Variant report

Variant	nsv897077
Chromosome Location	chr11:24091682-24308924
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	BRCA1	chr11:24134525-24134539	GM12878	blood:	n/a	n/a
2	CEBPB	chr11:24154112-24154390	ECC-1	luminal epithelium:	n/a	chr11:24154249-24154260
3	CEBPB	chr11:24156453-24156796	Hela-S3	cervix:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
4	CEBPB	chr11:24249542-24249602	HepG2	liver:	n/a	chr11:24249555-24249566
5	CEBPB	chr11:24220767-24221066	HepG2	liver:	n/a	chr11:24220898-24220909
6	CEBPB	chr11:24299076-24299370	IMR90	lung:	n/a	chr11:24299202-24299213
7	CEBPB	chr11:24258173-24258539	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:24286432-24286807	IMR90	lung:	n/a	chr11:24286614-24286625
9	CEBPB	chr11:24286441-24286782	HepG2	liver:	n/a	chr11:24286614-24286625
10	CEBPB	chr11:24154088-24154396	IMR90	lung:	n/a	chr11:24154249-24154260
11	CEBPB	chr11:24177885-24178052	A549	lung:	n/a	n/a
12	CEBPB	chr11:24154086-24154414	HepG2	liver:	n/a	chr11:24154249-24154260
13	CEBPB	chr11:24154137-24154400	Hela-S3	cervix:	n/a	chr11:24154249-24154260
14	CEBPB	chr11:24286490-24286757	A549	lung:	n/a	chr11:24286614-24286625
15	CEBPB	chr11:24254614-24254909	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:24258158-24258513	A549	lung:	n/a	n/a
17	CEBPB	chr11:24156525-24156739	ECC-1	luminal epithelium:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
18	CEBPB	chr11:24156454-24156816	HepG2	liver:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
19	CEBPB	chr11:24188751-24188939	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:24286473-24286778	K562	blood:	n/a	chr11:24286614-24286625
21	CEBPB	chr11:24299149-24299349	HepG2	liver:	n/a	chr11:24299202-24299213
22	CEBPB	chr11:24156398-24156785	A549	lung:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
23	CEBPB	chr11:24156440-24156810	IMR90	lung:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
24	CEBPB	chr11:24220865-24220955	K562	blood:	n/a	chr11:24220898-24220909
25	CEBPB	chr11:24220776-24221089	IMR90	lung:	n/a	chr11:24220898-24220909
26	CEBPB	chr11:24286473-24286785	Hela-S3	cervix:	n/a	chr11:24286614-24286625
27	CEBPB	chr11:24156460-24156780	H1-hESC	embryonic stem cell:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
28	CEBPB	chr11:24281388-24281661	A549	lung:	n/a	chr11:24281546-24281557 chr11:24281546-24281559
29	CEBPB	chr11:24286523-24286771	H1-hESC	embryonic stem cell:	n/a	chr11:24286614-24286625
30	CEBPB	chr11:24260498-24260902	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:24254599-24254935	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:24308545-24308811	K562	blood:	n/a	chr11:24308663-24308676 chr11:24308665-24308676 chr11:24308663-24308674 chr11:24308663-24308676
33	CEBPB	chr11:24154130-24154389	MCF-7	breast:	n/a	chr11:24154249-24154260
34	CEBPB	chr11:24156457-24156830	MCF-7	breast:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
35	CEBPB	chr11:24308521-24308827	HepG2	liver:	n/a	chr11:24308663-24308676 chr11:24308665-24308676 chr11:24308663-24308674 chr11:24308663-24308676
36	CEBPB	chr11:24273857-24274081	H1-hESC	embryonic stem cell:	n/a	chr11:24273965-24273976 chr11:24273965-24273978
37	CEBPB	chr11:24156436-24156809	MCF-7	breast:	n/a	chr11:24156615-24156626 chr11:24156632-24156643
38	CEBPB	chr11:24254596-24254839	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:24154151-24154362	H1-hESC	embryonic stem cell:	n/a	chr11:24154249-24154260
40	CEBPB	chr11:24154067-24154422	ECC-1	luminal epithelium:	n/a	chr11:24154249-24154260
41	CHD1	chr11:24226116-24226285	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr11:24256880-24257030	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr11:24177380-24177530	GM12878	blood:	n/a	n/a
44	CTCF	chr11:24256820-24256970	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr11:24256770-24257013	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:24256800-24256950	RPTEC	kidney:	n/a	n/a
47	CTCF	chr11:24256840-24256990	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr11:24256820-24256970	AG04449	skin:	n/a	n/a
49	CTCF	chr11:24177480-24177630	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr11:24212300-24212450	GM12870	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24260751-24260801	U87	brain:	n/a
2	chr11:24275293-24275343	Hepatocyte	liver:	n/a
3	chr11:24101781-24101831	SK-N-SH	brain:	n/a
4	chr11:24260751-24260801	HMEC	breast:	n/a
5	chr11:24275293-24275343	RPTEC	kidney:	n/a
6	chr11:24260751-24260801	AG10803	skin:	n/a
7	chr11:24101781-24101831	SKMC	muscle:	n/a
8	chr11:24101781-24101831	A549	lung:	n/a
9	chr11:24275293-24275343	MCF-7	breast:	n/a
10	chr11:24275293-24275343	HCPEpiC	choroid plexus:	n/a
11	chr11:24260751-24260801	AG04450	lung:	fetal
12	chr11:24101781-24101831	HCT-116	colon:	n/a
13	chr11:24260751-24260801	Hela-S3	cervix:	n/a
14	chr11:24260751-24260801	MCF-7	breast:	n/a
15	chr11:24275293-24275343	Hela-S3	cervix:	n/a
16	chr11:24101781-24101831	GM12891	blood:	n/a
17	chr11:24101781-24101831	HRE	kidney:	n/a
18	chr11:24260751-24260801	NH-A	brain:	n/a
19	chr11:24275293-24275343	HRE	kidney:	n/a
20	chr11:24101781-24101831	U87	brain:	n/a
21	chr11:24260751-24260801	SAEC	small airway:	n/a
22	chr11:24260751-24260801	AoSMC	blood vessel:	n/a
