Variant report

Variant	nsv898035
Chromosome Location	chr11:84420132-84497615
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	chr11:84425391-84425616	HepG2	liver:	n/a	n/a
2	ATF2	chr11:84425281-84425625	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:84453284-84453645	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr11:84465652-84465923	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:84423471-84423495	GM12878	blood:	n/a	n/a
6	CBX3	chr11:84425239-84425761	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:84425346-84425608	K562	blood:	n/a	n/a
8	CEBPB	chr11:84441166-84441336	A549	lung:	n/a	n/a
9	CEBPB	chr11:84455324-84455488	K562	blood:	n/a	chr11:84455338-84455349
10	CEBPB	chr11:84441215-84441415	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:84455217-84455511	A549	lung:	n/a	chr11:84455338-84455349
12	CEBPB	chr11:84455235-84455534	IMR90	lung:	n/a	chr11:84455338-84455349
13	CEBPB	chr11:84483215-84483418	HepG2	liver:	n/a	n/a
14	CTBP2	chr11:84430898-84432454	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr11:84491880-84492030	NHLF	lung:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
16	CTCF	chr11:84491860-84492010	HMEC	breast:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
17	CTCF	chr11:84425420-84425570	HepG2	liver:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
18	CTCF	chr11:84491839-84492024	GM13977	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
19	CTCF	chr11:84425440-84425590	GM06990	blood:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
20	CTCF	chr11:84491860-84492010	Caco-2	colon:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
21	CTCF	chr11:84425460-84425610	HAc	cerebellar:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
22	CTCF	chr11:84425424-84425614	H1-hESC	embryonic stem cell:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
23	CTCF	chr11:84491860-84492010	GM12872	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
24	CTCF	chr11:84433740-84433890	RPTEC	kidney:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
25	CTCF	chr11:84491884-84491980	K562	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
26	CTCF	chr11:84425420-84425570	HRE	kidney:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
27	CTCF	chr11:84491880-84492030	NHDF-neo	bronchial:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
28	CTCF	chr11:84491900-84492050	GM12865	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
29	CTCF	chr11:84491815-84492123	H1-hESC	embryonic stem cell:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
30	CTCF	chr11:84433799-84433859	Pancreas_OC	pancreas:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
31	CTCF	chr11:84425405-84425640	NHEK	skin:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
32	CTCF	chr11:84491860-84492010	GM12865	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
33	CTCF	chr11:84425780-84425930	Caco-2	colon:	n/a	n/a
34	CTCF	chr11:84425431-84425586	K562	blood:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
35	CTCF	chr11:84491820-84491970	SAEC	small airway:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
36	CTCF	chr11:84433700-84433850	SK-N-SH_RA	brain:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
37	CTCF	chr11:84425380-84425530	A549	lung:	n/a	n/a
38	CTCF	chr11:84433772-84433888	Hela-S3	cervix:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
39	CTCF	chr11:84491820-84491970	GM12873	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
40	CTCF	chr11:84433702-84434001	H1-hESC	embryonic stem cell:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
41	CTCF	chr11:84433740-84433890	GM12878	blood:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
42	CTCF	chr11:84491860-84492010	WERI-Rb-1	eye:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
43	CTCF	chr11:84451500-84451650	HepG2	liver:	n/a	n/a
44	CTCF	chr11:84425440-84425590	HEK293	kidney:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
45	CTCF	chr11:84425430-84425756	K562	blood:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
46	CTCF	chr11:84491840-84491990	HEEpiC	esophagus:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
47	CTCF	chr11:84491880-84492030	GM12865	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
48	CTCF	chr11:84491860-84492010	AoAF	blood vessel:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
49	CTCF	chr11:84491822-84492081	MCF-7	breast:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
50	CTCF	chr11:84491753-84492211	HCT-116	colon:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:84431918-84431968	HEK293	kidney:	embryo
2	chr11:84431918-84431968	HEK293	kidney:	embryo
3	chr11:84432312-84432362	Hepatocyte	liver:	n/a
4	chr11:84431970-84432020	ProgFib	skin:	n/a
5	chr11:84432312-84432362	NHDF-neo	bronchial:	n/a
6	chr11:84431850-84431900	NHBE	bronchial:	n/a
7	chr11:84431918-84431968	GM06990	blood:	n/a
8	chr11:84432312-84432362	NB4	blood:	n/a
9	chr11:84431850-84431900	U87	brain:	n/a
10	chr11:84432312-84432362	AG04449	skin:	fetal
11	chr11:84431918-84431968	GM12878	blood:	n/a
12	chr11:84431970-84432020	AG10803	skin:	n/a
13	chr11:84431535-84431585	HCF	heart:	n/a
14	chr11:84432312-84432362	SKMC	muscle:	n/a
15	chr11:84431850-84431900	SK-N-MC	brain:	n/a
16	chr11:84431970-84432020	AG04450	lung:	fetal
17	chr11:84431918-84431968	BE2_C	brain:	n/a
18	chr11:84431535-84431585	AoSMC	blood vessel:	n/a
19	chr11:84431535-84431585	HRCEpiC	kidney:	n/a
20	chr11:84431535-84431585	HEEpiC	esophagus:	n/a
21	chr11:84431850-84431900	SK-N-SH_RA	brain:	n/a
22	chr11:84432312-84432362	HL-60	blood:	n/a
23	chr11:84431850-84431900	HL-60	blood:	n/a
