Variant report

Variant	nsv897064
Chromosome Location	chr11:23767292-23859991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:23808741-23808892	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:23791141-23791164	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:23844303-23844514	HepG2	liver:	n/a	chr11:23844394-23844405
4	CEBPB	chr11:23794359-23794613	HepG2	liver:	n/a	chr11:23794482-23794495 chr11:23794482-23794493
5	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
6	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
7	CEBPB	chr11:23820772-23821109	A549	lung:	n/a	n/a
8	CEBPB	chr11:23777366-23777662	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
10	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
11	CEBPB	chr11:23844250-23844479	IMR90	lung:	n/a	chr11:23844394-23844405
12	CEBPB	chr11:23808790-23808947	HepG2	liver:	n/a	chr11:23808906-23808917
13	CEBPB	chr11:23777380-23777595	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
15	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117
16	CHD1	chr11:23789645-23789701	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr11:23855960-23856110	AG04449	skin:	n/a	n/a
18	CTCF	chr11:23855880-23856030	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr11:23855940-23856090	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr11:23855960-23856110	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr11:23855920-23856070	HCM	heart:	n/a	n/a
22	CTCF	chr11:23855940-23856090	AG04449	skin:	n/a	n/a
23	CTCF	chr11:23855960-23856110	AG10803	skin:	n/a	n/a
24	CTCF	chr11:23855940-23856090	NHEK	skin:	n/a	n/a
25	CTCF	chr11:23769747-23769786	Lung_OC	lung:	n/a	n/a
26	CTCF	chr11:23855960-23856110	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr11:23855960-23856110	AG09319	gingival:	n/a	n/a
28	CTCF	chr11:23855986-23856130	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:23855926-23856203	IMR90	lung:	n/a	n/a
30	CTCF	chr11:23855880-23856030	HAc	cerebellar:	n/a	n/a
31	CTCF	chr11:23855860-23856010	HVMF	connective:	n/a	n/a
32	CTCF	chr11:23855960-23856110	HRE	kidney:	n/a	n/a
33	CTCF	chr11:23855940-23856090	BJ	skin:	n/a	n/a
34	CTCF	chr11:23855996-23856120	Medullo	brain:	n/a	n/a
35	CTCF	chr11:23855980-23856130	NHLF	lung:	n/a	n/a
36	CTCF	chr11:23849360-23849510	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:23849268-23849376	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr11:23855940-23856090	HMF	breast:	n/a	n/a
39	CTCF	chr11:23855956-23856145	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr11:23855980-23856130	HMEC	breast:	n/a	n/a
41	CTCF	chr11:23855967-23856138	Fibrobl	skin:	n/a	n/a
42	CTCF	chr11:23855952-23856153	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:23855940-23856090	SAEC	small airway:	n/a	n/a
44	CTCF	chr11:23855989-23856128	Gliobla	brain:	n/a	n/a
45	CTCF	chr11:23827236-23827314	ProgFib	skin:	n/a	n/a
46	CTCF	chr11:23856139-23856154	Fibrobl	skin:	n/a	n/a
47	CTCF	chr11:23855920-23856070	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr11:23855860-23856010	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr11:23856000-23856150	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr11:23855936-23856164	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23811425-23811475	AG04450	lung:	fetal
