Variant report

Variant	esv3497616
Chromosome Location	chr10:1091673-1096308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:795)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1095043-1095579	K562	blood:	n/a	n/a
2	ARID3A	chr10:1094678-1095649	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:1095998-1096413	K562	blood:	n/a	n/a
4	ATF1	chr10:1094740-1095525	K562	blood:	n/a	chr10:1094969-1094983
5	ATF2	chr10:1094938-1095655	GM12878	blood:	n/a	chr10:1094969-1094983
6	ATF2	chr10:1094297-1094676	GM12878	blood:	n/a	n/a
7	ATF2	chr10:1094934-1095367	H1-hESC	embryonic stem cell:	n/a	chr10:1094969-1094983
8	ATF2	chr10:1094706-1095632	GM12878	blood:	n/a	chr10:1094969-1094983
9	BACH1	chr10:1094282-1095268	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:1093937-1094012	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:1094179-1094576	K562	blood:	n/a	n/a
12	BACH1	chr10:1095490-1095589	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr10:1094898-1095599	GM12878	blood:	n/a	n/a
14	BCL3	chr10:1094581-1095649	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
15	BCL3	chr10:1094143-1095663	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
16	BCL3	chr10:1094581-1096032	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
17	BCLAF1	chr10:1094621-1095982	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
18	BCLAF1	chr10:1094215-1095692	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
19	BHLHE40	chr10:1094091-1095724	K562	blood:	n/a	n/a
20	BHLHE40	chr10:1094164-1095673	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:1096276-1096944	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:1096043-1096938	K562	blood:	n/a	n/a
23	BHLHE40	chr10:1094242-1095716	HepG2	liver:	n/a	n/a
24	BRCA1	chr10:1094737-1095555	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr10:1095490-1095606	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr10:1094753-1095216	HepG2	liver:	n/a	n/a
27	BRCA1	chr10:1094953-1095285	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr10:1094521-1094634	GM12878	blood:	n/a	n/a
29	BRCA1	chr10:1095799-1096042	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr10:1094837-1095280	GM12878	blood:	n/a	n/a
31	CBX3	chr10:1094808-1095670	K562	blood:	n/a	n/a
32	CBX3	chr10:1095799-1096370	K562	blood:	n/a	n/a
33	CCNT2	chr10:1096151-1096376	K562	blood:	n/a	n/a
34	CCNT2	chr10:1094229-1095869	K562	blood:	n/a	chr10:1095408-1095417 chr10:1095103-1095112
35	CEBPB	chr10:1094818-1095459	Hela-S3	cervix:	n/a	chr10:1095170-1095178
36	CEBPB	chr10:1095238-1095803	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:1094787-1095282	K562	blood:	n/a	chr10:1095170-1095178
38	CEBPB	chr10:1094821-1095142	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:1096150-1097171	K562	blood:	n/a	n/a
40	CEBPB	chr10:1094241-1094546	K562	blood:	n/a	n/a
41	CEBPD	chr10:1094686-1095594	HepG2	liver:	n/a	n/a
42	CEBPD	chr10:1096011-1096418	K562	blood:	n/a	n/a
43	CEBPD	chr10:1094604-1095517	K562	blood:	n/a	n/a
44	CEBPD	chr10:1094482-1095582	HepG2	liver:	n/a	n/a
45	CHD1	chr10:1093914-1094179	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr10:1093464-1096968	IMR90	lung:	n/a	chr10:1095411-1095421 chr10:1095080-1095087 chr10:1094729-1094739 chr10:1095408-1095418
47	CHD1	chr10:1094479-1095938	H1-hESC	embryonic stem cell:	n/a	chr10:1095411-1095421 chr10:1095080-1095087 chr10:1094729-1094739 chr10:1095408-1095418
48	CHD1	chr10:1093690-1096143	GM12878	blood:	n/a	chr10:1095411-1095421 chr10:1095080-1095087 chr10:1094729-1094739 chr10:1095408-1095418
49	CHD2	chr10:1094278-1095696	GM12878	blood:	n/a	chr10:1095411-1095421 chr10:1095080-1095087 chr10:1094729-1094739 chr10:1095408-1095418
50	CHD2	chr10:1094743-1095690	H1-hESC	embryonic stem cell:	n/a	chr10:1095411-1095421 chr10:1095080-1095087 chr10:1095408-1095418

