Variant report

Variant	esv16014
Chromosome Location	chr10:22609123-22617566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:878)
CpG islands
(count:1159)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:22614713-22614909	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:22612813-22613008	K562	blood:	n/a	n/a
3	ARID3A	chr10:22608889-22609254	K562	blood:	n/a	n/a
4	ARID3A	chr10:22610216-22610330	K562	blood:	n/a	n/a
5	ATF3	chr10:22609854-22609961	GM12878	blood:	n/a	n/a
6	ATF3	chr10:22609729-22610026	K562	blood:	n/a	n/a
7	BACH1	chr10:22612751-22612784	K562	blood:	n/a	n/a
8	BACH1	chr10:22610158-22610554	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:22609291-22609369	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:22614188-22614449	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr10:22609645-22609977	GM12878	blood:	n/a	n/a
12	BCLAF1	chr10:22610094-22610603	K562	blood:	n/a	chr10:22610456-22610469
13	BCLAF1	chr10:22610191-22610611	GM12878	blood:	n/a	chr10:22610456-22610469
14	BHLHE40	chr10:22614564-22615037	K562	blood:	n/a	n/a
15	BHLHE40	chr10:22609705-22610556	K562	blood:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
16	BHLHE40	chr10:22614580-22615000	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:22609687-22610491	GM12878	blood:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
18	BHLHE40	chr10:22609684-22610598	HepG2	liver:	n/a	chr10:22609956-22609965 chr10:22609957-22609966 chr10:22609956-22609965 chr10:22610460-22610476
19	BHLHE40	chr10:22608967-22609443	K562	blood:	n/a	n/a
20	BHLHE40	chr10:22614587-22615037	HepG2	liver:	n/a	n/a
21	BRCA1	chr10:22611344-22611388	GM12878	blood:	n/a	n/a
22	BRCA1	chr10:22610391-22610555	Hela-S3	cervix:	n/a	n/a
23	CCNT2	chr10:22609289-22610631	K562	blood:	n/a	chr10:22609886-22609895
24	CCNT2	chr10:22610868-22611143	K562	blood:	n/a	n/a
25	CCNT2	chr10:22614266-22614914	K562	blood:	n/a	n/a
26	CEBPB	chr10:22614643-22614679	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr10:22610100-22610453	HepG2	liver:	n/a	n/a
28	CEBPD	chr10:22609518-22610057	HepG2	liver:	n/a	n/a
29	CHD1	chr10:22611027-22611142	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr10:22610387-22610472	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr10:22610189-22610647	GM12878	blood:	n/a	chr10:22610600-22610610
32	CHD1	chr10:22609087-22609372	GM12878	blood:	n/a	n/a
33	CHD1	chr10:22614681-22615136	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr10:22614646-22615120	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr10:22609744-22610623	K562	blood:	n/a	chr10:22610600-22610610
36	CHD2	chr10:22614608-22615105	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr10:22609604-22610602	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr10:22611112-22611420	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr10:22609995-22610519	GM12878	blood:	n/a	n/a
40	CHD2	chr10:22611088-22611146	K562	blood:	n/a	n/a
41	CHD2	chr10:22609755-22610542	HepG2	liver:	n/a	n/a
42	CHD2	chr10:22614020-22614324	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr10:22610190-22610433	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr10:22609669-22610636	K562	blood:	n/a	n/a
45	CREB1	chr10:22614256-22614470	A549	lung:	n/a	n/a
46	CREB1	chr10:22614577-22614933	A549	lung:	n/a	n/a
47	CREB1	chr10:22609539-22610672	A549	lung:	n/a	n/a
48	CREB1	chr10:22609539-22610713	HepG2	liver:	n/a	n/a
49	CTBP2	chr10:22614150-22615035	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr10:22609743-22609891	GM12892	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:22613360-22613410	AG04450	lung:	fetal
2	chr10:22614933-22614983	AG04449	skin:	fetal
3	chr10:22614444-22614494	AoSMC	blood vessel:	n/a
4	chr10:22609998-22610048	ProgFib	skin:	n/a
5	chr10:22614872-22614922	HPAEpiC	pulmonary alveolar:	n/a
6	chr10:22609266-22609316	SKMC	muscle:	n/a
7	chr10:22615839-22615889	SAEC	small airway:	n/a
8	chr10:22614933-22614983	AG09319	gingival:	n/a
