Variant report

Variant	nsv976446
Chromosome Location	chr11:3626480-3648596
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	chr11:3630802-3631209	K562	blood:	n/a	n/a
2	ARID3A	chr11:3626269-3626631	K562	blood:	n/a	n/a
3	BHLHE40	chr11:3635535-3636206	K562	blood:	n/a	n/a
4	BHLHE40	chr11:3635894-3636214	GM12878	blood:	n/a	n/a
5	CBX3	chr11:3647544-3647861	K562	blood:	n/a	n/a
6	CTCF	chr11:3635328-3635403	Lung_OC	lung:	n/a	n/a
7	CTCF	chr11:3630980-3631130	AG04450	lung:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
8	CTCF	chr11:3631000-3631150	HFF	foreskin:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
9	CTCF	chr11:3631000-3631150	HEEpiC	esophagus:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
10	CTCF	chr11:3631400-3631550	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr11:3630993-3631204	MCF-7	breast:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
12	CTCF	chr11:3631040-3631190	GM12872	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
13	CTCF	chr11:3630980-3631130	HCT-116	colon:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
14	CTCF	chr11:3647640-3647790	GM12874	blood:	n/a	n/a
15	CTCF	chr11:3630880-3631030	A549	lung:	n/a	n/a
16	CTCF	chr11:3631000-3631150	AG09319	gingival:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
17	CTCF	chr11:3647702-3647767	MCF-7	breast:	n/a	n/a
18	CTCF	chr11:3631000-3631150	HL-60	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
19	CTCF	chr11:3630978-3631211	LNCaP	prostate:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
20	CTCF	chr11:3631340-3631490	GM12874	blood:	n/a	n/a
21	CTCF	chr11:3647680-3647830	K562	blood:	n/a	n/a
22	CTCF	chr11:3630180-3630330	SAEC	small airway:	n/a	n/a
23	CTCF	chr11:3647680-3647830	HEK293	kidney:	n/a	n/a
24	CTCF	chr11:3630964-3631234	GM12878	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
25	CTCF	chr11:3647628-3647840	GM19238	blood:	n/a	n/a
26	CTCF	chr11:3647575-3648034	K562	blood:	n/a	n/a
27	CTCF	chr11:3630586-3631483	A549	lung:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
28	CTCF	chr11:3631020-3631170	HUVEC	blood vessel:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
29	CTCF	chr11:3647682-3647832	GM13977	blood:	n/a	n/a
30	CTCF	chr11:3631040-3631190	GM12864	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
31	CTCF	chr11:3631008-3631224	GM19240	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
32	CTCF	chr11:3631060-3631210	WI-38	lung:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
33	CTCF	chr11:3631360-3631510	GM06990	blood:	n/a	n/a
34	CTCF	chr11:3630960-3631110	HFF-Myc	foreskin:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
35	CTCF	chr11:3631000-3631150	AoAF	blood vessel:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
36	CTCF	chr11:3630941-3631219	Medullo	brain:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
37	CTCF	chr11:3630920-3631070	HAc	cerebellar:	n/a	n/a
38	CTCF	chr11:3631014-3631218	A549	lung:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
39	CTCF	chr11:3631520-3631670	GM12872	blood:	n/a	n/a
40	CTCF	chr11:3631020-3631170	GM12866	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
41	CTCF	chr11:3631040-3631190	SAEC	small airway:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
42	CTCF	chr11:3631020-3631170	GM12865	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
43	CTCF	chr11:3647614-3647840	K562	blood:	n/a	n/a
44	CTCF	chr11:3628238-3628286	GM10248	blood:	n/a	n/a
45	CTCF	chr11:3647651-3647825	GM12892	blood:	n/a	n/a
46	CTCF	chr11:3647640-3647790	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr11:3630872-3631198	K562	blood:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092
48	CTCF	chr11:3631320-3631470	Caco-2	colon:	n/a	n/a
49	CTCF	chr11:3631383-3631474	GM10248	blood:	n/a	n/a
50	CTCF	chr11:3630949-3631220	HUVEC	blood vessel:	n/a	chr11:3631078-3631094 chr11:3631077-3631095 chr11:3631067-3631074 chr11:3631072-3631093 chr11:3631083-3631092

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3647086-3647136	AoSMC	blood vessel:	n/a
2	chr11:3647086-3647136	AoSMC	blood vessel:	n/a
3	chr11:3637658-3637708	AG04450	lung:	fetal
4	chr11:3647419-3647469	PANC-1	pancreas:	n/a
5	chr11:3647419-3647469	NT2-D1	testis:	n/a
6	chr11:3647695-3647745	PrEC	prostate:	n/a
7	chr11:3647654-3647704	T-47D	breast:	n/a
8	chr11:3648013-3648063	HNPCEpiC	eye:	n/a
9	chr11:3638352-3638402	BJ	skin:	n/a
10	chr11:3638352-3638402	MCF10A-Er-Src	breast:	n/a
11	chr11:3638448-3638498	LNCaP	prostate:	n/a
12	chr11:3648013-3648063	PFSK-1	brain:	n/a
13	chr11:3637658-3637708	RPTEC	kidney:	n/a
14	chr11:3647365-3647415	T-47D	breast:	n/a
15	chr11:3647365-3647415	GM06990	blood:	n/a
16	chr11:3647419-3647469	HCPEpiC	choroid plexus:	n/a
17	chr11:3638458-3638508	GM12878	blood:	n/a
18	chr11:3647654-3647704	HL-60	blood:	n/a
19	chr11:3638458-3638508	SK-N-MC	brain:	n/a
