Variant report

Variant	esv3342642
Chromosome Location	chr10:22608771-22612319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:605)
CpG islands
(count:732)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:22608889-22609254	K562	blood:	n/a	n/a
2	ARID3A	chr10:22610216-22610330	K562	blood:	n/a	n/a
3	ATF3	chr10:22609729-22610026	K562	blood:	n/a	n/a
4	ATF3	chr10:22609854-22609961	GM12878	blood:	n/a	n/a
5	BACH1	chr10:22609291-22609369	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:22610158-22610554	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr10:22609645-22609977	GM12878	blood:	n/a	n/a
8	BCLAF1	chr10:22610094-22610603	K562	blood:	n/a	chr10:22610456-22610469
9	BCLAF1	chr10:22610191-22610611	GM12878	blood:	n/a	chr10:22610456-22610469
10	BHLHE40	chr10:22609705-22610556	K562	blood:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
11	BHLHE40	chr10:22609687-22610491	GM12878	blood:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
12	BHLHE40	chr10:22608967-22609443	K562	blood:	n/a	n/a
13	BHLHE40	chr10:22609684-22610598	HepG2	liver:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
14	BRCA1	chr10:22611344-22611388	GM12878	blood:	n/a	n/a
15	BRCA1	chr10:22610391-22610555	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr10:22610868-22611143	K562	blood:	n/a	n/a
17	CCNT2	chr10:22609289-22610631	K562	blood:	n/a	chr10:22609886-22609895
18	CEBPD	chr10:22609518-22610057	HepG2	liver:	n/a	n/a
19	CEBPD	chr10:22610100-22610453	HepG2	liver:	n/a	n/a
20	CHD1	chr10:22610387-22610472	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr10:22611027-22611142	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr10:22609087-22609372	GM12878	blood:	n/a	n/a
23	CHD1	chr10:22610189-22610647	GM12878	blood:	n/a	chr10:22610600-22610610
24	CHD2	chr10:22611112-22611420	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr10:22609995-22610519	GM12878	blood:	n/a	n/a
26	CHD2	chr10:22610190-22610433	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr10:22609744-22610623	K562	blood:	n/a	chr10:22610600-22610610
28	CHD2	chr10:22611088-22611146	K562	blood:	n/a	n/a
29	CHD2	chr10:22609755-22610542	HepG2	liver:	n/a	n/a
30	CHD2	chr10:22609604-22610602	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr10:22609539-22610672	A549	lung:	n/a	n/a
32	CREB1	chr10:22609669-22610636	K562	blood:	n/a	n/a
33	CREB1	chr10:22609539-22610713	HepG2	liver:	n/a	n/a
34	CTCF	chr10:22609517-22609845	GM19240	blood:	n/a	n/a
35	CTCF	chr10:22609743-22609891	GM12892	blood:	n/a	n/a
36	CTCF	chr10:22610472-22610533	Fibrobl	skin:	n/a	n/a
37	CTCF	chr10:22609749-22609907	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:22611200-22611350	BJ	skin:	n/a	n/a
39	CTCF	chr10:22610460-22610610	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr10:22610480-22610630	GM12873	blood:	n/a	n/a
41	CTCF	chr10:22609758-22609888	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:22609740-22609890	GM12865	blood:	n/a	n/a
43	CTCF	chr10:22608632-22609164	K562	blood:	n/a	n/a
44	CTCF	chr10:22609791-22609839	A549	lung:	n/a	n/a
45	CTCF	chr10:22610180-22610330	GM06990	blood:	n/a	n/a
46	CTCF	chr10:22609759-22609913	GM19238	blood:	n/a	n/a
47	CTCF	chr10:22609700-22609850	GM12874	blood:	n/a	n/a
48	CTCF	chr10:22609740-22609890	GM12869	blood:	n/a	n/a
49	CTCF	chr10:22609573-22609676	GM19238	blood:	n/a	n/a
50	CTCF	chr10:22609590-22609653	MCF-7	breast:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:22609994-22610044	GM19239	blood:	n/a
2	chr10:22611454-22611504	GM12891	blood:	n/a
3	chr10:22611454-22611504	Hepatocyte	liver:	n/a
4	chr10:22609903-22609953	Hela-S3	cervix:	n/a
5	chr10:22611454-22611504	AG09309	skin:	n/a
6	chr10:22608858-22608908	K562	blood:	n/a
7	chr10:22609629-22609679	HMEC	breast:	n/a
