCF-7	breast:
37	chr10:42399009..42399706-chr10:42529715..42530239,2	MCF-7	breast:
38	chr10:42529561..42531107-chr15:41406107..41408391,2	MCF-7	breast:
39	chr10:42528075..42531081-chr19:27735905..27739791,6	MCF-7	breast:
40	chr10:42527395..42527923-chr7:61968860..61969524,4	MCF-7	breast:
41	chr1:121484906..121485408-chr10:42529869..42530392,2	MCF-7	breast:
42	chr10:42527395..42527914-chr7:61968778..61969295,2	MCF-7	breast:
43	chr1:121482909..121485419-chr10:42527541..42532488,18	MCF-7	breast:
44	chr10:42739123..42739644-chr10:101379768..101380454,2	HCT-116	colon:
45	chr10:42398850..42399487-chr10:42529302..42530228,2	MCF-7	breast:
46	chr10:42530231..42530737-chr16:29006682..29007182,2	MCF-7	breast:
47	chr10:42530427..42532590-chr8:46977725..46979226,2	MCF-7	breast:
48	chr10:42673795..42674377-chr10:42765091..42765784,2	MCF-7	breast:
49	chr10:42673795..42674377-chr10:42765091..42765784,2	MCF-7	breast:
50	chr10:42528302..42530981-chr19:27731210..27733512,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNYL2-5	chr10:42796822-42796961	NONHSAT012863
2	lnc-BMS1-12	chr10:42400201-42400696	NONHSAT012847
3	lnc-BMS1-10	chr10:42529283-42529832	FPKM1_group_3228_transcript_1
4	lnc-CCNYL2-9	chr10:42596697-42596905	NONHSAT012853
5	lnc-BMS1-10	chr10:42529998-42530003	FPKM1_group_3228_transcript_1
6	lnc-CCNYL2-6	chr10:42775182-42777267	NONHSAT012861
7	lnc-BMS1-12	chr10:42423481-42423551	NONHSAT012847
8	lnc-BMS1-12	chr10:42406916-42406946	NONHSAT012847
9	lnc-BMS1-9	chr10:42687963-42689514	NONHSAT012855
10	lnc-CCNYL2-5	chr10:42794471-42794553	NONHSAT012863
11	lnc-BMS1-8	chr10:42705438-42705831	NONHSAT012856
12	lnc-BMS1-12	chr10:42399434-42399525	NONHSAT012847
13	lnc-BMS1-6	chr10:42791078-42791322	NONHSAT012862
14	lnc-CCNYL2-9	chr10:42598751-42598801	NONHSAT012853
15	lnc-BMS1-10	chr10:42529283-42529832	NONHSAT012852
16	lnc-CCNYL2-5	chr10:42795737-42796013	NONHSAT012863
17	lnc-CCNYL2-10	chr10:42501405-42501470	NONHSAT012851
18	lnc-BMS1-10	chr10:42529998-42530057	NONHSAT012852
19	lnc-CCNYL2-10	chr10:42489651-42489811	NONHSAT012851
20	lnc-CCNYL2-11	chr10:42406659-42406684	NONHSAT012850
21	lnc-BMS1-7	chr10:42737930-42738014	NONHSAT012859
22	lnc-CCNYL2-10	chr10:42498812-42498914	NONHSAT012851
23	lnc-CCNYL2-10	chr10:42506989-42507177	NONHSAT012851
24	lnc-BMS1-9	chr10:42686975-42687136	NONHSAT012855
25	lnc-CCNYL2-11	chr10:42407539-42407748	NONHSAT012850
26	lnc-BMS1-7	chr10:42746444-42746645	NONHSAT012859

No data

Variant related genes	Relation type
ENSG00000264398	TF binding region
KSR1P1	TF binding region
PABPC1P8	TF binding region
ENSG00000271650	TF binding region
IGKV1OR10-1	TF binding region
ENSG00000264398	CpG island
KSR1P1	CpG island
PABPC1P8	CpG island
ENSG00000271650	CpG island
IGKV1OR10-1	CpG island
ENSG00000128908	chromatin interactions
ENSG00000155287	chromatin interactions
ENSG00000265345	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000162923	chromatin interactions
ENSG00000143786	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 28451 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:28451 , 50 per page) page: 1 2 3 4 5 6 7 ... 570