20	chr11:3638352-3638402	Hela-S3	cervix:	n/a
21	chr11:3648013-3648063	K562	blood:	n/a
22	chr11:3648013-3648063	SK-N-SH	brain:	n/a
23	chr11:3638458-3638508	HCF	heart:	n/a
24	chr11:3647654-3647704	GM12891	blood:	n/a
25	chr11:3647365-3647415	GM12892	blood:	n/a
26	chr11:3647654-3647704	GM12878	blood:	n/a
27	chr11:3638458-3638508	RPTEC	kidney:	n/a
28	chr11:3638352-3638402	ProgFib	skin:	n/a
29	chr11:3638448-3638498	HUVEC	blood vessel:	n/a
30	chr11:3647419-3647469	HCT-116	colon:	n/a
31	chr11:3647086-3647136	HMEC	breast:	n/a
32	chr11:3647654-3647704	SK-N-SH_RA	brain:	n/a
33	chr11:3648013-3648063	SK-N-MC	brain:	n/a
34	chr11:3638458-3638508	HCM	heart:	n/a
35	chr11:3647695-3647745	ProgFib	skin:	n/a
36	chr11:3647695-3647745	SKMC	muscle:	n/a
37	chr11:3637427-3637477	SAEC	small airway:	n/a
38	chr11:3637427-3637477	HRPEpiC	eye:	n/a
39	chr11:3647365-3647415	HCF	heart:	n/a
40	chr11:3647419-3647469	PFSK-1	brain:	n/a
41	chr11:3637427-3637477	IMR90	lung:	fetal
42	chr11:3637658-3637708	NB4	blood:	n/a
43	chr11:3648013-3648063	A549	lung:	n/a
44	chr11:3638448-3638498	GM12878	blood:	n/a
45	chr11:3648013-3648063	Jurkat	blood:	n/a
46	chr11:3637658-3637708	HRCEpiC	kidney:	n/a
47	chr11:3647695-3647745	Jurkat	blood:	n/a
48	chr11:3638448-3638498	A549	lung:	n/a
49	chr11:3647695-3647745	Hela-S3	cervix:	n/a
50	chr11:3637658-3637708	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
2	chr11:3635682..3637406-chr11:3642517..3644691,2	K562	blood:
3	chr11:3635375..3637756-chr11:3638069..3640906,2	K562	blood:
4	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
5	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:
6	chr11:3635682..3637406-chr11:3642517..3644691,2	K562	blood:
7	chr11:3624727..3627376-chr11:3629301..3631751,2	K562	blood:
8	chr11:3498062..3499877-chr11:3626508..3628362,2	MCF-7	breast:
9	chr11:3640981..3643163-chr11:3645928..3648472,2	K562	blood:
10	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:

Variant related genes	Relation type
OR7E117P	TF binding region
TRPC2	TF binding region
OR7E117P	CpG island
TRPC2	CpG island
ENSG00000182048	chromatin interactions

Extended variants
information (count: 964 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574886017	chr11:3626487-3626488	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs369988096	chr11:3626501-3626502	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs188753942	chr11:3626613-3626614	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547381865	chr11:3626619-3626620	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs150288851	chr11:3626655-3626656	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs560952016	chr11:3626662-3626663	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs137947902	chr11:3626669-3626670	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs142408403	chr11:3626679-3626680	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs146367555	chr11:3626690-3626691	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs375097240	chr11:3626693-3626694	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532742282	chr11:3626810-3626811	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs138446748	chr11:3626814-3626815	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs114127317	chr11:3626815-3626816	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs181178650	chr11:3626833-3626834	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs142932628	chr11:3626869-3626870	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112941454	chr11:3626930-3626931	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs12418667	chr11:3626947-3626948	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186214875	chr11:3626952-3626953	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs115215350	chr11:3626966-3626967	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376104314	chr11:3627050-3627051	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553137798	chr11:3627052-3627053	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs386749910	chr11:3627079-3627080	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189024635	chr11:3627086-3627087	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs370968820	chr11:3627088-3627089	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs554918361	chr11:3627090-3627091	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576377215	chr11:3627113-3627114	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs543643773	chr11:3627115-3627116	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs7951724	chr11:3627164-3627165	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11028440	chr11:3627183-3627184	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs541119351	chr11:3627185-3627186	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76041742	chr11:3627198-3627199	