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1095228-1095278	HL-60	blood:	n/a
2	chr10:1095069-1095119	NT2-D1	testis:	n/a
3	chr10:1095228-1095278	HL-60	blood:	n/a
4	chr10:1095069-1095119	NT2-D1	testis:	n/a
5	chr10:1095038-1095088	Hela-S3	cervix:	n/a
6	chr10:1095038-1095088	NHBE	bronchial:	n/a
7	chr10:1095554-1095604	HRE	kidney:	n/a
8	chr10:1094429-1094479	AG04449	skin:	fetal
9	chr10:1095228-1095278	AoSMC	blood vessel:	n/a
10	chr10:1095038-1095088	NB4	blood:	n/a
11	chr10:1094306-1094356	RPTEC	kidney:	n/a
12	chr10:1095446-1095496	RPTEC	kidney:	n/a
13	chr10:1095235-1095285	SK-N-MC	brain:	n/a
14	chr10:1094306-1094356	MCF10A-Er-Src	breast:	n/a
15	chr10:1095038-1095088	HepG2	liver:	n/a
16	chr10:1094306-1094356	NB4	blood:	n/a
17	chr10:1095038-1095088	BJ	skin:	n/a
18	chr10:1095554-1095604	PANC-1	pancreas:	n/a
19	chr10:1094429-1094479	HCF	heart:	n/a
20	chr10:1094976-1095026	HRE	kidney:	n/a
21	chr10:1095446-1095496	HCM	heart:	n/a
22	chr10:1095578-1095628	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:1095446-1095496	U87	brain:	n/a
24	chr10:1095446-1095496	SK-N-SH_RA	brain:	n/a
25	chr10:1095482-1095532	PFSK-1	brain:	n/a
26	chr10:1095228-1095278	GM12892	blood:	n/a
27	chr10:1095081-1095131	HRE	kidney:	n/a
28	chr10:1095235-1095285	NT2-D1	testis:	n/a
29	chr10:1094976-1095026	NT2-D1	testis:	n/a
30	chr10:1095081-1095131	AG04449	skin:	fetal
31	chr10:1095554-1095604	MCF-7	breast:	n/a
32	chr10:1095069-1095119	GM06990	blood:	n/a
33	chr10:1095578-1095628	GM12892	blood:	n/a
34	chr10:1095069-1095119	HRPEpiC	eye:	n/a
35	chr10:1094306-1094356	GM12878	blood:	n/a
36	chr10:1095554-1095604	HAEpiC	amniotic membrane:	n/a
37	chr10:1095554-1095604	H1-hESC	embryonic stem cell:	embryo
38	chr10:1095554-1095604	U87	brain:	n/a
39	chr10:1095235-1095285	MCF-7	breast:	n/a
40	chr10:1095144-1095194	SK-N-SH	brain:	n/a
41	chr10:1094976-1095026	K562	blood:	n/a
42	chr10:1095069-1095119	HUVEC	blood vessel:	n/a
43	chr10:1094976-1095026	HCM	heart:	n/a
44	chr10:1095482-1095532	GM12878	blood:	n/a
45	chr10:1095228-1095278	HUVEC	blood vessel:	n/a
46	chr10:1095482-1095532	AG04449	skin:	fetal
47	chr10:1095446-1095496	HEEpiC	esophagus:	n/a
48	chr10:1095228-1095278	MCF10A-Er-Src	breast:	n/a
49	chr10:1095578-1095628	GM12891	blood:	n/a
50	chr10:1094429-1094479	AoSMC	blood vessel:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
2	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
3	chr10:1034471..1036574-chr10:1093266..1095946,3	K562	blood:
4	chr10:1094378..1094891-chr14:74353245..74354003,2	Hela-S3	cervix:
5	chr10:1094129..1095350-chr2:122287877..122288767,3	Hela-S3	cervix:
6	chr10:1094228..1094918-chr5:56205474..56206086,2	Hela-S3	cervix:
7	chr10:1083077..1085466-chr10:1096305..1099633,3	MCF-7	breast:
8	chr1:91966057..91966769-chr10:1094298..1095218,2	Hela-S3	cervix:
9	chr10:1094316..1094876-chr5:40835238..40835957,2	Hela-S3	cervix:
10	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
11	chr10:862621..864941-chr10:1093601..1095368,2	K562	blood:
12	chr10:1094364..1094918-chr11:131779867..131780867,3	Hela-S3	cervix:
13	chr10:1094654..1095194-chr4:2936214..2937126,2	HCT-116	colon:
14	chr10:1032470..1034485-chr10:1092422..1096343,5	MCF-7	breast:
15	chr10:1095340..1097626-chr10:1118637..1120510,2	MCF-7	breast:
16	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
17	chr10:1093530..1095103-chr10:3109700..3112335,2	K562	blood:
18	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
19	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
20	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
21	chr10:1093376..1095260-chr10:1119342..1122305,3	MCF-7	breast:
22	chr10:1033990..1039615-chr10:1093691..1098446,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDI1-2	chr10:1095956-1096415	NONHSAT010896

No data

Variant related genes	Relation type
WDR37	TF binding region
IDI1	TF binding region
RNU7-163P	TF binding region
WDR37	CpG island
IDI1	CpG island
RNU7-163P	CpG island
ENSG00000107929	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000119725	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000265451	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000067057	chromatin interactions
ENSG00000229869	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000182667	chromatin interactions
ENSG00000074054	chromatin interactions