9	chr10:22614276-22614326	U87	brain:	n/a
10	chr10:22609903-22609953	SAEC	small airway:	n/a
11	chr10:22614694-22614744	HRE	kidney:	n/a
12	chr10:22614694-22614744	ECC-1	luminal epithelium:	n/a
13	chr10:22614444-22614494	HepG2	liver:	n/a
14	chr10:22609266-22609316	A549	lung:	n/a
15	chr10:22609266-22609316	Jurkat	blood:	n/a
16	chr10:22609629-22609679	HMEC	breast:	n/a
17	chr10:22609897-22609947	AG10803	skin:	n/a
18	chr10:22614444-22614494	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:22609897-22609947	HNPCEpiC	eye:	n/a
20	chr10:22612797-22612847	HL-60	blood:	n/a
21	chr10:22612797-22612847	GM12878	blood:	n/a
22	chr10:22609903-22609953	GM12878	blood:	n/a
23	chr10:22610507-22610557	H1-hESC	embryonic stem cell:	embryo
24	chr10:22615540-22615590	A549	lung:	n/a
25	chr10:22609629-22609679	GM12892	blood:	n/a
26	chr10:22610048-22610098	AG09319	gingival:	n/a
27	chr10:22615540-22615590	GM12878	blood:	n/a
28	chr10:22609903-22609953	HCM	heart:	n/a
29	chr10:22614444-22614494	PrEC	prostate:	n/a
30	chr10:22609897-22609947	Jurkat	blood:	n/a
31	chr10:22614694-22614744	HRCEpiC	kidney:	n/a
32	chr10:22609629-22609679	AG04450	lung:	fetal
33	chr10:22614444-22614494	U87	brain:	n/a
34	chr10:22609266-22609316	AG04450	lung:	fetal
35	chr10:22615839-22615889	U87	brain:	n/a
36	chr10:22614694-22614744	BE2_C	brain:	n/a
37	chr10:22614872-22614922	CMK	blood:	n/a
38	chr10:22612797-22612847	K562	blood:	n/a
39	chr10:22609897-22609947	GM19239	blood:	n/a
40	chr10:22610048-22610098	AG09309	skin:	n/a
41	chr10:22614933-22614983	Jurkat	blood:	n/a
42	chr10:22609629-22609679	NH-A	brain:	n/a
43	chr10:22614276-22614326	SK-N-MC	brain:	n/a
44	chr10:22611454-22611504	SK-N-SH	brain:	n/a
45	chr10:22614933-22614983	HPAEpiC	pulmonary alveolar:	n/a
46	chr10:22609994-22610044	HL-60	blood:	n/a
47	chr10:22610048-22610098	HUVEC	blood vessel:	n/a
48	chr10:22614444-22614494	CMK	blood:	n/a
49	chr10:22613360-22613410	HNPCEpiC	eye:	n/a
50	chr10:22614694-22614744	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:22291600..22293553-chr10:22610568..22612192,2	K562	blood:
2	chr10:22611886..22615757-chr10:22677839..22683321,7	K562	blood:
3	chr10:22290827..22293149-chr10:22614587..22616930,2	MCF-7	breast:
4	chr10:22608172..22617536-chr10:22624000..22632852,24	MCF-7	breast:
5	chr10:22482647..22484214-chr10:22607609..22609928,2	K562	blood:
6	chr10:21784438..21786291-chr10:22610167..22612882,2	MCF-7	breast:
7	chr10:22614751..22615680-chr20:25604638..25605211,2	Hela-S3	cervix:
8	chr10:22289174..22294396-chr10:22603847..22611692,9	K562	blood:
9	chr10:22270244..22271774-chr10:22607853..22610066,2	K562	blood:
10	chr10:22263916..22265967-chr10:22612361..22613889,2	K562	blood:
11	chr10:22607419..22609653-chr10:22662165..22664852,2	K562	blood:
12	chr10:22299957..22302551-chr10:22608056..22610053,2	MCF-7	breast:
13	chr10:22290878..22294421-chr10:22605485..22610213,6	K562	blood:
14	chr10:22288734..22294902-chr10:22609249..22612882,8	MCF-7	breast:
15	chr10:22614179..22617012-chr10:22679231..22681759,3	K562	blood:
16	chr10:22290732..22293917-chr10:22611433..22614799,4	MCF-7	breast:
17	chr10:22608209..22609987-chr10:22717593..22719148,2	MCF-7	breast:
18	chr10:22612181..22614274-chr10:22689141..22690829,2	K562	blood:
19	chr10:22536525..22546833-chr10:22602936..22612723,20	MCF-7	breast:
20	chr10:22611957..22613546-chr10:22673769..22676392,2	K562	blood:
21	chr10:21760699..21762516-chr10:22607604..22609933,2	MCF-7	breast:
22	chr10:22606981..22611063-chr10:23000780..23004970,4	K562	blood:
23	chr10:21823004..21824663-chr10:22608853..22611559,3	K562	blood:
24	chr10:22607781..22611461-chr10:22678220..22681015,4	K562	blood:
25	chr10:22611719..22614373-chr10:22717545..22719885,2	K562	blood:
26	chr10:22608333..22611559-chr10:22678806..22682635,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMI1-3	chr10:22615360-22615450	NONHSAT011742
2	lnc-BMI1-3	chr10:22614862-22615005	NONHSAT011745
3	lnc-BMI1-3	chr10:22615360-22615760	NONHSAT011745

