Variant report

Variant	nsv832162
Chromosome Location	chr11:56716658-56901528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1403)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:56894201-56894767	K562	blood:	n/a	n/a
2	ARID3A	chr11:56889946-56890139	K562	blood:	n/a	n/a
3	ARID3A	chr11:56890656-56890674	K562	blood:	n/a	n/a
4	ATF1	chr11:56749068-56749248	K562	blood:	n/a	n/a
5	ATF1	chr11:56894189-56894605	K562	blood:	n/a	n/a
6	BACH1	chr11:56804399-56804402	K562	blood:	n/a	n/a
7	BACH1	chr11:56890713-56890717	K562	blood:	n/a	n/a
8	BACH1	chr11:56896595-56896600	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr11:56839428-56839615	GM12878	blood:	n/a	n/a
10	BCL3	chr11:56839942-56840729	A549	lung:	n/a	chr11:56840270-56840279 chr11:56840269-56840278
11	BHLHE40	chr11:56894184-56894803	K562	blood:	n/a	n/a
12	BHLHE40	chr11:56892226-56892423	K562	blood:	n/a	n/a
13	BHLHE40	chr11:56898559-56898942	K562	blood:	n/a	n/a
14	BRCA1	chr11:56797626-56797633	GM12878	blood:	n/a	n/a
15	BRCA1	chr11:56898616-56898964	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr11:56894173-56894700	K562	blood:	n/a	n/a
17	CCNT2	chr11:56894158-56894974	K562	blood:	n/a	n/a
18	CEBPB	chr11:56840054-56840570	A549	lung:	n/a	n/a
19	CEBPB	chr11:56823932-56824282	HepG2	liver:	n/a	chr11:56824110-56824121
20	CEBPB	chr11:56870353-56870479	A549	lung:	n/a	n/a
21	CEBPB	chr11:56785764-56786096	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:56837400-56837764	HepG2	liver:	n/a	chr11:56837570-56837581
23	CEBPB	chr11:56773043-56773301	HepG2	liver:	n/a	chr11:56773158-56773169
24	CEBPB	chr11:56840118-56840610	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:56837408-56837744	K562	blood:	n/a	chr11:56837570-56837581
26	CEBPB	chr11:56894231-56894680	K562	blood:	n/a	n/a
27	CEBPB	chr11:56785783-56786060	A549	lung:	n/a	n/a
28	CEBPB	chr11:56894250-56894700	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:56770924-56771091	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:56837407-56837758	A549	lung:	n/a	chr11:56837570-56837581
31	CEBPB	chr11:56837382-56837880	A549	lung:	n/a	chr11:56837570-56837581
32	CEBPB	chr11:56837394-56837766	IMR90	lung:	n/a	chr11:56837570-56837581
33	CEBPB	chr11:56839959-56840804	A549	lung:	n/a	n/a
34	CEBPB	chr11:56894208-56894806	K562	blood:	n/a	n/a
35	CEBPB	chr11:56823969-56824271	A549	lung:	n/a	chr11:56824110-56824121
36	CEBPB	chr11:56894253-56894562	K562	blood:	n/a	n/a
37	CEBPB	chr11:56840076-56840734	A549	lung:	n/a	n/a
38	CEBPB	chr11:56823949-56824290	IMR90	lung:	n/a	chr11:56824110-56824121
39	CEBPB	chr11:56823955-56824296	K562	blood:	n/a	chr11:56824110-56824121
40	CEBPB	chr11:56837428-56837759	A549	lung:	n/a	chr11:56837570-56837581
41	CEBPB	chr11:56824085-56824141	H1-hESC	embryonic stem cell:	n/a	chr11:56824110-56824121
42	CEBPB	chr11:56840204-56840586	Hela-S3	cervix:	n/a	n/a
43	CEBPD	chr11:56894117-56894619	K562	blood:	n/a	n/a
44	CEBPD	chr11:56894103-56894688	K562	blood:	n/a	n/a
45	CHD2	chr11:56751942-56751995	HepG2	liver:	n/a	n/a
46	CTCF	chr11:56884160-56884310	HMF	breast:	n/a	chr11:56884245-56884263 chr11:56884248-56884261
47	CTCF	chr11:56769220-56769370	GM12864	blood:	n/a	n/a
48	CTCF	chr11:56853260-56853410	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:56884045-56884379	A549	lung:	n/a	chr11:56884245-56884263 chr11:56884248-56884261
50	CTCF	chr11:56828669-56828771	GM13977	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56891858-56891908	HL-60	blood:	n/a
2	chr11:56891858-56891908	CMK	blood:	n/a
3	chr11:56756800-56756850	Hepatocyte	liver:	n/a