2	chr11:23811425-23811475	T-47D	breast:	n/a
3	chr11:23811425-23811475	BE2_C	brain:	n/a
4	chr11:23811425-23811475	HepG2	liver:	n/a
5	chr11:23811425-23811475	HCF	heart:	n/a
6	chr11:23811425-23811475	AG04449	skin:	fetal
7	chr11:23811425-23811475	SK-N-MC	brain:	n/a
8	chr11:23811425-23811475	HCPEpiC	choroid plexus:	n/a
9	chr11:23811425-23811475	HCT-116	colon:	n/a
10	chr11:23811425-23811475	GM12892	blood:	n/a
11	chr11:23811425-23811475	MCF-7	breast:	n/a
12	chr11:23811425-23811475	IMR90	lung:	fetal
13	chr11:23811425-23811475	CMK	blood:	n/a
14	chr11:23811425-23811475	NHDF-neo	bronchial:	n/a
15	chr11:23811425-23811475	HUVEC	blood vessel:	n/a
16	chr11:23811425-23811475	LNCaP	prostate:	n/a
17	chr11:23811425-23811475	Hela-S3	cervix:	n/a
18	chr11:23811425-23811475	HMEC	breast:	n/a
19	chr11:23811425-23811475	NHBE	bronchial:	n/a
20	chr11:23811425-23811475	GM06990	blood:	n/a
21	chr11:23811425-23811475	HRE	kidney:	n/a
22	chr11:23811425-23811475	Caco-2	colon:	n/a
23	chr11:23811425-23811475	NB4	blood:	n/a
24	chr11:23811425-23811475	MCF10A-Er-Src	breast:	n/a
25	chr11:23811425-23811475	Hepatocyte	liver:	n/a
26	chr11:23811425-23811475	HNPCEpiC	eye:	n/a
27	chr11:23811425-23811475	AG09319	gingival:	n/a
28	chr11:23811425-23811475	ProgFib	skin:	n/a
29	chr11:23811425-23811475	ovcar-3	ovarian:	n/a
30	chr11:23811425-23811475	SAEC	small airway:	n/a
31	chr11:23811425-23811475	GM12891	blood:	n/a
32	chr11:23811425-23811475	HRCEpiC	kidney:	n/a
33	chr11:23811425-23811475	U87	brain:	n/a
34	chr11:23811425-23811475	Jurkat	blood:	n/a
35	chr11:23811425-23811475	HEEpiC	esophagus:	n/a
36	chr11:23811425-23811475	AG10803	skin:	n/a
37	chr11:23811425-23811475	PrEC	prostate:	n/a
38	chr11:23811425-23811475	NT2-D1	testis:	n/a
39	chr11:23811425-23811475	SKMC	muscle:	n/a
40	chr11:23811425-23811475	K562	blood:	n/a
41	chr11:23811425-23811475	GM12878	blood:	n/a
42	chr11:23811425-23811475	H1-hESC	embryonic stem cell:	embryo
43	chr11:23811425-23811475	BJ	skin:	n/a
44	chr11:23811425-23811475	HAEpiC	amniotic membrane:	n/a
45	chr11:23811425-23811475	HIPEpiC	eye:	n/a
46	chr11:23811425-23811475	AoSMC	blood vessel:	n/a
47	chr11:23811425-23811475	HEK293	kidney:	embryo
48	chr11:23811425-23811475	HCM	heart:	n/a
49	chr11:23811425-23811475	ECC-1	luminal epithelium:	n/a
50	chr11:23811425-23811475	NH-A	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:23798376..23799116-chr5:32449587..32450235,2	MCF-7	breast:
2	chr11:23766902..23769192-chr6:80655556..80658439,2	MCF-7	breast:
3	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
4	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-2	chr11:23782899-23783176	XLOC_009394
2	lnc-RP11-17A1.2.1-2	chr11:23782876-23783176	ENSG00000254861
3	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
4	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
5	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430
6	lnc-RP11-17A1.2.1-2	chr11:23789323-23789362	XLOC_009394
7	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395
8	lnc-RP11-17A1.2.1-2	chr11:23802334-23802418	ENSG00000254861
9	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
10	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
11	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193