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199860889	chr10:42399447-42399448	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs369505632	chr10:42399448-42399449	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs372722357	chr10:42399451-42399452	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs74216426	chr10:42399455-42399456	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs368202105	chr10:42399456-42399457	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs375705326	chr10:42399461-42399462	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs71502121	chr10:42399462-42399463	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs74209528	chr10:42399466-42399467	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs71229590	chr10:42399469-42399470	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs372497484	chr10:42399470-42399471	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs553673983	chr10:42399480-42399481	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs377554062	chr10:42399482-42399483	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs371030958	chr10:42399487-42399488	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs375260107	chr10:42399489-42399490	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs200679166	chr10:42399497-42399498	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs573459385	chr10:42399498-42399499	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs370677988	chr10:42399501-42399502	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs375043689	chr10:42399503-42399504	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs369881771	chr10:42399508-42399509	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs367974316	chr10:42399510-42399511	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs542465818	chr10:42399514-42399515	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs371797623	chr10:42399518-42399519	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs376501654	chr10:42399519-42399520	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs562080939	chr10:42399525-42399526	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs61847636	chr10:42399526-42399527	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200803421	chr10:42399529-42399530	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs202086131	chr10:42399530-42399531	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372205685	chr10:42399538-42399539	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74187360	chr10:42399540-42399541	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs71237475	chr10:42399548-42399549	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376517371	chr10:42399550-42399551	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369456425	chr10:42399552-42399553	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575681643	chr10:42399559-42399560	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs78541446	chr10:42399560-42399561	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372357265	chr10:42399563-42399564	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs71257283	chr10:42399564-42399565	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71241792	chr10:42399567-42399568	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373126791	chr10:42399569-42399570	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78563892	chr10:42399573-42399574	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs80251060	chr10:42399574-42399575	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375033514	chr10:42399575-42399576	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369183039	chr10:42399580-42399581	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372599790	chr10:42399581-42399582	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376078827	chr10:42399582-42399583	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371549774	chr10:42399583-42399584	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373310834	chr10:42399592-42399593	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375542223	chr10:42399594-42399595	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377337928	chr10:42399595-42399596	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371098134	chr10:42399598-42399599	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs77469397	chr10:42399600-42399601	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20858243	CNVD
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2437 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42373600-42399600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:42373600-42399600	ZNF genes & repeats	Fetal Kidney	kidney
3	chr10:42373600-42400800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr10:42373600-42400800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:42373600-42400800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:42373600-42400800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:42373600-42400800	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:42373600-42400800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
9	chr10:42373600-42400800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
10	chr10:42373600-42400800	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
11	chr10:42373600-42400800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
12	chr10:42373600-42400800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
13	chr10:42373600-42400800	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr10:42373600-42400800	ZNF genes & repeats	Brain Angular Gyrus	brain
15	chr10:42373600-42400800	ZNF genes & repeats	Brain Anterior Caudate	brain
16	chr10:42373600-42400800	ZNF genes & repeats	Brain Hippocampus Middle	brain
17	chr10:42373600-42400800	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
18	chr10:42373600-42400800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
19	chr10:42373600-42400800	ZNF genes & repeats	Brain Substantia Nigra	brain
20	chr10:42373600-42400800	ZNF genes & repeats	Colon Smooth Muscle	Colon
21	chr10:42373600-42400800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
22	chr10:42373600-42400800	ZNF genes & repeats	Fetal Heart	heart
23	chr10:42373600-42400800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
24	chr10:42373600-42400800	ZNF genes & repeats	Fetal Lung	lung
25	chr10:42373600-42400800	ZNF genes & repeats	Gastric	stomach
26	chr10:42373600-42400800	ZNF genes & repeats	Left Ventricle	heart
27	chr10:42373600-42400800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
28	chr10:42373600-42400800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
29	chr10:42373600-42400800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
30	chr10:42373600-42400800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
31	chr10:42373600-42400800	ZNF genes & repeats	Dnd41	blood
32	chr10:42373600-42400800	ZNF genes & repeats	HMEC	breast
33	chr10:42373600-42400800	ZNF genes & repeats	HSMMtube	muscle
34	chr10:42373600-42400800	ZNF genes & repeats	NH-A	brain
35	chr10:42373600-42401200	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
36	chr10:42373600-42402200	ZNF genes & repeats	Colonic Mucosa	Colon
37	chr10:42373600-42402400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
38	chr10:42373600-42402400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
39	chr10:42373600-42402400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr10:42373600-42402400	ZNF genes & repeats	Fetal Stomach	stomach
41	chr10:42373600-42402600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
42	chr10:42373600-42402600	ZNF genes & repeats	Liver	Liver
43	chr10:42373600-42402600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
44	chr10:42373600-42402600	ZNF genes & repeats	Fetal Brain Male	brain
45	chr10:42373600-42402800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:42373600-42402800	ZNF genes & repeats	HepG2	liver
47	chr10:42373600-42403600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr10:42373600-42405200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
49	chr10:42373600-42409400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr10:42373600-42409400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood

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