4	chr11:56891858-56891908	NH-A	brain:	n/a
5	chr11:56756800-56756850	Caco-2	colon:	n/a
6	chr11:56839706-56839756	PANC-1	pancreas:	n/a
7	chr11:56756800-56756850	HCPEpiC	choroid plexus:	n/a
8	chr11:56756800-56756850	A549	lung:	n/a
9	chr11:56891858-56891908	Hela-S3	cervix:	n/a
10	chr11:56891858-56891908	Jurkat	blood:	n/a
11	chr11:56839706-56839756	SAEC	small airway:	n/a
12	chr11:56756800-56756850	HMEC	breast:	n/a
13	chr11:56839706-56839756	SK-N-SH	brain:	n/a
14	chr11:56839706-56839756	AoSMC	blood vessel:	n/a
15	chr11:56839706-56839756	Hela-S3	cervix:	n/a
16	chr11:56891858-56891908	NHDF-neo	bronchial:	n/a
17	chr11:56839706-56839756	HEK293	kidney:	embryo
18	chr11:56756800-56756850	SK-N-SH_RA	brain:	n/a
19	chr11:56756800-56756850	BJ	skin:	n/a
20	chr11:56839706-56839756	NH-A	brain:	n/a
21	chr11:56756800-56756850	CMK	blood:	n/a
22	chr11:56756800-56756850	Hela-S3	cervix:	n/a
23	chr11:56839706-56839756	NB4	blood:	n/a
24	chr11:56891858-56891908	HNPCEpiC	eye:	n/a
25	chr11:56839706-56839756	SKMC	muscle:	n/a
26	chr11:56839706-56839756	LNCaP	prostate:	n/a
27	chr11:56839706-56839756	HCF	heart:	n/a
28	chr11:56891858-56891908	GM19239	blood:	n/a
29	chr11:56839706-56839756	MCF10A-Er-Src	breast:	n/a
30	chr11:56756800-56756850	NHDF-neo	bronchial:	n/a
31	chr11:56756800-56756850	ovcar-3	ovarian:	n/a
32	chr11:56756800-56756850	Jurkat	blood:	n/a
33	chr11:56756800-56756850	SKMC	muscle:	n/a
34	chr11:56756800-56756850	SK-N-SH	brain:	n/a
35	chr11:56756800-56756850	H1-hESC	embryonic stem cell:	embryo
36	chr11:56891858-56891908	K562	blood:	n/a
37	chr11:56756800-56756850	IMR90	lung:	fetal
38	chr11:56839706-56839756	HUVEC	blood vessel:	n/a
39	chr11:56839706-56839756	BJ	skin:	n/a
40	chr11:56839706-56839756	K562	blood:	n/a
41	chr11:56756800-56756850	AoSMC	blood vessel:	n/a
42	chr11:56839706-56839756	A549	lung:	n/a
43	chr11:56839706-56839756	CMK	blood:	n/a
44	chr11:56891858-56891908	AoSMC	blood vessel:	n/a
45	chr11:56891858-56891908	A549	lung:	n/a
46	chr11:56756800-56756850	HepG2	liver:	n/a
47	chr11:56891858-56891908	IMR90	lung:	fetal
48	chr11:56756800-56756850	NB4	blood:	n/a
49	chr11:56891858-56891908	PrEC	prostate:	n/a
50	chr11:56839706-56839756	GM12878	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:56897171..56899424-chr11:57016274..57018526,19	MCF-7	breast:
2	chr11:56856802..56857496-chr12:68684950..68685726,2	MCF-7	breast:
3	chr11:56885086..56888597-chr11:56892497..56898874,6	K562	blood:
4	chr11:56891684..56895187-chr11:57015179..57019419,3	K562	blood:
5	chr11:56894422..56896558-chr11:56896581..56899282,3	K562	blood:
6	chr11:56894402..56895909-chr11:57012164..57014326,2	K562	blood:
7	chr11:56898268..56899163-chr11:57016603..57017757,8	K562	blood:
8	chr11:56894422..56896558-chr11:56896581..56899282,3	K562	blood:
9	chr11:56883857..56884825-chr11:57016233..57017822,10	MCF-7	breast:
10	chr11:56728699..56729199-chr12:122984833..122985494,2	Hela-S3	cervix:
11	chr11:56855527..56859007-chr11:56860909..56863428,3	K562	blood:
12	chr11:56885086..56888597-chr11:56892497..56898874,6	K562	blood:
13	chr11:56883739..56884861-chr11:57016166..57017852,7	K562	blood:
14	chr11:56769288..56770290-chr11:57016463..57017822,3	K562	blood:
15	chr11:56816014..56819417-chr11:56821289..56824569,3	K562	blood:
16	chr11:56767045..56768720-chr17:57919244..57922176,2	MCF-7	breast:
17	chr11:56898304..56899186-chr11:57016267..57017234,5	MCF-7	breast:
18	chr11:56888220..56889882-chr11:57010746..57012751,2	K562	blood:
19	chr11:56855527..56859007-chr11:56860909..56863428,3	K562	blood:

