Variant report

Variant	nsv874284
Chromosome Location	chr2:74283728-74348797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1647)
CpG islands
(count:978)
Chromatin interactive
region (count:135)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:74347280-74347554	K562	blood:	n/a	n/a
2	ARID3A	chr2:74305588-74305999	K562	blood:	n/a	n/a
3	ARID3A	chr2:74299790-74300099	K562	blood:	n/a	n/a
4	ARID3A	chr2:74304720-74304919	K562	blood:	n/a	n/a
5	ARID3A	chr2:74310981-74311325	K562	blood:	n/a	n/a
6	ARID3A	chr2:74347379-74347718	HepG2	liver:	n/a	n/a
7	ATF1	chr2:74305703-74305867	K562	blood:	n/a	n/a
8	ATF2	chr2:74306899-74307749	GM12878	blood:	n/a	n/a
9	ATF2	chr2:74306816-74307590	GM12878	blood:	n/a	n/a
10	ATF2	chr2:74347237-74347765	GM12878	blood:	n/a	n/a
11	BACH1	chr2:74287279-74287292	K562	blood:	n/a	n/a
12	BACH1	chr2:74335966-74335967	K562	blood:	n/a	n/a
13	BACH1	chr2:74347355-74347565	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:74304887-74304962	K562	blood:	n/a	n/a
15	BATF	chr2:74306858-74307395	GM12878	blood:	n/a	n/a
16	BATF	chr2:74307008-74307420	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:74307204-74307417	GM12878	blood:	n/a	chr2:74307312-74307321
18	BCL11A	chr2:74307011-74307472	GM12878	blood:	n/a	chr2:74307312-74307321
19	BCL3	chr2:74306987-74307444	GM12878	blood:	n/a	chr2:74307312-74307321
20	BCLAF1	chr2:74347160-74347932	GM12878	blood:	n/a	chr2:74347733-74347746 chr2:74347330-74347343 chr2:74347735-74347744
21	BCLAF1	chr2:74347228-74347746	GM12878	blood:	n/a	chr2:74347733-74347746 chr2:74347330-74347343 chr2:74347735-74347744
22	BCLAF1	chr2:74306773-74307811	GM12878	blood:	n/a	chr2:74307312-74307321
23	BCLAF1	chr2:74306854-74307506	GM12878	blood:	n/a	chr2:74307312-74307321
24	BHLHE40	chr2:74302868-74303157	K562	blood:	n/a	n/a
25	BHLHE40	chr2:74347088-74347715	GM12878	blood:	n/a	chr2:74347325-74347341
26	BHLHE40	chr2:74306910-74307621	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:74304811-74305056	K562	blood:	n/a	n/a
28	BHLHE40	chr2:74310902-74311326	K562	blood:	n/a	n/a
29	BHLHE40	chr2:74306970-74307169	K562	blood:	n/a	n/a
30	BHLHE40	chr2:74347357-74347932	K562	blood:	n/a	n/a
31	BRCA1	chr2:74347412-74348008	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr2:74347810-74347811	HepG2	liver:	n/a	n/a
33	BRCA1	chr2:74334388-74334531	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr2:74310722-74311375	K562	blood:	n/a	n/a
35	CBX3	chr2:74347272-74348002	K562	blood:	n/a	n/a
36	CBX3	chr2:74346961-74348184	K562	blood:	n/a	n/a
37	CCNT2	chr2:74310892-74311321	K562	blood:	n/a	n/a
38	CCNT2	chr2:74347309-74347794	K562	blood:	n/a	n/a
39	CCNT2	chr2:74304831-74305138	K562	blood:	n/a	n/a
40	CEBPB	chr2:74298613-74298860	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:74299703-74299900	K562	blood:	n/a	chr2:74299793-74299804
42	CEBPB	chr2:74286305-74286522	A549	lung:	n/a	chr2:74286435-74286446
43	CEBPB	chr2:74299631-74300032	K562	blood:	n/a	chr2:74299793-74299804
44	CEBPB	chr2:74286313-74286482	K562	blood:	n/a	chr2:74286435-74286446
45	CEBPB	chr2:74290645-74290985	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:74299666-74299988	HepG2	liver:	n/a	chr2:74299793-74299804
47	CEBPB	chr2:74294513-74294833	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:74348345-74348635	A549	lung:	n/a	chr2:74348488-74348499
49	CEBPB	chr2:74294494-74294828	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:74296671-74296912	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:74334539-74334589	NH-A	brain:	n/a
2	chr2:74347435-74347485	ProgFib	skin:	n/a
3	chr2:74334539-74334589	NH-A	brain:	n/a
4	chr2:74347435-74347485	ProgFib	skin:	n/a
5	chr2:74287435-74287485	HCF	heart:	n/a
6	chr2:74308468-74308518	BE2_C	brain:	n/a
7	chr2:74332041-74332091	RPTEC	kidney:	n/a
8	chr2:74329082-74329132	NB4	blood:	n/a
9	chr2:74347215-74347265	MCF-7	breast:	n/a
10	chr2:74348255-74348305	SK-N-SH	brain:	n/a
11	chr2:74347274-74347324	HCM	heart:	n/a
12	chr2:74329833-74329883	HCPEpiC	choroid plexus:	n/a
13	chr2:74328923-74328973	SK-N-SH	brain:	n/a
14	chr2:74287435-74287485	LNCaP	prostate:	n/a
15	chr2:74332041-74332091	HRPEpiC	eye:	n/a
16	chr2:74347616-74347666	HEEpiC	esophagus:	n/a
17	chr2:74329833-74329883	ECC-1	luminal epithelium:	n/a
18	chr2:74329082-74329132	HNPCEpiC	eye:	n/a
19	chr2:74334539-74334589	SKMC	muscle:	n/a
20	chr2:74287435-74287485	HNPCEpiC	eye:	n/a
21	chr2:74348255-74348305	MCF10A-Er-Src	breast:	n/a
22	chr2:74347215-74347265	A549	lung:	n/a
23	chr2:74308468-74308518	ovcar-3	ovarian:	n/a
24	chr2:74329809-74329859	IMR90	lung:	fetal
