Variant report

Variant	esv3479119
Chromosome Location	chr11:3861476-3863424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:3862890-3863079	K562	blood:	n/a	n/a
2	ATF1	chr11:3862512-3863187	K562	blood:	n/a	n/a
3	ATF2	chr11:3862870-3863245	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:3862451-3863240	GM12878	blood:	n/a	n/a
5	ATF2	chr11:3862305-3863398	GM12878	blood:	n/a	n/a
6	ATF3	chr11:3862801-3863067	A549	lung:	n/a	chr11:3862811-3862820
7	BACH1	chr11:3863088-3863148	K562	blood:	n/a	n/a
8	BATF	chr11:3862465-3863076	GM12878	blood:	n/a	n/a
9	BCL11A	chr11:3862464-3862764	GM12878	blood:	n/a	chr11:3862732-3862745 chr11:3862635-3862644
10	BCL11A	chr11:3862446-3862918	GM12878	blood:	n/a	chr11:3862732-3862745 chr11:3862635-3862644
11	BCL3	chr11:3862687-3863227	A549	lung:	n/a	chr11:3862732-3862745
12	BCL3	chr11:3862372-3862980	GM12878	blood:	n/a	chr11:3862732-3862745 chr11:3862635-3862644
13	BCLAF1	chr11:3862654-3863198	GM12878	blood:	n/a	chr11:3862732-3862745
14	BCLAF1	chr11:3862474-3863266	GM12878	blood:	n/a	chr11:3862732-3862745 chr11:3862635-3862644
15	BHLHE40	chr11:3862323-3863204	K562	blood:	n/a	n/a
16	BHLHE40	chr11:3862466-3863448	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:3861727-3862210	GM12878	blood:	n/a	chr11:3862147-3862163 chr11:3862155-3862171 chr11:3862152-3862168
18	BRCA1	chr11:3862653-3863036	GM12878	blood:	n/a	n/a
19	BRCA1	chr11:3862705-3863104	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr11:3863014-3863064	HepG2	liver:	n/a	n/a
21	CBX3	chr11:3862621-3863433	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:3862403-3863559	K562	blood:	n/a	n/a
23	CBX3	chr11:3862816-3863290	K562	blood:	n/a	n/a
24	CCNT2	chr11:3861787-3863097	K562	blood:	n/a	chr11:3862581-3862590 chr11:3862811-3862820
25	CEBPB	chr11:3862862-3863185	K562	blood:	n/a	n/a
26	CEBPB	chr11:3862787-3863507	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:3862988-3863241	K562	blood:	n/a	n/a
28	CEBPB	chr11:3862665-3863505	GM12878	blood:	n/a	n/a
29	CEBPB	chr11:3862966-3863072	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr11:3862297-3862516	HepG2	liver:	n/a	n/a
31	CEBPD	chr11:3861942-3862252	HepG2	liver:	n/a	n/a
32	CHD1	chr11:3861310-3862162	GM12878	blood:	n/a	chr11:3862080-3862090 chr11:3861719-3861726
33	CHD1	chr11:3862542-3863240	GM12878	blood:	n/a	chr11:3862849-3862859 chr11:3862812-3862822
34	CHD2	chr11:3862351-3862590	H1-hESC	embryonic stem cell:	n/a	chr11:3862512-3862519
35	CHD2	chr11:3862642-3863134	K562	blood:	n/a	chr11:3862849-3862859 chr11:3862812-3862822
36	CHD2	chr11:3862802-3863098	H1-hESC	embryonic stem cell:	n/a	chr11:3862849-3862859 chr11:3862812-3862822
37	CHD2	chr11:3861889-3863187	Hela-S3	cervix:	n/a	chr11:3862080-3862090 chr11:3862849-3862859 chr11:3862812-3862822 chr11:3862297-3862307 chr11:3862512-3862519
38	CHD2	chr11:3861995-3863171	GM12878	blood:	n/a	chr11:3862080-3862090 chr11:3862849-3862859 chr11:3862812-3862822 chr11:3862297-3862307 chr11:3862512-3862519
39	CREB1	chr11:3862512-3863092	A549	lung:	n/a	n/a
40	CREB1	chr11:3861839-3862294	A549	lung:	n/a	n/a
41	CREB1	chr11:3862054-3863202	GM12878	blood:	n/a	n/a
42	CTCF	chr11:3862900-3863050	AG04449	skin:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
43	CTCF	chr11:3862960-3863110	GM12873	blood:	n/a	chr11:3862960-3862973 chr11:3862961-3862971
44	CTCF	chr11:3862897-3863080	Kidney_OC	kidney:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
45	CTCF	chr11:3862880-3863030	HRPEpiC	eye:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
46	CTCF	chr11:3862900-3863050	HVMF	connective:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
47	CTCF	chr11:3862920-3863070	GM12871	blood:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
48	CTCF	chr11:3862900-3863050	BJ	skin:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
49	CTCF	chr11:3862920-3863070	SK-N-SH_RA	brain:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
50	CTCF	chr11:3862872-3863138	LNCaP	prostate:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3861512-3861562	MCF10A-Er-Src	breast:	n/a
2	chr11:3862931-3862981	HRPEpiC	eye:	n/a
3	chr11:3862931-3862981	HCT-116	colon:	n/a