8	chr10:22609994-22610044	IMR90	lung:	fetal
9	chr10:22611454-22611504	MCF10A-Er-Src	breast:	n/a
10	chr10:22609629-22609679	HIPEpiC	eye:	n/a
11	chr10:22609897-22609947	AG09319	gingival:	n/a
12	chr10:22608858-22608908	NHDF-neo	bronchial:	n/a
13	chr10:22609918-22609968	A549	lung:	n/a
14	chr10:22610048-22610098	CMK	blood:	n/a
15	chr10:22609994-22610044	BJ	skin:	n/a
16	chr10:22611454-22611504	GM12892	blood:	n/a
17	chr10:22609903-22609953	IMR90	lung:	fetal
18	chr10:22609266-22609316	GM12891	blood:	n/a
19	chr10:22609918-22609968	Caco-2	colon:	n/a
20	chr10:22609994-22610044	RPTEC	kidney:	n/a
21	chr10:22609918-22609968	HAEpiC	amniotic membrane:	n/a
22	chr10:22608951-22609001	HRPEpiC	eye:	n/a
23	chr10:22609629-22609679	GM12878	blood:	n/a
24	chr10:22609903-22609953	HAEpiC	amniotic membrane:	n/a
25	chr10:22609918-22609968	MCF10A-Er-Src	breast:	n/a
26	chr10:22609903-22609953	HEEpiC	esophagus:	n/a
27	chr10:22610507-22610557	AG04449	skin:	fetal
28	chr10:22608858-22608908	GM19239	blood:	n/a
29	chr10:22611454-22611504	AG10803	skin:	n/a
30	chr10:22610048-22610098	HCPEpiC	choroid plexus:	n/a
31	chr10:22609629-22609679	H1-hESC	embryonic stem cell:	embryo
32	chr10:22610048-22610098	GM12891	blood:	n/a
33	chr10:22610507-22610557	MCF10A-Er-Src	breast:	n/a
34	chr10:22609897-22609947	PrEC	prostate:	n/a
35	chr10:22609266-22609316	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:22609897-22609947	HRPEpiC	eye:	n/a
37	chr10:22608951-22609001	AG10803	skin:	n/a
38	chr10:22608951-22609001	AG09319	gingival:	n/a
39	chr10:22610048-22610098	K562	blood:	n/a
40	chr10:22609629-22609679	ECC-1	luminal epithelium:	n/a
41	chr10:22609918-22609968	AG09319	gingival:	n/a
42	chr10:22608951-22609001	HRCEpiC	kidney:	n/a
43	chr10:22609903-22609953	HMEC	breast:	n/a
44	chr10:22609266-22609316	AG09309	skin:	n/a
45	chr10:22609918-22609968	Hepatocyte	liver:	n/a
46	chr10:22609897-22609947	AG09309	skin:	n/a
47	chr10:22609266-22609316	ovcar-3	ovarian:	n/a
48	chr10:22609629-22609679	HEK293	kidney:	embryo
49	chr10:22609897-22609947	HIPEpiC	eye:	n/a
50	chr10:22609918-22609968	GM19239	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:22611957..22613546-chr10:22673769..22676392,2	K562	blood:
2	chr10:22606981..22611063-chr10:23000780..23004970,4	K562	blood:
3	chr10:22611719..22614373-chr10:22717545..22719885,2	K562	blood:
4	chr10:22290732..22293917-chr10:22611433..22614799,4	MCF-7	breast:
5	chr10:22608209..22609987-chr10:22717593..22719148,2	MCF-7	breast:
6	chr10:22299957..22302551-chr10:22608056..22610053,2	MCF-7	breast:
7	chr10:22291600..22293553-chr10:22610568..22612192,2	K562	blood:
8	chr10:22611886..22615757-chr10:22677839..22683321,7	K562	blood:
9	chr10:22253754..22256487-chr10:22607279..22608984,2	MCF-7	breast:
10	chr10:21760699..21762516-chr10:22607604..22609933,2	MCF-7	breast:
11	chr10:22270244..22271774-chr10:22607853..22610066,2	K562	blood:
12	chr10:21784438..21786291-chr10:22610167..22612882,2	MCF-7	breast:
13	chr10:22482647..22484214-chr10:22607609..22609928,2	K562	blood:
14	chr10:22608333..22611559-chr10:22678806..22682635,4	K562	blood:
15	chr10:22608172..22617536-chr10:22624000..22632852,24	MCF-7	breast:
16	chr10:22612181..22614274-chr10:22689141..22690829,2	K562	blood:
17	chr10:22536525..22546833-chr10:22602936..22612723,20	MCF-7	breast:
18	chr10:21823004..21824663-chr10:22608853..22611559,3	K562	blood:
19	chr10:22289174..22294396-chr10:22603847..22611692,9	K562	blood:
20	chr10:22288734..22294902-chr10:22609249..22612882,8	MCF-7	breast:
21	chr10:22290878..22294421-chr10:22605485..22610213,6	K562	blood:
22	chr10:22607419..22609653-chr10:22662165..22664852,2	K562	blood:
23	chr10:22607820..22608812-chr3:47823476..47824299,2	Hela-S3	cervix:
24	chr10:22607781..22611461-chr10:22678220..22681015,4	K562	blood:

No data

Variant related genes	Relation type
BMI1	TF binding region
BMI1	CpG island
ENSG00000078403	chromatin interactions
ENSG00000136770	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000077327	chromatin interactions
ENSG00000261671	chromatin interactions
ENSG00000150867	chromatin interactions
ENSG00000204682	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000272366	chromatin interactions

Extended variants
information (count: 103 )
Associated
traits (count: 37 )

Variant overlapped rSNPs/rCNVs (count:103 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200827649	chr10:22608771-22608772	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs561203548	chr10:22608792-22608793	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs186281665	chr10:22608795-22608796	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs546839916	chr10:22608799-22608800	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs370026480	chr10:22608813-22608814	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs74584445	chr10:22608826-22608827	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs12412271	chr10:22608829-22608830	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs146379795	chr10:22608832-22608833	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs376457351	chr10:22608835-22608836	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs369978196	chr10:22608837-22608838	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs139836993	chr10:22608855-22608856	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs377084138	chr10:22608870-22608871	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs369935672	chr10:22608921-22608922	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs10146	chr10:22608937-22608938	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs373117705	chr10:22608947-22608948	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs569248806	chr10:22608952-22608953	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs143156676	chr10:22608967-22608968	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs372592054	chr10:22608975-22608976	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs151178813	chr10:22608986-22608987	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs371850122	chr10:22609020-22609021	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs199507831	chr10:22609033-22609034	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs534193003	chr10:22609042-22609043	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs554085512	chr10:22609119-22609120	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs577323828	chr10:22609157-22609158	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs544778048	chr10:22609159-22609160	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs373585308	chr10:22609189-22609190	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs77141143	chr10:22609205-22609206	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs575398175	chr10:22609234-22609235	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs550066058	chr10:22609236-22609237	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs188987005	chr10:22609260-22609261	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs113465081	chr10:22609271-22609272	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs557638519	chr10:22609272-22609273	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs202186699	chr10:22609273-22609274	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs60234884	chr10:22609274-22609275	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs560842242	chr10:22609282-22609283	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs530033102	chr10:22609289-22609290	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs567010024	chr10:22609295-22609296	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs376472076	chr10:22609296-22609297	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs72814833	chr10:22609331-22609332	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372435441	chr10:22609353-22609354	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs532381947	chr10:22609415-22609416	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs552077176	chr10:22609562-22609563	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs182254928	chr10:22609598-22609599	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs112770685	chr10:22609752-22609753	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs537926041	chr10:22609779-22609780	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs548196825	chr10:22609839-22609840	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs568077631	chr10:22609842-22609843	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs201869716	chr10:22610088-22610089	Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs554395283	chr10:22610154-22610155	Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs577461106	chr10:22610180-22610181	Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:37)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	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
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22605400-22609400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:22605800-22610000	Weak transcription	Spleen	Spleen
3	chr10:22606200-22608800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr10:22606200-22608800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr10:22606200-22608800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:22606200-22608800	Weak transcription	Left Ventricle	heart
7	chr10:22606200-22608800	Weak transcription	Pancreas	Pancrea
8	chr10:22606200-22608800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr10:22606200-22609000	Weak transcription	Aorta	Aorta
10	chr10:22606200-22609000	Weak transcription	Placenta	Placenta
11	chr10:22606200-22609000	Weak transcription	Fetal Stomach	stomach
12	chr10:22606200-22609000	Weak transcription	Ovary	ovary
13	chr10:22606200-22609200	Weak transcription	Colonic Mucosa	Colon
14	chr10:22606200-22609200	Weak transcription	Esophagus	oesophagus
15	chr10:22606200-22609200	Weak transcription	Lung	lung
16	chr10:22606200-22609200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr10:22606400-22608800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:22606400-22608800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr10:22606400-22608800	Weak transcription	Fetal Muscle Leg	muscle
20	chr10:22606400-22608800	Weak transcription	HSMMtube	muscle
21	chr10:22606400-22609000	Weak transcription	Brain Angular Gyrus	brain
22	chr10:22606400-22609000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr10:22606400-22609000	Weak transcription	Right Ventricle	heart
24	chr10:22606400-22609400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr10:22606600-22608800	Enhancers	Primary T cells from cord blood	blood
26	chr10:22606600-22608800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:22606600-22608800	Weak transcription	Adipose Nuclei	Adipose
28	chr10:22606600-22608800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr10:22606600-22608800	Enhancers	HepG2	liver
30	chr10:22606600-22609000	Enhancers	Fetal Intestine Large	intestine
31	chr10:22606800-22608800	Enhancers	Primary B cells from cord blood	blood
32	chr10:22606800-22608800	Weak transcription	Brain Anterior Caudate	brain
33	chr10:22607000-22608800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr10:22607000-22608800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr10:22607000-22608800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr10:22607000-22608800	Weak transcription	Brain Hippocampus Middle	brain
37	chr10:22607000-22608800	Weak transcription	Brain Substantia Nigra	brain
38	chr10:22607000-22608800	Weak transcription	Right Atrium	heart
39	chr10:22607000-22608800	Weak transcription	Stomach Mucosa	stomach
40	chr10:22607000-22608800	Weak transcription	HSMM	muscle
41	chr10:22607000-22608800	Weak transcription	NHLF	lung
42	chr10:22607000-22609000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr10:22607000-22609000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr10:22607200-22608800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:22607200-22608800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:22607200-22608800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr10:22607200-22609000	Weak transcription	NHEK	skin
48	chr10:22607400-22608800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr10:22607400-22608800	Weak transcription	Psoas Muscle	Psoas
50	chr10:22607400-22608800	Enhancers	Dnd41	blood

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