24	chr11:84431918-84431968	Hela-S3	cervix:	n/a
25	chr11:84431535-84431585	HL-60	blood:	n/a
26	chr11:84431535-84431585	NT2-D1	testis:	n/a
27	chr11:84431535-84431585	PrEC	prostate:	n/a
28	chr11:84431918-84431968	HRCEpiC	kidney:	n/a
29	chr11:84431970-84432020	AG04449	skin:	fetal
30	chr11:84432312-84432362	NHBE	bronchial:	n/a
31	chr11:84431850-84431900	GM19239	blood:	n/a
32	chr11:84431918-84431968	T-47D	breast:	n/a
33	chr11:84432312-84432362	PANC-1	pancreas:	n/a
34	chr11:84431535-84431585	MCF-7	breast:	n/a
35	chr11:84431850-84431900	NB4	blood:	n/a
36	chr11:84431850-84431900	ECC-1	luminal epithelium:	n/a
37	chr11:84432312-84432362	HEEpiC	esophagus:	n/a
38	chr11:84431918-84431968	GM12892	blood:	n/a
39	chr11:84432312-84432362	AG09309	skin:	n/a
40	chr11:84431535-84431585	HNPCEpiC	eye:	n/a
41	chr11:84431850-84431900	NT2-D1	testis:	n/a
42	chr11:84431850-84431900	ovcar-3	ovarian:	n/a
43	chr11:84432312-84432362	SAEC	small airway:	n/a
44	chr11:84431918-84431968	PANC-1	pancreas:	n/a
45	chr11:84431535-84431585	HUVEC	blood vessel:	n/a
46	chr11:84431535-84431585	NHDF-neo	bronchial:	n/a
47	chr11:84431850-84431900	NH-A	brain:	n/a
48	chr11:84432312-84432362	GM06990	blood:	n/a
49	chr11:84431918-84431968	Jurkat	blood:	n/a
50	chr11:84431970-84432020	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:84492333..84495051-chr11:84901283..84903076,2	MCF-7	breast:
2	chr11:84470491..84472543-chr11:84477634..84479392,2	MCF-7	breast:
3	chr11:84268829..84269798-chr11:84425022..84425965,7	MCF-7	breast:
4	chr11:84353205..84353720-chr11:84425398..84425994,2	MCF-7	breast:
5	chr11:84433336..84434202-chr11:85301668..85302606,6	MCF-7	breast:
6	chr11:84353266..84354226-chr11:84425005..84426301,12	MCF-7	breast:
7	chr11:84268928..84269579-chr11:84425061..84426012,3	MCF-7	breast:
8	chr11:84382646..84384164-chr11:84421223..84423854,2	MCF-7	breast:
9	chr11:84101140..84101859-chr11:84425077..84425854,3	MCF-7	breast:
10	chr11:84491046..84493285-chr11:84497010..84499873,2	MCF-7	breast:
11	chr11:84269079..84271717-chr11:84447544..84450102,2	MCF-7	breast:
12	chr11:84491944..84492445-chr11:85301546..85302502,2	MCF-7	breast:
13	chr11:84269617..84270472-chr11:84425387..84425965,2	MCF-7	breast:
14	chr11:84491891..84492728-chr11:84673979..84674886,2	MCF-7	breast:
15	chr11:84269134..84270255-chr11:84430304..84431248,5	MCF-7	breast:
16	chr11:84268874..84269428-chr11:84491493..84492369,2	MCF-7	breast:
17	chr11:84491046..84493285-chr11:84497010..84499873,2	MCF-7	breast:
18	chr11:84435745..84436679-chr11:85301971..85302607,2	MCF-7	breast:
19	chr11:84494003..84496842-chr11:85300062..85301679,2	MCF-7	breast:
20	chr11:84470491..84472543-chr11:84477634..84479392,2	MCF-7	breast:
21	chr11:84415255..84417235-chr11:84419666..84422634,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM126B-2	chr11:84431869-84431924	ENSG00000254787.1
2	lnc-TMEM126B-2	chr11:84473154-84473211	ENSG00000254787.1
3	lnc-TMEM126B-2	chr11:84474333-84474398	ENSG00000254787.1

Variant related genes	Relation type
ENSG00000254787	TF binding region
ENSG00000254787	CpG island

Extended variants
information (count: 2115 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2115 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs472587	chr11:84420132-84420133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538356292	chr11:84420148-84420149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192934183	chr11:84420152-84420153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544379966	chr11:84420178-84420179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562932159	chr11:84420187-84420188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56289023	chr11:84420209-84420210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs149661058	chr11:84420215-84420216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554107436	chr11:84420236-84420237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572377095	chr11:84420247-84420248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542604312	chr11:84420255-84420256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560955302	chr11:84420270-84420271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576028787	chr11:84420275-84420276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58826664	chr11:84420285-84420286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184171026	chr11:84420362-84420363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140802551	chr11:84420363-84420364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144650858	chr11:84420436-84420437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58566021	chr11:84420478-84420479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560373752	chr11:84420501-84420502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370791497	chr11:84420560-84420561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527990445	chr11:84420609-84420610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544965364	chr11:84420619-84420620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549077526	chr11:84420705-84420706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567626636	chr11:84420712-84420713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189364941	chr11:84420732-84420733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550240407	chr11:84420748-84420749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571818659	chr11:84420762-84420763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560433148	chr11:84420796-84420797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538793782	chr11:84420804-84420805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554021978	