Variant report

Variant	esv1810582
Chromosome Location	chr6:26889428-26990246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1884)
CpG islands
(count:1162)
Chromatin interactive
region (count:35)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1884 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26925619-26925955	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:26924747-26924778	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:26987966-26988366	K562	blood:	n/a	n/a
4	ATF1	chr6:26923925-26924305	K562	blood:	n/a	n/a
5	ATF1	chr6:26987625-26988307	K562	blood:	n/a	n/a
6	ATF2	chr6:26923841-26924229	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:26987181-26988493	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:26923942-26924231	GM12878	blood:	n/a	n/a
9	ATF2	chr6:26987749-26988147	GM12878	blood:	n/a	n/a
10	ATF2	chr6:26987616-26988436	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:26923847-26924306	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:26987495-26988480	GM12878	blood:	n/a	n/a
13	ATF3	chr6:26987802-26988596	K562	blood:	n/a	chr6:26988025-26988034 chr6:26988027-26988036
14	ATF3	chr6:26987803-26988502	A549	lung:	n/a	chr6:26988025-26988034 chr6:26988027-26988036
15	ATF3	chr6:26987804-26988568	A549	lung:	n/a	chr6:26988025-26988034 chr6:26988027-26988036
16	BACH1	chr6:26924664-26924943	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:26987513-26988245	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:26919077-26919488	GM12878	blood:	n/a	n/a
19	BATF	chr6:26925319-26925723	GM12878	blood:	n/a	n/a
20	BATF	chr6:26923172-26923556	GM12878	blood:	n/a	n/a
21	BATF	chr6:26896440-26896670	GM12878	blood:	n/a	chr6:26896493-26896502
22	BATF	chr6:26917548-26917891	GM12878	blood:	n/a	n/a
23	BATF	chr6:26917064-26917394	GM12878	blood:	n/a	n/a
24	BATF	chr6:26896004-26896253	GM12878	blood:	n/a	n/a
25	BATF	chr6:26924423-26924966	GM12878	blood:	n/a	n/a
26	BATF	chr6:26919159-26919394	GM12878	blood:	n/a	n/a
27	BATF	chr6:26929003-26929176	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
28	BATF	chr6:26921657-26921936	GM12878	blood:	n/a	n/a
29	BATF	chr6:26987947-26988327	GM12878	blood:	n/a	n/a
30	BATF	chr6:26911148-26911328	GM12878	blood:	n/a	n/a
31	BATF	chr6:26923787-26924103	GM12878	blood:	n/a	n/a
32	BATF	chr6:26949170-26949399	GM12878	blood:	n/a	chr6:26949247-26949258
33	BATF	chr6:26918546-26918790	GM12878	blood:	n/a	n/a
34	BATF	chr6:26925030-26925340	GM12878	blood:	n/a	n/a
35	BATF	chr6:26923128-26923365	GM12878	blood:	n/a	n/a
36	BATF	chr6:26923753-26924403	GM12878	blood:	n/a	n/a
37	BATF	chr6:26889952-26890170	GM12878	blood:	n/a	n/a
38	BATF	chr6:26928990-26929230	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
39	BATF	chr6:26922534-26922741	GM12878	blood:	n/a	n/a
40	BATF	chr6:26911356-26911600	GM12878	blood:	n/a	n/a
41	BATF	chr6:26920524-26920940	GM12878	blood:	n/a	n/a
42	BATF	chr6:26940264-26940496	GM12878	blood:	n/a	chr6:26940350-26940360
43	BATF	chr6:26968008-26968234	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:26928959-26929218	GM12878	blood:	n/a	chr6:26929119-26929128 chr6:26929120-26929129
45	BCL11A	chr6:26920970-26921280	GM12878	blood:	n/a	n/a
46	BCL11A	chr6:26917021-26917371	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:26923081-26923566	GM12878	blood:	n/a	n/a
48	BCL11A	chr6:26918589-26918831	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:26925060-26925245	GM12878	blood:	n/a	n/a
50	BCL11A	chr6:26921673-26921928	GM12878	blood:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26970375-26970425	HAEpiC	amniotic membrane:	n/a
2	chr6:26987575-26987625	HIPEpiC	eye:	n/a
3	chr6:26983916-26983966	AoSMC	blood vessel:	n/a
4	chr6:26970375-26970425	HAEpiC	amniotic membrane:	n/a
5	chr6:26987575-26987625	HIPEpiC	eye:	n/a
6	chr6:26983916-26983966	AoSMC	blood vessel:	n/a
7	chr6:26914441-26914491	HepG2	liver:	n/a
8	chr6:26988201-26988251	HCM	heart:	n/a
9	chr6:26924550-26924600	SK-N-SH_RA	brain:	n/a
10	chr6:26970382-26970432	NHBE	bronchial:	n/a
11	chr6:26988187-26988237	AG09309	skin:	n/a
12	chr6:26970375-26970425	BE2_C	brain:	n/a
13	chr6:26988177-26988227	AG04449	skin:	fetal
14	chr6:26987810-26987860	PrEC	prostate:	n/a
15	chr6:26987649-26987699	MCF10A-Er-Src	breast:	n/a
16	chr6:26923983-26924033	CMK	blood:	n/a
17	chr6:26970418-26970468	GM06990	blood:	n/a
18	chr6:26988150-26988200	HMEC	breast:	n/a
19	chr6:26914441-26914491	ECC-1	luminal epithelium:	n/a
20	chr6:26987575-26987625	A549	lung:	n/a
21	chr6:26923983-26924033	HepG2	liver:	n/a
22	chr6:26988150-26988200	NT2-D1	testis:	n/a