4	chr11:3861512-3861562	MCF10A-Er-Src	breast:	n/a
5	chr11:3862931-3862981	HRPEpiC	eye:	n/a
6	chr11:3862931-3862981	HCT-116	colon:	n/a
7	chr11:3862931-3862981	AG09319	gingival:	n/a
8	chr11:3862358-3862408	HCT-116	colon:	n/a
9	chr11:3862358-3862408	BJ	skin:	n/a
10	chr11:3862089-3862139	GM12892	blood:	n/a
11	chr11:3862297-3862347	HCF	heart:	n/a
12	chr11:3862741-3862791	MCF10A-Er-Src	breast:	n/a
13	chr11:3862297-3862347	HRE	kidney:	n/a
14	chr11:3862297-3862347	ProgFib	skin:	n/a
15	chr11:3862991-3863041	NT2-D1	testis:	n/a
16	chr11:3863047-3863097	NT2-D1	testis:	n/a
17	chr11:3863056-3863106	Hela-S3	cervix:	n/a
18	chr11:3863056-3863106	U87	brain:	n/a
19	chr11:3863056-3863106	GM19239	blood:	n/a
20	chr11:3862991-3863041	NH-A	brain:	n/a
21	chr11:3862741-3862791	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:3862297-3862347	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:3862358-3862408	PrEC	prostate:	n/a
24	chr11:3862358-3862408	HRCEpiC	kidney:	n/a
25	chr11:3862302-3862352	BE2_C	brain:	n/a
26	chr11:3862358-3862408	ProgFib	skin:	n/a
27	chr11:3862089-3862139	NH-A	brain:	n/a
28	chr11:3862297-3862347	NHBE	bronchial:	n/a
29	chr11:3862741-3862791	GM12891	blood:	n/a
30	chr11:3862991-3863041	AoSMC	blood vessel:	n/a
31	chr11:3862991-3863041	HCM	heart:	n/a
32	chr11:3862931-3862981	T-47D	breast:	n/a
33	chr11:3862297-3862347	BE2_C	brain:	n/a
34	chr11:3862741-3862791	HEEpiC	esophagus:	n/a
35	chr11:3863056-3863106	HNPCEpiC	eye:	n/a
36	chr11:3862991-3863041	A549	lung:	n/a
37	chr11:3863056-3863106	HUVEC	blood vessel:	n/a
38	chr11:3862358-3862408	BE2_C	brain:	n/a
39	chr11:3862931-3862981	Hepatocyte	liver:	n/a
40	chr11:3863047-3863097	NH-A	brain:	n/a
41	chr11:3862089-3862139	HRPEpiC	eye:	n/a
42	chr11:3862297-3862347	CMK	blood:	n/a
43	chr11:3862931-3862981	GM12892	blood:	n/a
44	chr11:3863056-3863106	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:3862089-3862139	T-47D	breast:	n/a
46	chr11:3862991-3863041	RPTEC	kidney:	n/a
47	chr11:3862358-3862408	SK-N-SH	brain:	n/a
48	chr11:3862358-3862408	GM19239	blood:	n/a
49	chr11:3861512-3861562	HCM	heart:	n/a
50	chr11:3863047-3863097	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:3842483..3845464-chr11:3861552..3863945,2	MCF-7	breast:
2	chr11:3829046..3832201-chr11:3860687..3864518,3	MCF-7	breast:
3	chr11:3860029..3861574-chr11:3887601..3890496,2	K562	blood:
4	chr11:3815959..3820545-chr11:3854514..3864703,12	K562	blood:
5	chr11:3862990..3867083-chr11:3867871..3871459,5	K562	blood:
6	chr11:3861239..3864353-chr11:4095380..4099458,3	MCF-7	breast:
7	chr11:3862088..3863001-chr16:31469564..31470402,2	Hela-S3	cervix:
8	chr11:3861720..3863854-chr11:3876323..3877978,2	MCF-7	breast:
9	chr11:3817048..3820526-chr11:3859691..3864703,8	K562	blood:
10	chr11:3857497..3860664-chr11:3860718..3863734,5	MCF-7	breast:
11	chr11:3861945..3862500-chr12:52449521..52450075,2	Hela-S3	cervix:
12	chr11:3844970..3847923-chr11:3859030..3861537,2	MCF-7	breast:
13	chr11:3862483..3865232-chr11:3890007..3892959,2	K562	blood:
14	chr11:3862793..3864567-chr11:4100746..4102871,2	K562	blood:
15	chr11:3861564..3863892-chr11:4106134..4108924,2	MCF-7	breast:
16	chr11:3827764..3831807-chr11:3860648..3864124,7	K562	blood:
17	chr11:3860189..3865275-chr11:3872883..3879283,10	K562	blood:
18	chr11:3861855..3862592-chr11:61583476..61584288,2	Hela-S3	cervix:
19	chr11:3860690..3862593-chr11:4116069..4117581,2	MCF-7	breast:
20	chr11:3858623..3864245-chr11:3874959..3879217,11	K562	blood:
21	chr11:3862068..3862768-chr6:82957154..82957777,2	Hela-S3	cervix:
22	chr11:3862506..3865244-chr11:4006779..4008318,2	K562	blood:
23	chr11:3845748..3846401-chr11:3862699..3863275,2	MCF-7	breast:
24	chr11:3862693..3864773-chr11:4060192..4062998,2	MCF-7	breast:
25	chr11:3861261..3864016-chr11:3874431..3876289,3	MCF-7	breast:
26	chr11:3861999..3862694-chr12:52444941..52445740,2	Hela-S3	cervix:
27	chr11:3861567..3862305-chr16:8962537..8963094,2	Hela-S3	cervix:
28	chr11:3845241..3847374-chr11:3862493..3863741,9	K562	blood:

Variant related genes	Relation type
RHOG	TF binding region
RHOG	CpG island
ENSG00000148985	chromatin interactions
ENSG00000167323	chromatin interactions