23	chr11:24275293-24275343	AG09319	gingival:	n/a
24	chr11:24101781-24101831	H1-hESC	embryonic stem cell:	embryo
25	chr11:24260751-24260801	GM06990	blood:	n/a
26	chr11:24260751-24260801	AG04449	skin:	fetal
27	chr11:24260751-24260801	HCT-116	colon:	n/a
28	chr11:24275293-24275343	GM06990	blood:	n/a
29	chr11:24260751-24260801	HCF	heart:	n/a
30	chr11:24101781-24101831	HUVEC	blood vessel:	n/a
31	chr11:24101781-24101831	NB4	blood:	n/a
32	chr11:24275293-24275343	LNCaP	prostate:	n/a
33	chr11:24260751-24260801	LNCaP	prostate:	n/a
34	chr11:24275293-24275343	H1-hESC	embryonic stem cell:	embryo
35	chr11:24260751-24260801	HAEpiC	amniotic membrane:	n/a
36	chr11:24101781-24101831	ECC-1	luminal epithelium:	n/a
37	chr11:24101781-24101831	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:24101781-24101831	GM06990	blood:	n/a
39	chr11:24101781-24101831	PFSK-1	brain:	n/a
40	chr11:24101781-24101831	AG04450	lung:	fetal
41	chr11:24275293-24275343	AoSMC	blood vessel:	n/a
42	chr11:24101781-24101831	AG09319	gingival:	n/a
43	chr11:24260751-24260801	SK-N-SH_RA	brain:	n/a
44	chr11:24260751-24260801	PANC-1	pancreas:	n/a
45	chr11:24260751-24260801	H1-hESC	embryonic stem cell:	embryo
46	chr11:24260751-24260801	IMR90	lung:	fetal
47	chr11:24101781-24101831	PrEC	prostate:	n/a
48	chr11:24101781-24101831	Hela-S3	cervix:	n/a
49	chr11:24275293-24275343	HIPEpiC	eye:	n/a
50	chr11:24275293-24275343	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:24160485..24163375-chr11:24163857..24165450,2	MCF-7	breast:
2	chr11:23561735..23562349-chr11:24176838..24178049,3	MCF-7	breast:
3	chr11:24221833..24223887-chr11:24233684..24236438,2	K562	blood:
4	chr11:24202163..24204133-chr11:24208051..24210770,2	MCF-7	breast:
5	chr11:24202163..24204133-chr11:24208051..24210770,2	MCF-7	breast:
6	chr11:23993865..23994676-chr11:24177072..24177577,2	MCF-7	breast:
7	chr11:24160485..24163375-chr11:24163857..24165450,2	MCF-7	breast:
8	chr11:24221833..24223887-chr11:24233684..24236438,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-3	chr11:24283627-24283764	ENSG00000254594
2	lnc-RP11-17A1.2.1-3	chr11:24281464-24281559	ENSG00000254594
3	lnc-RP11-17A1.2.1-3	chr11:24281464-24281559	ENSG00000254594
4	lnc-RP11-17A1.2.1-3	chr11:24279738-24279857	ENSG00000254594
5	lnc-RP11-17A1.2.1-3	chr11:24280945-24281108	ENSG00000254594
6	lnc-RP11-17A1.2.1-3	chr11:24270419-24270475	ENSG00000254594
7	lnc-RP11-17A1.2.1-3	chr11:24280982-24281108	ENSG00000254594
8	lnc-RP11-17A1.2.1-3	chr11:24257023-24257051	ENSG00000254594
9	lnc-RP11-17A1.2.1-3	chr11:24283627-24283751	ENSG00000254594

Variant related genes	Relation type
ENSG00000254594	TF binding region
ENSG00000254594	CpG island

Extended variants
information (count: 3065 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3065 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10834273	chr11:24091682-24091683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549107175	chr11:24091699-24091700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1915070	chr11:24091750-24091751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs202177779	chr11:24091767-24091768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534388349	chr11:24091777-24091778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547701329	chr11:24091803-24091804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571109724	chr11:24091848-24091849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186986395	chr11:24091880-24091881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556474498	chr11:24091897-24091898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576038312	chr11:24091902-24091903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139725502	chr11:24091903-24091904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs16912064	chr11:24091943-24091944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192377251	chr11:24091949-24091950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540813975	chr11:24091981-24091982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550156130	chr11:24091986-24091987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61876477	chr11:24092012-24092013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114024282	chr11:24092013-24092014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543351997	chr11:24092025-24092026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563254122	chr11:24092027-24092028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199639581	chr11:24092061-24092062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397849035	chr11:24092062-24092063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200001047	chr11:24092063-24092064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377719805	chr11:24092090-24092091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528885265	chr11:24092104-24092105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370155810	chr11:24092163-24092164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547450264	chr11:24092228-24092229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72881183	chr11:24092267-24092268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139938677	chr11:24092315-24092316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149774803	