23	chr6:26988150-26988200	HUVEC	blood vessel:	n/a
24	chr6:26970375-26970425	HEK293	kidney:	embryo
25	chr6:26988150-26988200	PANC-1	pancreas:	n/a
26	chr6:26987575-26987625	GM12891	blood:	n/a
27	chr6:26987966-26988016	AG10803	skin:	n/a
28	chr6:26914441-26914491	LNCaP	prostate:	n/a
29	chr6:26923983-26924033	HIPEpiC	eye:	n/a
30	chr6:26988148-26988198	HMEC	breast:	n/a
31	chr6:26923983-26924033	GM12878	blood:	n/a
32	chr6:26987575-26987625	SAEC	small airway:	n/a
33	chr6:26988201-26988251	K562	blood:	n/a
34	chr6:26924550-26924600	IMR90	lung:	fetal
35	chr6:26988177-26988227	BJ	skin:	n/a
36	chr6:26970382-26970432	HAEpiC	amniotic membrane:	n/a
37	chr6:26923983-26924033	ECC-1	luminal epithelium:	n/a
38	chr6:26987810-26987860	HRCEpiC	kidney:	n/a
39	chr6:26923983-26924033	HCPEpiC	choroid plexus:	n/a
40	chr6:26970382-26970432	IMR90	lung:	fetal
41	chr6:26988201-26988251	HEEpiC	esophagus:	n/a
42	chr6:26988201-26988251	HRE	kidney:	n/a
43	chr6:26987649-26987699	AG09319	gingival:	n/a
44	chr6:26987810-26987860	HUVEC	blood vessel:	n/a
45	chr6:26988201-26988251	HCT-116	colon:	n/a
46	chr6:26970382-26970432	GM12891	blood:	n/a
47	chr6:26988177-26988227	GM12891	blood:	n/a
48	chr6:26987810-26987860	RPTEC	kidney:	n/a
49	chr6:26970382-26970432	SK-N-SH	brain:	n/a
50	chr6:26924550-26924600	RPTEC	kidney:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26922078..26923970-chr6:27032946..27034480,2	K562	blood:
2	chr6:26986672..26989789-chr6:27000178..27003902,5	K562	blood:
3	chr6:26922448..26924229-chr6:27062597..27064654,2	K562	blood:
4	chr6:26985479..26987950-chr6:27115470..27119189,3	K562	blood:
5	chr6:26989531..26991995-chr6:27101331..27103055,2	K562	blood:
6	chr6:26987953..26990006-chr6:27113419..27115152,2	MCF-7	breast:
7	chr6:26981020..26983396-chr6:26986537..26988507,2	K562	blood:
8	chr6:26986141..26989315-chr6:27099693..27102722,3	K562	blood:
9	chr6:26982967..26984525-chr6:26986393..26988764,2	MCF-7	breast:
10	chr6:26962343..26965289-chr6:26986491..26988275,2	MCF-7	breast:
11	chr6:26596362..26598030-chr6:26986586..26989465,2	MCF-7	breast:
12	chr6:26987242..26987893-chr7:27224402..27225817,3	Hela-S3	cervix:
13	chr6:26986421..26989195-chr6:26989696..26993704,4	MCF-7	breast:
14	chr6:26923074..26925467-chr6:26986570..26988926,2	K562	blood:
15	chr6:26156738..26158730-chr6:26923909..26926382,2	K562	blood:
16	chr6:26923074..26925467-chr6:26986570..26988926,2	K562	blood:
17	chr19:14628712..14629433-chr6:26987153..26987946,2	Hela-S3	cervix:
18	chr6:26987473..26989344-chr6:26998770..27002540,3	MCF-7	breast:
19	chr17:57784521..57785212-chr6:26987452..26988274,2	Hela-S3	cervix:
20	chr6:26987456..26989789-chr6:27000178..27002693,2	K562	blood:
21	chr6:26982819..26984564-chr6:27097358..27099150,2	MCF-7	breast:
22	chr6:26923847..26925381-chr6:26927830..26930168,2	MCF-7	breast:
23	chr6:26990084..26991852-chr6:26998838..27000501,2	K562	blood:
24	chr14:69262422..69263047-chr6:26987347..26987885,2	Hela-S3	cervix:
25	chr6:26972821..26975346-chr6:26986286..26989027,2	MCF-7	breast:
26	chr6:26986048..26988342-chr8:145752952..145755516,2	MCF-7	breast:
27	chr17:41465565..41466625-chr6:26987146..26987924,3	Hela-S3	cervix:
28	chr6:26595477..26598975-chr6:26986599..26989051,3	K562	blood:
29	chr6:26981020..26983356-chr6:26987007..26989080,2	K562	blood:
30	chr6:26985450..26988105-chr6:27045850..27047500,2	MCF-7	breast:
31	chr6:26984517..26987558-chr6:27114844..27118059,3	K562	blood:
32	chr1:113498267..113498942-chr6:26987110..26987703,2	Hela-S3	cervix:
33	chr17:41438167..41438688-chr6:26987450..26987968,2	Hela-S3	cervix:
34	chr6:26969414..26971961-chr6:26985558..26987515,2	K562	blood:
35	chr6:26987415..26988064-chr6:28891401..28892216,2	Hela-S3	cervix:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AG-2	chr6:26988415-26988434	ENSG00000224843
2	lnc-HIST1H2AG-3	chr6:26936241-26936301	NONHSAT108319
3	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108319
4	lnc-HIST1H2AG-3	chr6:26924772-26924962	ENSG00000224843.2
5	lnc-HIST1H2BJ-8	chr6:26987145-26988085	NONHSAT108323
6	lnc-HIST1H2AG-3	chr6:26936797-26936850	XLOC_005216
7	lnc-HIST1H2BJ-10	chr6:26892898-26893054	NONHSAT108318
8	lnc-HIST1H2BJ-9	chr6:26968987-26969427	ENSG00000272312.1
9	lnc-HIST1H2AG-3	chr6:26988232-26991804	NONHSAT108325
10	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2
11	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2
12	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108320
13	lnc-HIST1H2AG-3	chr6:26926892-26926895	NONHSAT108319
14	lnc-HIST1H2AG-2	chr6:26988232-26988434	ENSG00000224843