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs181488611	chr11:3627215-3627216	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78868641	chr11:3627221-3627222	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs60899201	chr11:3627242-3627243	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs531064111	chr11:3627343-3627344	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201538217	chr11:3627363-3627364	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552365731	chr11:3627366-3627367	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570705370	chr11:3627386-3627387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528605187	chr11:3627401-3627402	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs11603475	chr11:3627420-3627421	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs539241677	chr11:3627431-3627432	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs61066729	chr11:3627469-3627470	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191853361	chr11:3627492-3627493	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs568424745	chr11:3627514-3627515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs60991845	chr11:3627536-3627537	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs58044045	chr11:3627537-3627538	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569802638	chr11:3627550-3627551	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs57650571	chr11:3627572-3627573	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs59714051	chr11:3627593-3627594	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs184998494	chr11:3627599-3627600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3606400-3635800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:3625400-3627400	Enhancers	Fetal Intestine Large	intestine
3	chr11:3625600-3627000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:3625600-3627000	Weak transcription	Right Atrium	heart
5	chr11:3626000-3629000	Enhancers	Placenta	Placenta
6	chr11:3626200-3627000	Active TSS	Duodenum Mucosa	Duodenum
7	chr11:3626400-3627200	Enhancers	K562	blood
8	chr11:3626400-3627400	Enhancers	Fetal Intestine Small	intestine
9	chr11:3627000-3627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:3627000-3627200	Enhancers	Right Atrium	heart
11	chr11:3627000-3627400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr11:3627400-3627800	Weak transcription	Fetal Intestine Large	intestine
13	chr11:3627400-3627800	Weak transcription	Fetal Intestine Small	intestine
14	chr11:3627800-3628200	Enhancers	Fetal Intestine Large	intestine
15	chr11:3627800-3628200	Enhancers	Fetal Intestine Small	intestine
16	chr11:3628800-3629000	Enhancers	NHDF-Ad	bronchial
17	chr11:3628800-3629400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:3632000-3632800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:3634000-3634200	Enhancers	Lung	lung
20	chr11:3634200-3635800	Weak transcription	Lung	lung
21	chr11:3634800-3635200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr11:3634800-3635400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:3634800-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:3634800-3636800	Enhancers	Primary hematopoietic stem cells	blood
25	chr11:3635000-3635200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr11:3635000-3635200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:3635000-3635400	Enhancers	Colon Smooth Muscle	Colon
30	chr11:3635000-3635400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr11:3635000-3636200	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr11:3635000-3636400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:3635000-3636400	Enhancers	Right Ventricle	heart
34	chr11:3635000-3639200	Enhancers	Fetal Muscle Leg	muscle
35	chr11:3635200-3635600	Enhancers	Primary T cells from cord blood	blood
36	chr11:3635200-3635600	Enhancers	Adipose Nuclei	Adipose
37	chr11:3635200-3636000	Enhancers	Right Atrium	heart
38	chr11:3635200-3636000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr11:3635200-3636000	Enhancers	Thymus	Thymus
40	chr11:3635200-3636200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr11:3635200-3636200	Enhancers	Left Ventricle	heart
42	chr11:3635200-3636400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr11:3635200-3636400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:3635200-3636400	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:3635200-3636400	Enhancers	Primary B cells from peripheral blood	blood
46	chr11:3635200-3636400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr11:3635200-3636400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:3635200-3636400	Enhancers	Fetal Thymus	thymus
49	chr11:3635200-3636400	Enhancers	K562	blood
50	chr11:3635200-3636400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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