Extended variants
information (count: 209 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:209 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184649400	chr10:1091675-1091676	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs558427169	chr10:1091795-1091796	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs144000614	chr10:1091807-1091808	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs200279805	chr10:1091822-1091823	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs367766566	chr10:1091823-1091824	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs372690356	chr10:1091826-1091827	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs57575580	chr10:1091832-1091833	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs56116051	chr10:1091834-1091835	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs143135070	chr10:1091836-1091837	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs575403141	chr10:1091840-1091841	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs188280567	chr10:1091841-1091842	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs560886712	chr10:1091951-1091952	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs552536688	chr10:1091963-1091964	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs10903356	chr10:1092138-1092139	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540307453	chr10:1092143-1092144	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs560224279	chr10:1092155-1092156	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs532132942	chr10:1092181-1092182	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs552948463	chr10:1092186-1092187	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs28512382	chr10:1092195-1092196	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs531867363	chr10:1092211-1092212	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs76515647	chr10:1092220-1092221	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs568540682	chr10:1092262-1092263	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs182026490	chr10:1092275-1092276	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs548042009	chr10:1092277-1092278	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs547478806	chr10:1092296-1092297	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184970876	chr10:1092312-1092313	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs376986842	chr10:1092314-1092315	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs151222994	chr10:1092345-1092346	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs189353851	chr10:1092371-1092372	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs575511646	chr10:1092403-1092404	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs537720626	chr10:1092413-1092414	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs554775395	chr10:1092424-1092425	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs202191948	chr10:1092433-1092434	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs112173025	chr10:1092434-1092435	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs12784983	chr10:1092482-1092483	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs76676824	chr10:1092493-1092494	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs80342679	chr10:1092497-1092498	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs12761633	chr10:1092512-1092513	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs143567954	chr10:1092523-1092524	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs376115202	chr10:1092527-1092528	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs12761653	chr10:1092542-1092543	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs373192618	chr10:1092553-1092554	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs56339775	chr10:1092554-1092555	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs113447214	chr10:1092557-1092558	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs574530963	chr10:1092566-1092567	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs368171611	chr10:1092572-1092573	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs78307626	chr10:1092594-1092595	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs113791712	chr10:1092602-1092603	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs113546691	chr10:1092632-1092633	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs55736838	chr10:1092640-1092641	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1035000-1094000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:1063200-1092000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:1073400-1091800	Weak transcription	Fetal Heart	heart
4	chr10:1082600-1094000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr10:1083400-1092000	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr10:1084000-1093400	Weak transcription	Aorta	Aorta
7	chr10:1084200-1093400	Weak transcription	Thymus	Thymus
8	chr10:1087000-1092200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr10:1088000-1093400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr10:1088800-1092000	Weak transcription	Colon Smooth Muscle	Colon
11	chr10:1089200-1092800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr10:1089400-1093600	Weak transcription	Fetal Kidney	kidney
13	chr10:1089600-1092200	Weak transcription	Osteobl	bone
14	chr10:1089600-1092600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr10:1089600-1093600	Weak transcription	Placenta	Placenta
16	chr10:1089800-1091800	Weak transcription	A549	lung
17	chr10:1089800-1092000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr10:1089800-1092200	Weak transcription	Colonic Mucosa	Colon
19	chr10:1089800-1092200	Weak transcription	Ovary	ovary
20	chr10:1089800-1092200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr10:1089800-1093400	Weak transcription	Fetal Intestine Small	intestine
22	chr10:1089800-1093400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr10:1090000-1091800	Enhancers	Brain Angular Gyrus	brain
24	chr10:1090000-1092000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr10:1090000-1092200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr10:1090000-1092200	Enhancers	Adipose Nuclei	Adipose
27	chr10:1090000-1092200	Weak transcription	Esophagus	oesophagus
28	chr10:1090000-1092600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr10:1090000-1092600	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr10:1090000-1093400	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr10:1090000-1093400	Weak transcription	HSMMtube	muscle
32	chr10:1090000-1093600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:1090000-1093600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr10:1090200-1092000	Weak transcription	Fetal Intestine Large	intestine
35	chr10:1090200-1092200	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr10:1090200-1092400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr10:1090200-1092600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:1090200-1092600	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr10:1090200-1092600	Transcr. at gene 5' and 3'	Dnd41	blood
40	chr10:1090200-1092800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr10:1090200-1092800	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr10:1090400-1091800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr10:1090400-1092200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:1090400-1092200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr10:1090400-1092400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr10:1090400-1092400	Enhancers	Primary T cells from cord blood	blood
47	chr10:1090400-1092400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr10:1090400-1092400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:1090400-1092800	Enhancers	Primary B cells from peripheral blood	blood
50	chr10:1090400-1092800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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