ENSG00000263421	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000229368	chromatin interactions
ENSG00000177105	chromatin interactions
ENSG00000110713	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000167325	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000153048	chromatin interactions
ENSG00000228661	chromatin interactions
ENSG00000005700	chromatin interactions

Extended variants
information (count: 56 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:56 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568817626	chr11:3861489-3861490	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs58984815	chr11:3861585-3861586	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs138133494	chr11:3861632-3861633	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs10835184	chr11:3861650-3861651	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552314334	chr11:3861653-3861654	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs143591964	chr11:3861657-3861658	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs558685473	chr11:3861766-3861767	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs149212617	chr11:3861767-3861768	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs66864679	chr11:3861769-3861770	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs35463178	chr11:3861770-3861771	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs143334616	chr11:3861773-3861774	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs34666281	chr11:3861774-3861775	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs191982952	chr11:3861885-3861886	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs547170958	chr11:3862006-3862007	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs12278324	chr11:3862058-3862059	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11030021	chr11:3862075-3862076	Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551282365	chr11:3862088-3862089	Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs569478792	chr11:3862144-3862145	Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs539404398	chr11:3862161-3862162	Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs557509312	chr11:3862174-3862175	Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs536140052	chr11:3862286-3862287	Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs4353269	chr11:3862301-3862302	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs10835185	chr11:3862343-3862344	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555102119	chr11:3862491-3862492	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs4406820	chr11:3862533-3862534	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535527260	chr11:3862581-3862582	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs115670429	chr11:3862614-3862615	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs548721866	chr11:3862673-3862674	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs556398669	chr11:3862768-3862769	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs11030022	chr11:3862788-3862789	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs571550050	chr11:3862811-3862812	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs554186226	chr11:3862824-3862825	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs148279674	chr11:3862825-3862826	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs528556007	chr11:3862829-3862830	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs540748730	chr11:3862837-3862838	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs562240891	chr11:3862865-3862866	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs574422956	chr11:3862924-3862925	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs141343170	chr11:3862926-3862927	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs150730239	chr11:3862949-3862950	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs573180145	chr11:3862957-3862958	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs56275244	chr11:3863011-3863012	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs112700054	chr11:3863026-3863027	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs551311317	