No data

Variant related genes	Relation type
OR5BP1P	TF binding region
OR5AK1P	TF binding region
OR5BQ1P	TF binding region
OR5AK3P	TF binding region
OR5AK2	TF binding region
OR5AO1P	TF binding region
OR5AK4P	TF binding region
OR5BP1P	CpG island
OR5AK1P	CpG island
OR5BQ1P	CpG island
OR5AK3P	CpG island
OR5AK2	CpG island
OR5AO1P	CpG island
OR5AK4P	CpG island
ENSG00000273255	chromatin interactions
ENSG00000033030	chromatin interactions

Extended variants
information (count: 3753 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3753 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568468351	chr11:56716686-56716687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535895071	chr11:56716706-56716707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557479247	chr11:56716750-56716751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1792525	chr11:56716782-56716783	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs539626138	chr11:56716824-56716825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558354274	chr11:56716827-56716828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573426804	chr11:56716830-56716831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112129592	chr11:56716857-56716858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534243579	chr11:56716897-56716898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530060755	chr11:56716946-56716947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182874350	chr11:56716962-56716963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112929237	chr11:56716972-56716973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543846100	chr11:56716992-56716993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148301413	chr11:56716997-56716998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374587828	chr11:56717026-56717027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61886697	chr11:56717059-56717060	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs140462119	chr11:56717074-56717075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145715524	chr11:56717100-56717101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138284964	chr11:56717106-56717107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549293185	chr11:56717114-56717115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569207418	chr11:56717120-56717121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116923113	chr11:56717142-56717143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370303813	chr11:56717170-56717171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142839889	chr11:56717211-56717212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186261550	chr11:56717213-56717214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567123256	chr11:56717239-56717240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150674862	chr11:56717275-56717276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138891941	chr11:56717281-56717282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551645835	chr11:56717286-56717287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76579240	chr11:56717360-56717361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534171104	chr11:56717361-56717362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373728929	chr11:56717406-56717407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189672548	chr11:56717462-56717463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537428207	chr11:56717478-56717479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149442604	chr11:56717502-56717503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1792526	chr11:56717511-56717512	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs545090386	chr11:56717515-56717516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560036917	chr11:56717521-56717522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572258059	chr11:56717528-56717529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183269159	chr11:56717529-56717530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561144137	chr11:56717557-56717558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531662653	chr11:56717652-56717653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7926761	chr11:56717661-56717662	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187554960	chr11:56717681-56717682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192194812	chr11:56717683-56717684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183545870	chr11:56717686-56717687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1792527	chr11:56717688-56717689	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs538055764	chr11:56717692-56717693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112585329	chr11:56717701-56717702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554609557	chr11:56717730-56717731	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Breast cancer	17142309	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56715800-56718600	Enhancers	Fetal Intestine Small	intestine
2	chr11:56716000-56716800	Enhancers	Stomach Mucosa	stomach
3	chr11:56716400-56717200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:56716600-56716800	Enhancers	A549	lung
5	chr11:56716600-56717000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:56717000-56718000	Enhancers	Fetal Intestine Large	intestine
7	chr11:56719800-56720200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:56720200-56720600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:56720600-56723800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:56723200-56723600	Enhancers	Adipose Nuclei	Adipose
11	chr11:56723400-56723600	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr11:56723600-56724200	Flanking Active TSS	Adipose Nuclei	Adipose
13	chr11:56723600-56724200	Active TSS	A549	lung
14	chr11:56723800-56724000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:56723800-56724200	Enhancers	Right Atrium	heart
16	chr11:56728400-56728600	Bivalent Enhancer	Aorta	Aorta
17	chr11:56735800-56736400	Enhancers	Stomach Mucosa	stomach
18	chr11:56735800-56736600	Enhancers	Esophagus	oesophagus
19	chr11:56736000-56736400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:56736000-56736600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:56736000-56736600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:56736000-56736800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:56736200-56737000	Enhancers	HMEC	breast
24	chr11:56744800-56746800	Enhancers	Stomach Mucosa	stomach
25	chr11:56748200-56748400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:56748200-56748400	Bivalent Enhancer	Liver	Liver
27	chr11:56748200-56748400	Active TSS	HMEC	breast
28	chr11:56748200-56748400	Active TSS	NHEK	skin
29	chr11:56748200-56748600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:56748200-56748600	Active TSS	Adipose Nuclei	Adipose
31	chr11:56748200-56748600	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr11:56748200-56748600	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr11:56748200-56748600	Active TSS	Right Atrium	heart
34	chr11:56748200-56748800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:56748200-56748800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:56748200-56748800	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:56748200-56748800	Active TSS	A549	lung
38	chr11:56748400-56748600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr11:56748400-56748600	Flanking Active TSS	NHEK	skin
40	chr11:56748400-56748800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:56748400-56748800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr11:56748400-56748800	Flanking Active TSS	HMEC	breast
43	chr11:56748600-56748800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:56748600-56748800	Enhancers	Adipose Nuclei	Adipose
45	chr11:56761000-56763800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:56761200-56761400	ZNF genes & repeats	Spleen	Spleen
47	chr11:56761400-56762600	Weak transcription	Spleen	Spleen
48	chr11:56762600-56763400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:56762600-56763600	ZNF genes & repeats	Adipose Nuclei	Adipose
50	chr11:56762600-56763600	ZNF genes & repeats	Spleen	Spleen

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