15	lnc-HIST1H2BJ-10	chr6:26924168-26924285	NONHSAT108318
16	lnc-HIST1H2AG-3	chr6:26924879-26924962	XLOC_005216
17	lnc-HIST1H2BJ-8	chr6:26985858-26989416	NONHSAT108322
18	lnc-HIST1H2AG-3	chr6:26936797-26942146	ENSG00000224843.2
19	lnc-HIST1H2AG-3	chr6:26924771-26924962	ENSG00000224843.2
20	lnc-HIST1H2AG-3	chr6:26936237-26936301	NONHSAT108320
21	lnc-HIST1H2AG-3	chr6:26936237-26936301	XLOC_005216

No data

Variant related genes	Relation type
GUSBP2	TF binding region
LINC00240	TF binding region
ENSG00000272312	TF binding region
TRNAI2	TF binding region
GUSBP2	CpG island
LINC00240	CpG island
ENSG00000272312	CpG island
TRNAI2	CpG island
ENSG00000213563	chromatin interactions
ENSG00000238621	chromatin interactions
ENSG00000005073	chromatin interactions
ENSG00000141378	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000132002	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000240990	chromatin interactions
ENSG00000272312	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000241549	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000146109	chromatin interactions
ENSG00000220581	chromatin interactions
ENSG00000224843	chromatin interactions
ENSG00000204713	chromatin interactions
ENSG00000196787	chromatin interactions

Extended variants
information (count: 1685 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573210425	chr6:26889467-26889468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545185589	chr6:26889549-26889550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565184751	chr6:26889598-26889599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140967207	chr6:26889639-26889640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6928511	chr6:26889645-26889646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs182381274	chr6:26889725-26889726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545057387	chr6:26889727-26889728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146994277	chr6:26889734-26889735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6933132	chr6:26889752-26889753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs6910684	chr6:26889762-26889763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534964909	chr6:26889794-26889795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186467282	chr6:26889813-26889814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190909081	chr6:26889863-26889864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182526111	chr6:26889945-26889946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556987761	chr6:26889950-26889951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567250333	chr6:26889964-26889965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187967414	chr6:26890012-26890013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552591027	chr6:26890077-26890078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573196458	chr6:26890079-26890080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145597170	chr6:26890109-26890110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17278688	chr6:26890136-26890137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs193090351	chr6:26890173-26890174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9766136	chr6:26890193-26890194	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs9767110	chr6:26890194-26890195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs530178346	chr6:26890305-26890306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565418819	chr6:26890368-26890369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560502026	chr6:26890383-26890384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138118895	chr6:26890444-26890445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551665030	chr6:26890460-26890461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201797931	chr6:26890537-26890538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9393770	chr6:26890575-26890576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370547083	chr6:26890630-26890631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530681952	chr6:26890634-26890635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10946870	chr6:26890635-26890636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs567346193	chr6:26890809-26890810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183534300	chr6:26890866-26890867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552528130	chr6:26890888-26890889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566098396	chr6:26890892-26890893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148640653	