chr11:3863042-3863043	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs543289123	chr11:3863059-3863060	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs566138884	chr11:3863061-3863062	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs572486744	chr11:3863071-3863072	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs371423914	chr11:3863122-3863123	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs374648495	chr11:3863205-3863206	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs368205141	chr11:3863210-3863211	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs139054411	chr11:3863231-3863232	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3855200-3862000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
2	chr11:3857600-3861600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:3857800-3861600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
4	chr11:3857800-3861800	Flanking Active TSS	Primary hematopoietic stem cells	blood
5	chr11:3858200-3861800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:3858200-3861800	Enhancers	Fetal Heart	heart
7	chr11:3858200-3862000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:3858600-3861800	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr11:3859200-3862000	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr11:3859800-3861600	Flanking Active TSS	Fetal Thymus	thymus
11	chr11:3859800-3861600	Flanking Active TSS	Dnd41	blood
12	chr11:3859800-3861800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:3859800-3861800	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr11:3860000-3861600	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr11:3860000-3861600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr11:3860200-3861800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr11:3860400-3861600	Flanking Active TSS	Hela-S3	cervix
18	chr11:3860400-3862800	Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr11:3860400-3863000	Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chr11:3860400-3863000	Active TSS	Thymus	Thymus
21	chr11:3860400-3863000	Active TSS	GM12878-XiMat	blood
22	chr11:3860600-3861600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:3860600-3861600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:3860600-3861600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr11:3860600-3861600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:3860600-3861600	Flanking Active TSS	Brain Cingulate Gyrus	brain
27	chr11:3860600-3861600	Flanking Active TSS	Fetal Muscle Leg	muscle
28	chr11:3860600-3861800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:3860600-3861800	Flanking Active TSS	Liver	Liver
30	chr11:3860600-3861800	Flanking Active TSS	NH-A	brain
31	chr11:3860600-3862800	Active TSS	Monocytes-CD14+_RO01746	blood
32	chr11:3860600-3863000	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr11:3860600-3863000	Active TSS	Primary monocytes fromperipheralblood	blood
34	chr11:3860600-3863000	Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr11:3860600-3863000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr11:3860600-3863000	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr11:3860600-3863000	Active TSS	Left Ventricle	heart
38	chr11:3860600-3863000	Active TSS	Right Atrium	heart
39	chr11:3860600-3863000	Active TSS	HSMM	muscle
40	chr11:3860600-3863000	Active TSS	NHLF	lung
41	chr11:3860600-3863200	Active TSS	Colonic Mucosa	Colon
42	chr11:3860800-3861600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr11:3860800-3861600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:3860800-3861600	Flanking Active TSS	Brain Angular Gyrus	brain
45	chr11:3860800-3861600	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr11:3860800-3861600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr11:3860800-3861600	Flanking Active TSS	Colon Smooth Muscle	Colon
48	chr11:3860800-3861600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr11:3860800-3861600	Flanking Active TSS	Rectal Smooth Muscle	rectum
50	chr11:3860800-3861600	Flanking Active TSS	HUVEC	blood vessel

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