Variant report

Variant	nsv467792
Chromosome Location	chr11:36624187-36898373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2399)
CpG islands
(count:305)
Chromatin interactive
region (count:71)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:36724165-36724519	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:36694370-36694723	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:36768584-36768987	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:36639666-36639932	K562	blood:	n/a	n/a
5	ARID3A	chr11:36694415-36694718	K562	blood:	n/a	n/a
6	ARID3A	chr11:36634803-36634844	K562	blood:	n/a	n/a
7	ATF1	chr11:36718932-36719015	K562	blood:	n/a	n/a
8	ATF1	chr11:36692990-36693258	K562	blood:	n/a	n/a
9	ATF1	chr11:36644356-36644640	K562	blood:	n/a	n/a
10	ATF1	chr11:36768697-36768952	K562	blood:	n/a	n/a
11	ATF1	chr11:36732716-36732720	K562	blood:	n/a	n/a
12	ATF1	chr11:36654986-36654995	K562	blood:	n/a	n/a
13	ATF1	chr11:36834995-36835061	K562	blood:	n/a	n/a
14	ATF1	chr11:36679322-36679571	K562	blood:	n/a	n/a
15	ATF1	chr11:36773162-36773181	K562	blood:	n/a	n/a
16	ATF1	chr11:36639616-36640021	K562	blood:	n/a	n/a
17	ATF2	chr11:36764611-36765015	GM12878	blood:	n/a	n/a
18	ATF2	chr11:36764570-36765073	GM12878	blood:	n/a	n/a
19	ATF2	chr11:36706400-36706781	GM12878	blood:	n/a	n/a
20	ATF2	chr11:36746340-36746858	GM12878	blood:	n/a	n/a
21	ATF2	chr11:36804861-36805225	GM12878	blood:	n/a	n/a
22	BACH1	chr11:36724237-36724550	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:36784725-36785065	GM12878	blood:	n/a	chr11:36784888-36784897
24	BATF	chr11:36844446-36844671	GM12878	blood:	n/a	chr11:36844660-36844668
25	BATF	chr11:36764552-36764919	GM12878	blood:	n/a	n/a
26	BATF	chr11:36813531-36813808	GM12878	blood:	n/a	chr11:36813575-36813585
27	BATF	chr11:36724245-36724934	GM12878	blood:	n/a	n/a
28	BATF	chr11:36808891-36809216	GM12878	blood:	n/a	chr11:36809092-36809103
29	BATF	chr11:36724568-36724931	GM12878	blood:	n/a	n/a
30	BATF	chr11:36764600-36764950	GM12878	blood:	n/a	n/a
31	BATF	chr11:36784758-36784973	GM12878	blood:	n/a	chr11:36784888-36784897
32	BCL11A	chr11:36764548-36764961	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:36724469-36724860	GM12878	blood:	n/a	n/a
34	BHLHE40	chr11:36627458-36627611	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:36706487-36706688	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:36764524-36764996	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:36768556-36769024	GM12878	blood:	n/a	n/a
38	BRCA1	chr11:36724228-36724479	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr11:36768662-36768908	HepG2	liver:	n/a	n/a
40	CBX3	chr11:36766037-36766541	HCT-116	colon:	n/a	n/a
41	CBX3	chr11:36766088-36766452	K562	blood:	n/a	n/a
42	CCNT2	chr11:36631495-36631695	K562	blood:	n/a	n/a
43	CCNT2	chr11:36896217-36896380	K562	blood:	n/a	n/a
44	CEBPB	chr11:36871517-36871706	H1-hESC	embryonic stem cell:	n/a	chr11:36871633-36871644
45	CEBPB	chr11:36644359-36644647	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:36871515-36871729	HepG2	liver:	n/a	chr11:36871633-36871644
47	CEBPB	chr11:36839230-36839469	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:36724200-36724539	A549	lung:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
49	CEBPB	chr11:36809711-36809761	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:36704202-36704463	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:36723640-36723690	MCF-7	breast:	n/a
2	chr11:36807594-36807644	SK-N-SH_RA	brain:	n/a
3	chr11:36723640-36723690	HIPEpiC	eye:	n/a
4	chr11:36652206-36652256	AG04450	lung:	fetal
5	chr11:36652206-36652256	HAEpiC	amniotic membrane:	n/a
6	chr11:36723640-36723690	ovcar-3	ovarian:	n/a
7	chr11:36807594-36807644	MCF10A-Er-Src	breast:	n/a
8	chr11:36723640-36723690	SK-N-MC	brain:	n/a
9	chr11:36767011-36767061	HCPEpiC	choroid plexus:	n/a
10	chr11:36670361-36670411	ECC-1	luminal epithelium:	n/a
11	chr11:36767011-36767061	Hepatocyte	liver:	n/a
12	chr11:36670361-36670411	PFSK-1	brain:	n/a
13	chr11:36723640-36723690	GM06990	blood:	n/a
14	chr11:36807594-36807644	SKMC	muscle:	n/a
15	chr11:36767011-36767061	T-47D	breast:	n/a
16	chr11:36807594-36807644	HMEC	breast:	n/a
17	chr11:36807594-36807644	GM12878	blood:	n/a
18	chr11:36767011-36767061	SK-N-SH_RA	brain:	n/a
19	chr11:36723640-36723690	GM12891	blood:	n/a
20	chr11:36767011-36767061	AG04450	lung:	fetal
21	chr11:36767011-36767061	PANC-1	pancreas:	n/a