chr6:26890900-26890901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558778987	chr6:26890936-26890937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575857309	chr6:26890972-26890973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11755326	chr6:26891044-26891045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs200383123	chr6:26891059-26891060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554914658	chr6:26891078-26891079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574856424	chr6:26891098-26891099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540767149	chr6:26891108-26891109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61052140	chr6:26891127-26891128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs11752912	chr6:26891165-26891166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs368353347	chr6:26891224-26891225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116359702	chr6:26891229-26891230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26888200-26893800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:26889400-26893600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:26889600-26891600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:26889600-26891800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:26889800-26894400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:26890200-26892800	Weak transcription	Adipose Nuclei	Adipose
7	chr6:26890200-26894400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:26890400-26893200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:26890600-26892800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:26890600-26893000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:26890600-26893000	Weak transcription	Fetal Kidney	kidney
12	chr6:26891600-26891800	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:26891800-26892200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:26891800-26893800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:26892200-26893800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:26911600-26912600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:26914200-26914800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:26922000-26923000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:26922800-26923000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:26922800-26923000	Enhancers	K562	blood
21	chr6:26923000-26923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:26923000-26924000	Weak transcription	K562	blood
23	chr6:26923400-26925400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr6:26923800-26924000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:26923800-26924400	Active TSS	GM12878-XiMat	blood
26	chr6:26923800-26925000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:26923800-26925000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:26923800-26925000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:26923800-26925000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:26923800-26925000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:26923800-26925000	Active TSS	Left Ventricle	heart
32	chr6:26923800-26925000	Active TSS	HUVEC	blood vessel
33	chr6:26923800-26925200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:26923800-26925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:26923800-26925200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:26923800-26925400	Active TSS	H1 Cell Line	embryonic stem cell
37	chr6:26923800-26925400	Active TSS	H9 Cell Line	embryonic stem cell
38	chr6:26923800-26925400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:26923800-26925400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:26923800-26925400	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr6:26923800-26925400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:26923800-26925400	Active TSS	Brain Anterior Caudate	brain
43	chr6:26923800-26925400	Active TSS	Brain Cingulate Gyrus	brain
44	chr6:26923800-26925400	Active TSS	Right Ventricle	heart
45	chr6:26923800-26925400	Active TSS	Stomach Smooth Muscle	stomach
46	chr6:26923800-26925400	Active TSS	NHDF-Ad	bronchial
47	chr6:26923800-26925600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:26923800-26925600	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr6:26923800-26925600	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr6:26923800-26925600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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