No data

Variant related genes	Relation type
ENSG00000254861	TF binding region
ENSG00000254861	CpG island
ENSG00000118402	chromatin interactions

Extended variants
information (count: 2565 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4472941	chr11:23767292-23767293	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs193190894	chr11:23767367-23767368	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184616508	chr11:23767429-23767430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188355540	chr11:23767456-23767457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563906449	chr11:23767592-23767593	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568591475	chr11:23767593-23767594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192151230	chr11:23767600-23767601	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542328469	chr11:23767603-23767604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559056195	chr11:23767616-23767617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577281884	chr11:23767636-23767637	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528171109	chr11:23767637-23767638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183652462	chr11:23767646-23767647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs4533035	chr11:23767708-23767709	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs115317700	chr11:23767726-23767727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188336568	chr11:23767763-23767764	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552545211	chr11:23767776-23767777	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529787722	chr11:23767787-23767788	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181808801	chr11:23767844-23767845	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546797082	chr11:23767868-23767869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184818445	chr11:23767873-23767874	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535110602	chr11:23767900-23767901	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188800117	chr11:23767906-23767907	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114372211	chr11:23767909-23767910	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562961242	chr11:23767917-23767918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552892968	chr11:23768013-23768014	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182058868	chr11:23768024-23768025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79644130	chr11:23768028-23768029	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145126148	chr11:23768032-23768033	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186156410	chr11:23768044-23768045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs80045623	chr11:23768049-23768050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191446972	chr11:23768069-23768070	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs9651581	chr11:23768143-23768144	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564917210	chr11:23768218-23768219	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7121714	chr11:23768229-23768230	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138233509	chr11:23768250-23768251	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530394799	chr11:23768268-23768269	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148344568	chr11:23768339-23768340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546459634	chr11:23768370-23768371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561197462	chr11:23768388-23768389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570924798	chr11:23768459-23768460	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181424594	chr11:23768464-23768465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141587871	chr11:23768519-23768520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528596963	chr11:23768556-23768557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185311229	chr11:23768578-23768579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs551553455	chr11:23768598-23768599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530826944	chr11:23768659-23768660	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571630232	chr11:23768662-23768663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531938842	chr11:23768680-23768681	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537083177	chr11:23768720-23768721	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557301074	chr11:23768803-23768804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	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
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23769000-23769400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr11:23769400-23771200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:23771200-23771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:23771200-23772000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:23771200-23772400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:23771400-23771800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:23771600-23772400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:23771600-23776600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:23772000-23776600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:23772200-23772600	Enhancers	Gastric	stomach
11	chr11:23772400-23782400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:23775400-23775800	Enhancers	Colon Smooth Muscle	Colon
13	chr11:23776600-23777400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:23776600-23777800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:23777000-23778200	Enhancers	Adipose Nuclei	Adipose
16	chr11:23778600-23779000	Enhancers	Fetal Intestine Large	intestine
17	chr11:23780800-23781400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:23781200-23781400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr11:23781400-23785400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:23781400-23787200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr11:23782000-23783200	Enhancers	Fetal Lung	lung
22	chr11:23782400-23783200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:23785400-23789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:23786200-23786400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr11:23787000-23788200	Enhancers	Placenta Amnion	Placenta Amnion
26	chr11:23787200-23788000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:23787200-23788000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:23787200-23788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:23789200-23792000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:23790200-23791200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr11:23790400-23791800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:23792600-23794200	Enhancers	Fetal Stomach	stomach
33	chr11:23792800-23794200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:23794200-23795200	Weak transcription	Fetal Stomach	stomach
35	chr11:23795200-23795400	Enhancers	Fetal Stomach	stomach
36	chr11:23798600-23799200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr11:23799200-23803200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:23799600-23802400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr11:23800400-23802000	Enhancers	NH-A	brain
40	chr11:23800600-23802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:23800800-23801200	Enhancers	HSMM	muscle
42	chr11:23801200-23811000	Weak transcription	HSMM	muscle
43	chr11:23803200-23803600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:23803600-23804600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:23804600-23806800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:23805200-23806400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr11:23805800-23806200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:23806200-23811200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:23806400-23806600	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr11:23806400-23807000	Enhancers	HepG2	liver

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