25	chr2:74332041-74332091	HCF	heart:	n/a
26	chr2:74308468-74308518	SK-N-SH	brain:	n/a
27	chr2:74348255-74348305	ECC-1	luminal epithelium:	n/a
28	chr2:74329332-74329382	Hela-S3	cervix:	n/a
29	chr2:74329332-74329382	NHDF-neo	bronchial:	n/a
30	chr2:74347616-74347666	HepG2	liver:	n/a
31	chr2:74332041-74332091	GM12892	blood:	n/a
32	chr2:74347435-74347485	HCPEpiC	choroid plexus:	n/a
33	chr2:74329082-74329132	HL-60	blood:	n/a
34	chr2:74348255-74348305	AG04449	skin:	fetal
35	chr2:74334539-74334589	SAEC	small airway:	n/a
36	chr2:74347616-74347666	Jurkat	blood:	n/a
37	chr2:74287435-74287485	T-47D	breast:	n/a
38	chr2:74347435-74347485	AG10803	skin:	n/a
39	chr2:74287435-74287485	BE2_C	brain:	n/a
40	chr2:74328923-74328973	AG09309	skin:	n/a
41	chr2:74347215-74347265	HUVEC	blood vessel:	n/a
42	chr2:74334539-74334589	GM12891	blood:	n/a
43	chr2:74347616-74347666	SAEC	small airway:	n/a
44	chr2:74347616-74347666	AG04449	skin:	fetal
45	chr2:74347616-74347666	HRPEpiC	eye:	n/a
46	chr2:74346210-74346260	SK-N-SH	brain:	n/a
47	chr2:74287435-74287485	HCPEpiC	choroid plexus:	n/a
48	chr2:74287435-74287485	CMK	blood:	n/a
49	chr2:74329082-74329132	HepG2	liver:	n/a
50	chr2:74308468-74308518	MCF-7	breast:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:74210805..74212342-chr2:74309790..74311328,2	MCF-7	breast:
2	chr2:74285707..74287779-chr2:74292487..74295253,2	K562	blood:
3	chr16:2204962..2205609-chr2:74347432..74348083,2	Hela-S3	cervix:
4	chr2:74311799..74313643-chr2:74317613..74320448,2	K562	blood:
5	chr2:74282003..74283717-chr2:74291378..74294000,2	MCF-7	breast:
6	chr2:74303366..74305130-chr2:74308677..74311311,2	K562	blood:
7	chr2:74210918..74213752-chr2:74338111..74340312,2	MCF-7	breast:
8	chr2:74077294..74080205-chr2:74346163..74349130,2	K562	blood:
9	chr2:74228214..74230441-chr2:74345373..74347359,2	MCF-7	breast:
10	chr2:74211205..74213910-chr2:74316138..74318020,2	MCF-7	breast:
11	chr2:74230315..74232342-chr2:74308990..74310979,2	K562	blood:
12	chr2:74234336..74236088-chr2:74326202..74328646,2	MCF-7	breast:
13	chr2:74330613..74332163-chr2:74332927..74334673,2	K562	blood:
14	chr2:74290589..74292591-chr2:74294386..74296993,2	K562	blood:
15	chr2:74296493..74298697-chr2:74301422..74303522,3	K562	blood:
16	chr2:74331300..74332894-chr2:74335535..74338121,2	MCF-7	breast:
17	chr2:74209017..74213063-chr2:74345530..74349441,7	MCF-7	breast:
18	chr2:74328812..74330773-chr2:74332482..74334239,2	K562	blood:
19	chr2:74335555..74337935-chr2:74348747..74350804,2	MCF-7	breast:
20	chr2:74210336..74213220-chr2:74335043..74337210,3	MCF-7	breast:
21	chr2:74326343..74328844-chr2:74352521..74354991,2	MCF-7	breast:
22	chr2:74263750..74267356-chr2:74281436..74283825,3	K562	blood:
23	chr2:74247578..74249346-chr2:74314396..74316715,2	MCF-7	breast:
24	chr2:74187721..74190060-chr2:74320133..74322704,2	K562	blood:
25	chr2:74300915..74302762-chr2:74304930..74307644,3	K562	blood:
26	chr2:74210985..74213488-chr2:74306326..74309716,4	MCF-7	breast:
27	chr2:74211058..74214577-chr2:74295216..74297710,3	MCF-7	breast:
28	chr2:74154400..74156910-chr2:74330395..74332321,2	MCF-7	breast:
29	chr2:74153590..74155495-chr2:74346048..74348829,2	MCF-7	breast:
30	chr2:74209051..74213091-chr2:74319558..74323608,5	MCF-7	breast:
31	chr2:74218371..74220942-chr2:74324790..74327724,2	MCF-7	breast:
32	chr2:74345218..74347575-chr2:74362895..74365930,3	MCF-7	breast:
33	chr2:74283509..74286294-chr20:62151875..62153766,2	MCF-7	breast:
34	chr2:74346117..74347922-chr2:74374665..74375603,8	MCF-7	breast:
35	chr2:74346058..74349268-chr2:74424477..74426947,5	K562	blood:
36	chr2:74211163..74212719-chr2:74332810..74334691,2	MCF-7	breast:
37	chr2:74336985..74342809-chr2:74343895..74348590,10	MCF-7	breast:
38	chr2:74211836..74213595-chr2:74326351..74328832,2	MCF-7	breast:
39	chr2:74313056..74315941-chr2:74327594..74329312,2	K562	blood:
40	chr2:74347130..74350614-chr2:74373490..74375151,4	K562	blood:
41	chr2:74214395..74216353-chr2:74293422..74296329,2	MCF-7	breast:
42	chr2:74314378..74316915-chr2:74318069..74319795,2	MCF-7	breast:
43	chr2:74336308..74342547-chr2:74345865..74348984,6	K562	blood:
44	chr2:74302146..74304941-chr2:74345913..74348314,2	K562	blood:
45	chr2:74213085..74215913-chr2:74284543..74286784,2	MCF-7	breast:
46	chr2:74335713..74338068-chr2:74339184..74340724,2	MCF-7	breast:
47	chr2:74290589..74292591-chr2:74294386..74296993,2	K562	blood:
48	chr2:74299880..74303029-chr2:74304930..74306783,3	K562	blood:
49	chr2:74275740..74280453-chr2:74282056..74286021,5	K562	blood:
50	chr2:74215681..74218530-chr2:74336371..74337878,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073263.1-3	chr2:74345408-74349576	NONHSAT071660
2	lnc-AC073263.1-4	chr2:74297190-74298172	ncRnaDb_ncrna_FR186324_1
3	lnc-AC073263.1-3	chr2:74347807-74349577	NONHSAT071661

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TET3	hsa-miR-26b-5p	chr2:74334896-74334917
2	TET3	hsa-miR-98-5p	chr2:74331325-74331348
3	TET3	hsa-miR-98-5p	chr2:74332077-74332101
4	TET3	hsa-miR-26b-5p	chr2:74334860-74334880

Variant related genes	Relation type
FNBP1P1	TF binding region
FNBP1P1	CpG island
ENSG00000206630	chromatin interactions
ENSG00000255989	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000125534	chromatin interactions
ENSG00000187605	chromatin interactions
ENSG00000217702	chromatin interactions
ENSG00000204843	chromatin interactions
ENSG00000203711	chromatin interactions
ENSG00000257800	chromatin interactions
ENSG00000225439	chromatin interactions
ENSG00000065911	chromatin interactions
ENSG00000235499	chromatin interactions
ENSG00000114978	chromatin interactions
ENSG00000114956	chromatin interactions
ENSG00000163170	chromatin interactions
ENSG00000237883	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000124356	chromatin interactions

Extended variants
information (count: 2777 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2777 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6745236	chr2:74283728-74283729	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572085645	chr2:74283743-74283744	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183319005	chr2:74283744-74283745	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554540289	chr2:74283756-74283757	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528538638	chr2:74283768-74283769	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563355054	chr2:74283876-74283877	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541405079	chr2:74283905-74283906	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546707126	chr2:74283918-74283919	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544049897	chr2:74283936-74283937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565491470	chr2:74283959-74283960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188107005	chr2:74283977-74283978	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs6745792	chr2:74284033-74284034	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs367920923	chr2:74284140-74284141	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541561495	chr2:74284141-74284142	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543421990	chr2:74284205-74284206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559918135	chr2:74284357-74284358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530199386	chr2:74284372-74284373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145161161	chr2:74284410-74284411	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563651234	chr2:74284434-74284435	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75125312	chr2:74284444-74284445	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs549630444	chr2:74284470-74284471	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555821014	chr2:74284510-74284511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574096906	chr2:74284530-74284531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571128992	chr2:74284535-74284536	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532203149	chr2:74284563-74284564	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138960184	chr2:74284686-74284687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs10200470	chr2:74284687-74284688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs191326005	chr2:74284709-74284710	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs559733463	chr2:74284746-74284747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149399759	chr2:74284755-74284756	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs182353212	chr2:74284767-74284768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs533583767	chr2:74284777-74284778	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs568075666	chr2:74284825-74284826	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs559268001	chr2:74284843-74284844	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs117604874	chr2:74284844-74284845	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371751630	chr2:74284883-74284884	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541684452	chr2:74284892-74284893	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553527312	