22	chr11:36807594-36807644	AG09319	gingival:	n/a
23	chr11:36807594-36807644	AG10803	skin:	n/a
24	chr11:36767011-36767061	PFSK-1	brain:	n/a
25	chr11:36670361-36670411	NHDF-neo	bronchial:	n/a
26	chr11:36652206-36652256	H1-hESC	embryonic stem cell:	embryo
27	chr11:36723640-36723690	NHDF-neo	bronchial:	n/a
28	chr11:36652206-36652256	MCF10A-Er-Src	breast:	n/a
29	chr11:36670361-36670411	GM12892	blood:	n/a
30	chr11:36723640-36723690	PFSK-1	brain:	n/a
31	chr11:36807594-36807644	Hela-S3	cervix:	n/a
32	chr11:36670361-36670411	HCT-116	colon:	n/a
33	chr11:36767011-36767061	NB4	blood:	n/a
34	chr11:36652206-36652256	Caco-2	colon:	n/a
35	chr11:36670361-36670411	HRE	kidney:	n/a
36	chr11:36767011-36767061	AG09309	skin:	n/a
37	chr11:36767011-36767061	ProgFib	skin:	n/a
38	chr11:36723640-36723690	GM19239	blood:	n/a
39	chr11:36807594-36807644	HEK293	kidney:	embryo
40	chr11:36670361-36670411	HAEpiC	amniotic membrane:	n/a
41	chr11:36807594-36807644	AoSMC	blood vessel:	n/a
42	chr11:36767011-36767061	GM12878	blood:	n/a
43	chr11:36807594-36807644	HNPCEpiC	eye:	n/a
44	chr11:36670361-36670411	AG09309	skin:	n/a
45	chr11:36670361-36670411	HMEC	breast:	n/a
46	chr11:36723640-36723690	PrEC	prostate:	n/a
47	chr11:36670361-36670411	GM19239	blood:	n/a
48	chr11:36767011-36767061	SK-N-MC	brain:	n/a
49	chr11:36670361-36670411	AG04449	skin:	fetal
50	chr11:36652206-36652256	NHBE	bronchial:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:36586002..36586650-chr11:36768339..36769255,5	MCF-7	breast:
2	chr11:36804091..36807084-chr11:36812047..36814004,2	MCF-7	breast:
3	chr11:36768357..36769346-chr11:36839767..36840522,2	MCF-7	breast:
4	chr11:36768357..36769346-chr11:36839767..36840522,2	MCF-7	breast:
5	chr11:36660144..36660808-chr11:36704212..36704764,2	MCF-7	breast:
6	chr11:36723937..36724844-chr11:36768321..36769390,6	K562	blood:
7	chr11:36722899..36725054-chr11:36764886..36767764,2	MCF-7	breast:
8	chr11:36805719..36807919-chr11:36809523..36812018,2	K562	blood:
9	chr11:36773100..36776427-chr11:36776879..36779629,3	K562	blood:
10	chr11:36585718..36586807-chr11:36768335..36769499,7	MCF-7	breast:
11	chr11:36588187..36588912-chr11:36768353..36769303,3	MCF-7	breast:
12	chr11:36679095..36680749-chr11:36687022..36689455,2	K562	blood:
13	chr11:36585345..36586221-chr11:36643988..36644896,2	K562	blood:
14	chr11:36778500..36779382-chr2:172367393..172368075,2	MCF-7	breast:
15	chr11:36313572..36314458-chr11:36768376..36769407,3	K562	blood:
16	chr11:36778255..36778775-chr8:120867803..120868704,2	HCT-116	colon:
17	chr11:36794916..36796666-chr11:36808832..36811328,2	K562	blood:
18	chr11:36784007..36786954-chr11:36790139..36792736,2	MCF-7	breast:
19	chr11:36536866..36537854-chr11:36768352..36769212,2	MCF-7	breast:
20	chr11:36723925..36724827-chr11:36768344..36769277,7	MCF-7	breast:
21	chr11:36772270..36775146-chr11:36778042..36780979,2	MCF-7	breast:
22	chr11:36805719..36807919-chr11:36809523..36812018,2	K562	blood:
23	chr11:36768499..36769405-chr7:29306639..29307162,2	MCF-7	breast:
24	chr11:36588028..36588693-chr11:36768352..36768969,2	MCF-7	breast:
25	chr11:36587708..36589968-chr11:36622211..36624762,2	MCF-7	breast:
26	chr11:36772768..36775100-chr11:36777744..36780242,2	K562	blood:
27	chr11:36723787..36725644-chr11:36767836..36769642,23	MCF-7	breast:
28	chr11:36724082..36725333-chr11:36765913..36767362,6	MCF-7	breast:
29	chr11:36723937..36724844-chr11:36768321..36769390,6	K562	blood:
30	chr11:36794916..36796666-chr11:36808832..36811328,2	K562	blood:
31	chr11:36585872..36586620-chr11:36765861..36766774,5	MCF-7	breast:
32	chr11:36724313..36724958-chr11:36765739..36766377,3	K562	blood:
33	chr11:36531416..36532018-chr11:36768557..36769184,2	MCF-7	breast:
34	chr11:36660144..36660808-chr11:36704212..36704764,2	MCF-7	breast:
35	chr11:36724006..36724837-chr11:36767791..36768301,2	MCF-7	breast:
36	chr11:36724082..36725333-chr11:36765913..36767362,6	MCF-7	breast:
37	chr11:36723925..36724827-chr11:36768344..36769277,7	MCF-7	breast:
38	chr11:36760152..36763496-chr11:36764810..36767505,3	K562	blood:
39	chr11:36642647..36644362-chr11:36665197..36666895,2	K562	blood:
40	chr11:36585768..36586611-chr11:36768401..36769196,4	K562	blood:
41	chr11:36844843..36847827-chr11:36858370..36860324,2	K562	blood:
42	chr11:36679095..36680749-chr11:36687022..36689455,2	K562	blood:
43	chr11:36723701..36725897-chr11:36768513..36770363,2	K562	blood:
44	chr11:36649743..36651991-chr11:36654545..36656846,2	MCF-7	breast:
45	chr11:36844843..36847827-chr11:36858370..36860324,2	K562	blood:
46	chr11:36642647..36644362-chr11:36665197..36666895,2	K562	blood:
47	chr11:36585864..36586647-chr11:36643987..36644963,5	MCF-7	breast:
48	chr11:36760152..36763496-chr11:36764810..36767505,3	K562	blood:
49	chr11:36724020..36724871-chr11:36765820..36767130,6	MCF-7	breast:
50	chr11:36710108..36712201-chr11:36728263..36730385,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf74-9	chr11:36717867-36718640	NONHSAT018837
2	lnc-C11orf74-9	chr11:36719309-36719417	NONHSAT018837

No data

Variant related genes	Relation type
RAG2	TF binding region
ENSG00000254498	TF binding region
RAG2	CpG island
ENSG00000254498	CpG island
ENSG00000136982	chromatin interactions
ENSG00000175104	chromatin interactions
ENSG00000166349	chromatin interactions

Extended variants
information (count: 7862 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:7862 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13377530	chr11:36624187-36624188	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562832413	chr11:36624269-36624270	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540120068	chr11:36624270-36624271	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531393643	chr11:36624335-36624336	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551646939	chr11:36624357-36624358	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs67981769	chr11:36624382-36624383	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs397815106	chr11:36624391-36624392	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564523268	chr11:36624403-36624404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144226692	chr11:36624440-36624441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546981086	chr11:36624463-36624464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566773617	chr11:36624522-36624523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73437905	chr11:36624574-36624575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs549404428	chr11:36624611-36624612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116421387	chr11:36624683-36624684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538004804	chr11:36624687-36624688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35583765	chr11:36624808-36624809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557941820	chr11:36624845-36624846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147759832	chr11:36624894-36624895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533666838	chr11:36625022-36625023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115777299	chr11:36625029-36625030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537284145	chr11:36625030-36625031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141241368	chr11:36625039-36625040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34563361	chr11:36625061-36625062	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12279290	chr11:36625116-36625117	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs545181999	chr11:36625137-36625138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565091385	chr11:36625194-36625195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117428479	chr11:36625195-36625196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540356287	chr11:36625237-36625238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1818003	chr11:36625246-36625247	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113495861	chr11:36625272-36625273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549362461	chr11:36625287-36625288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369835142	chr11:36625318-36625319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183968292	chr11:36625344-36625345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531900786	chr11:36625384-36625385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551533204	chr11:36625441-36625442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77042398	chr11:36625472-36625473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562737848	chr11:36625473-36625474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77918817	chr11:36625474-36625475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571489850	chr11:36625479-36625480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189287740	chr11:36625504-36625505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575172471	