No data

Variant related genes	Relation type
BMI1	TF binding region
ENSG00000272516	TF binding region
BMI1	CpG island
ENSG00000272516	CpG island
ENSG00000213742	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000150867	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000261671	chromatin interactions
ENSG00000204682	chromatin interactions
ENSG00000078403	chromatin interactions
ENSG00000077327	chromatin interactions
ENSG00000272366	chromatin interactions
ENSG00000136770	chromatin interactions

Extended variants
information (count: 281 )
Associated
traits (count: 37 )

Variant overlapped rSNPs/rCNVs (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	rs532381947	chr10:22609415-22609416	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs552077176	chr10:22609562-22609563	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs182254928	chr10:22609598-22609599	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs112770685	chr10:22609752-22609753	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs537926041	chr10:22609779-22609780	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs548196825	chr10:22609839-22609840	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs568077631	chr10:22609842-22609843	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	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
26	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
27	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
28	rs535682939	chr10:22610221-22610222	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs556459744	chr10:22610298-22610299	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs377124330	chr10:22610320-22610321	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs575435431	chr10:22610353-22610354	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs544290661	chr10:22610362-22610363	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs561723968	chr10:22610365-22610366	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs377088103	chr10:22610423-22610424	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs554616218	chr10:22610468-22610469	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs574438684	chr10:22610514-22610515	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs140173439	chr10:22610535-22610536	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs555539462	chr10:22610591-22610592	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs532290569	chr10:22610987-22610988	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs547480839	chr10:22610999-22611000	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs575574636	chr10:22611007-22611008	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs377219284	chr10:22611031-22611032	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs546005987	chr10:22611165-22611166	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs562313946	chr10:22611192-22611193	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs545284603	chr10:22611194-22611195	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs544504419	chr10:22611231-22611232	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs531706447	chr10:22611278-22611279	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs548235395	chr10:22611310-22611311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs568114465	chr10:22611322-22611323	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs370178514	chr10:22611323-22611324	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 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:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr10:22606200-22609200	Weak transcription	Colonic Mucosa	Colon
4	chr10:22606200-22609200	Weak transcription	Esophagus	oesophagus
5	chr10:22606200-22609200	Weak transcription	Lung	lung
6	chr10:22606200-22609200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr10:22606400-22609400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr10:22608600-22609200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
9	chr10:22608600-22609200	Enhancers	Small Intestine	intestine
10	chr10:22608600-22609200	Flanking Active TSS	K562	blood
11	chr10:22608600-22609400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr10:22608600-22609400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
13	chr10:22608600-22609400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:22608600-22609400	Bivalent Enhancer	Fetal Thymus	thymus
15	chr10:22608600-22609400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr10:22608800-22609200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:22608800-22609200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:22608800-22609200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr10:22608800-22609200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:22608800-22609200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr10:22608800-22609200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr10:22608800-22609200	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
23	chr10:22608800-22609200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
24	chr10:22608800-22609200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr10:22608800-22609200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr10:22608800-22609200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr10:22608800-22609200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr10:22608800-22609200	Flanking Active TSS	Fetal Intestine Small	intestine
29	chr10:22608800-22609200	Flanking Active TSS	Fetal Kidney	kidney
30	chr10:22608800-22609200	Enhancers	Left Ventricle	heart
31	chr10:22608800-22609200	Enhancers	Pancreas	Pancrea
32	chr10:22608800-22609200	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr10:22608800-22609200	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr10:22608800-22609200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr10:22608800-22609200	Flanking Active TSS	A549	lung
36	chr10:22608800-22609200	Flanking Active TSS	Hela-S3	cervix
37	chr10:22608800-22609200	Enhancers	HSMM	muscle
38	chr10:22608800-22609200	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
39	chr10:22608800-22609400	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr10:22608800-22609400	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr10:22608800-22609400	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr10:22608800-22609400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr10:22608800-22609400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr10:22608800-22609400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
45	chr10:22608800-22609400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr10:22608800-22609400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:22608800-22609400	Flanking Active TSS	Liver	Liver
48	chr10:22608800-22609400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr10:22608800-22609400	Active TSS	Brain Substantia Nigra	brain
50	chr10:22608800-22609400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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