chr11:24092342-24092343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570960321	chr11:24092348-24092349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556657968	chr11:24092352-24092353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147887311	chr11:24092368-24092369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550198494	chr11:24092400-24092401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2176793	chr11:24092402-24092403	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs535437528	chr11:24092490-24092491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371173160	chr11:24092506-24092507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111548112	chr11:24092527-24092528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183292290	chr11:24092534-24092535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188586832	chr11:24092547-24092548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552100228	chr11:24092551-24092552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534832280	chr11:24092592-24092593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557884730	chr11:24092596-24092597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181830833	chr11:24098818-24098819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111655199	chr11:24098828-24098829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552653583	chr11:24098851-24098852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577583147	chr11:24098883-24098884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7118340	chr11:24098885-24098886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113409873	chr11:24098919-24098920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544462601	chr11:24098928-24098929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538300846	chr11:24098940-24098941	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24086400-24091800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr11:24086400-24091800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:24086800-24091800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr11:24087400-24092000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:24091600-24092000	Weak transcription	Fetal Brain Male	brain
6	chr11:24091600-24092200	Enhancers	Brain Germinal Matrix	brain
7	chr11:24091800-24092200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr11:24091800-24092400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:24091800-24092400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:24091800-24092600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr11:24091800-24092600	Enhancers	Fetal Brain Female	brain
12	chr11:24092000-24092400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr11:24092000-24092400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:24092000-24092600	Enhancers	Fetal Brain Male	brain
15	chr11:24098800-24099200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:24099200-24100200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:24099400-24099800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:24099600-24100000	Enhancers	Fetal Lung	lung
19	chr11:24099800-24100200	Enhancers	Stomach Mucosa	stomach
20	chr11:24100200-24101000	Enhancers	Ovary	ovary
21	chr11:24100200-24101400	Enhancers	NHLF	lung
22	chr11:24100200-24101600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:24101600-24104400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:24104000-24104800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr11:24104400-24105200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:24110600-24111400	Enhancers	Fetal Lung	lung
27	chr11:24111400-24114400	Weak transcription	Fetal Lung	lung
28	chr11:24114400-24114600	Enhancers	Fetal Lung	lung
29	chr11:24114400-24114800	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr11:24114400-24114800	Enhancers	HUVEC	blood vessel
31	chr11:24114600-24115000	Flanking Active TSS	Fetal Lung	lung
32	chr11:24114600-24115200	Enhancers	Dnd41	blood
33	chr11:24114600-24115400	Enhancers	Brain Germinal Matrix	brain
34	chr11:24114800-24115000	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr11:24115000-24116000	Enhancers	Fetal Lung	lung
36	chr11:24115200-24116000	Enhancers	Fetal Brain Female	brain
37	chr11:24122200-24123200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:24128600-24128800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:24136400-24140400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:24143800-24144200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:24159000-24159800	Enhancers	HUVEC	blood vessel
42	chr11:24163600-24164600	Enhancers	Dnd41	blood
43	chr11:24163600-24164800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:24171600-24172000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:24171800-24172000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:24171800-24172000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:24176400-24177000	Enhancers	Pancreas	Pancrea
48	chr11:24176600-24177200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:24176600-24177400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:24177400-24178000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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