chr11:84420810-84420811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565945906	chr11:84420817-84420818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536571208	chr11:84420821-84420822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554596500	chr11:84420864-84420865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575976904	chr11:84420906-84420907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148479766	chr11:84420940-84420941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181008712	chr11:84420945-84420946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576538770	chr11:84420952-84420953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545160669	chr11:84420958-84420959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560334700	chr11:84420976-84420977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74804506	chr11:84421030-84421031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527930907	chr11:84421062-84421063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74584123	chr11:84421065-84421066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549173389	chr11:84421068-84421069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567748836	chr11:84421118-84421119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184877510	chr11:84421119-84421120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189636220	chr11:84421147-84421148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181438048	chr11:84421262-84421263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186118284	chr11:84421284-84421285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116914684	chr11:84421296-84421297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533955905	chr11:84421340-84421341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565862205	chr11:84421375-84421376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Cancer	20164920	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84414000-84424200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:84424200-84424600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr11:84424600-84425400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:84425200-84425400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr11:84425200-84425400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:84425200-84425800	Active TSS	Dnd41	blood
7	chr11:84425400-84426600	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr11:84425600-84426000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:84425600-84426000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:84425800-84426200	Flanking Active TSS	Dnd41	blood
11	chr11:84426600-84429000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr11:84429000-84429400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr11:84429400-84429800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr11:84429600-84431000	Active TSS	Brain Cingulate Gyrus	brain
15	chr11:84429800-84430800	Active TSS	Brain Anterior Caudate	brain
16	chr11:84429800-84432200	Active TSS	Brain Hippocampus Middle	brain
17	chr11:84429800-84432600	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr11:84430000-84430600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr11:84430000-84430800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr11:84430000-84432600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:84430200-84430600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr11:84430200-84430600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:84430200-84431000	Enhancers	Primary T cells from cord blood	blood
24	chr11:84430400-84430800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr11:84430400-84430800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr11:84430400-84430800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
27	chr11:84430400-84430800	Enhancers	Thymus	Thymus
28	chr11:84430400-84431000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:84430400-84431000	Active TSS	Fetal Brain Female	brain
30	chr11:84430400-84432600	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr11:84430600-84430800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr11:84430600-84430800	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr11:84430600-84430800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr11:84430600-84430800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr11:84430600-84430800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:84430600-84430800	Enhancers	Brain Germinal Matrix	brain
37	chr11:84430600-84430800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:84430600-84431000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:84430600-84431000	Enhancers	Fetal Brain Male	brain
40	chr11:84430800-84431000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr11:84430800-84431000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:84430800-84431000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr11:84430800-84431000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr11:84430800-84431000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:84430800-84431000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr11:84430800-84431000	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:84430800-84431000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
48	chr11:84430800-84431000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr11:84430800-84431000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr11:84430800-84431000	Active TSS	Brain Angular Gyrus	brain

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