chr2:74284920-74284921	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs545687176	chr2:74284926-74284927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574837162	chr2:74284966-74284967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs542265627	chr2:74284967-74284968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs186621437	chr2:74284981-74284982	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375096867	chr2:74284990-74284991	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs192532454	chr2:74285085-74285086	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs60800561	chr2:74285110-74285111	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs531289643	chr2:74285126-74285127	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs184522736	chr2:74285133-74285134	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs79322771	chr2:74285147-74285148	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs10179742	chr2:74285160-74285161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs565821167	chr2:74285213-74285214	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74264800-74311000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:74265000-74300600	Weak transcription	Fetal Brain Male	brain
3	chr2:74265400-74315000	Weak transcription	HUVEC	blood vessel
4	chr2:74266400-74287200	Weak transcription	HSMM	muscle
5	chr2:74269000-74300200	Weak transcription	Fetal Kidney	kidney
6	chr2:74269800-74328000	Weak transcription	Psoas Muscle	Psoas
7	chr2:74271600-74287600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr2:74272800-74285600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr2:74273000-74285000	Weak transcription	HMEC	breast
10	chr2:74273200-74293800	Weak transcription	Fetal Lung	lung
11	chr2:74274400-74286400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:74275200-74307800	Weak transcription	Aorta	Aorta
13	chr2:74275600-74285800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:74275600-74304000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:74275800-74301400	Weak transcription	A549	lung
16	chr2:74275800-74301600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr2:74275800-74307800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr2:74275800-74317000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr2:74276000-74285800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr2:74276000-74294800	Weak transcription	Right Ventricle	heart
21	chr2:74276200-74307600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:74276600-74284000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr2:74276600-74286000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:74276600-74293600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr2:74276600-74293800	Weak transcription	Fetal Brain Female	brain
26	chr2:74276600-74294800	Weak transcription	Lung	lung
27	chr2:74276800-74285200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:74276800-74286800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr2:74276800-74300800	Weak transcription	Liver	Liver
30	chr2:74276800-74307400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:74277000-74284000	Weak transcription	Esophagus	oesophagus
32	chr2:74277000-74287400	Weak transcription	Gastric	stomach
33	chr2:74277000-74291600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:74277000-74291800	Weak transcription	NHLF	lung
35	chr2:74277000-74307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr2:74277000-74308000	Weak transcription	Adipose Nuclei	Adipose
37	chr2:74277200-74301200	Weak transcription	HepG2	liver
38	chr2:74277200-74302600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:74277200-74307600	Weak transcription	Spleen	Spleen
40	chr2:74277200-74307600	Weak transcription	Hela-S3	cervix
41	chr2:74277400-74286800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr2:74277600-74300200	Weak transcription	NHEK	skin
43	chr2:74277600-74306800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr2:74277800-74286800	Weak transcription	Stomach Mucosa	stomach
45	chr2:74278400-74285200	Weak transcription	Fetal Intestine Large	intestine
46	chr2:74278400-74285800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr2:74278400-74285800	Weak transcription	Brain Germinal Matrix	brain
48	chr2:74278400-74286400	Weak transcription	Fetal Stomach	stomach
49	chr2:74279200-74293800	Weak transcription	Fetal Muscle Leg	muscle
50	chr2:74279200-74317000	Weak transcription	Small Intestine	intestine

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