chr11:36625509-36625510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535771608	chr11:36625524-36625525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112601438	chr11:36625531-36625532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182172278	chr11:36625544-36625545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185563811	chr11:36625569-36625570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10501158	chr11:36625604-36625605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558918667	chr11:36625616-36625617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572260254	chr11:36625627-36625628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563608001	chr11:36625693-36625694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149079317	chr11:36625701-36625702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
WAGR syndrome	19222835	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	21829676	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36616600-36640400	Weak transcription	Esophagus	oesophagus
2	chr11:36616600-36657000	Weak transcription	Left Ventricle	heart
3	chr11:36616800-36639600	Weak transcription	Aorta	Aorta
4	chr11:36617200-36626800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:36617200-36630000	Weak transcription	HSMMtube	muscle
6	chr11:36617200-36640000	Weak transcription	Fetal Stomach	stomach
7	chr11:36617400-36632400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr11:36618000-36640400	Weak transcription	Primary T cells from cord blood	blood
9	chr11:36621000-36635400	Enhancers	Dnd41	blood
10	chr11:36622000-36625000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:36622000-36625600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:36622200-36624200	Active TSS	Thymus	Thymus
13	chr11:36622800-36625600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr11:36623000-36624800	Enhancers	Primary hematopoietic stem cells	blood
15	chr11:36623600-36624400	Active TSS	Fetal Thymus	thymus
16	chr11:36624000-36624200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr11:36624200-36624400	Flanking Active TSS	Thymus	Thymus
18	chr11:36624200-36627200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr11:36624400-36627800	Enhancers	Thymus	Thymus
20	chr11:36624400-36628000	Enhancers	Fetal Thymus	thymus
21	chr11:36624800-36626800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr11:36625000-36626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:36625600-36626200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:36625600-36626600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:36626200-36628200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr11:36626400-36627000	Enhancers	GM12878-XiMat	blood
27	chr11:36626600-36627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:36626800-36627400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:36626800-36627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:36626800-36627800	Enhancers	Primary hematopoietic stem cells	blood
31	chr11:36626800-36641000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:36627000-36627400	Flanking Active TSS	GM12878-XiMat	blood
33	chr11:36627200-36627400	Enhancers	Psoas Muscle	Psoas
34	chr11:36627200-36627400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr11:36627200-36627600	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr11:36627200-36627800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:36627400-36628000	Enhancers	GM12878-XiMat	blood
38	chr11:36627400-36630200	Weak transcription	Psoas Muscle	Psoas
39	chr11:36627400-36639800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr11:36627600-36631000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr11:36627600-36631800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:36627800-36629400	Weak transcription	Thymus	Thymus
43	chr11:36627800-36639000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr11:36628000-36629400	Weak transcription	Fetal Thymus	thymus
45	chr11:36628200-36630800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr11:36628400-36637600	Weak transcription	Colon Smooth Muscle	Colon
47	chr11:36628600-36628800	Active TSS	Fetal Kidney	kidney
48	chr11:36628800-36640200	Weak transcription	Fetal Kidney	kidney
49	chr11:36629400-36631200	Enhancers	Fetal Thymus	thymus
50	chr11:36629400-36631800	Enhancers	Thymus	Thymus

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