Variant report

Variant	nsv1058391
Chromosome Location	chr22:34324887-34418020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:62)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 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	chr22:34397243-34397472	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:34392790-34393312	HepG2	liver:	n/a	n/a
3	BACH1	chr22:34381644-34381723	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr22:34382949-34383312	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr22:34360783-34360867	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr22:34388413-34388764	HepG2	liver:	n/a	n/a
7	CEBPB	chr22:34367447-34367858	MCF-7	breast:	n/a	chr22:34367627-34367638
8	CEBPB	chr22:34388430-34388714	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr22:34397170-34397548	HepG2	liver:	n/a	chr22:34397353-34397364 chr22:34397354-34397365 chr22:34397483-34397500 chr22:34397353-34397366
10	CEBPB	chr22:34388421-34388741	IMR90	lung:	n/a	n/a
11	CEBPB	chr22:34397264-34397428	HepG2	liver:	n/a	chr22:34397353-34397364 chr22:34397354-34397365 chr22:34397353-34397366
12	CEBPB	chr22:34375229-34375392	HepG2	liver:	n/a	chr22:34375314-34375325
13	CEBPB	chr22:34379465-34379694	A549	lung:	n/a	chr22:34379566-34379577
14	CEBPB	chr22:34354237-34354513	IMR90	lung:	n/a	chr22:34354383-34354394
15	CEBPB	chr22:34379410-34379656	IMR90	lung:	n/a	chr22:34379566-34379577
16	CEBPB	chr22:34388438-34388654	K562	blood:	n/a	n/a
17	CEBPB	chr22:34388466-34388743	A549	lung:	n/a	n/a
18	CEBPB	chr22:34404199-34404478	HepG2	liver:	n/a	chr22:34404318-34404335 chr22:34404320-34404331 chr22:34404319-34404332 chr22:34404319-34404330
19	CEBPB	chr22:34379414-34379735	HepG2	liver:	n/a	chr22:34379566-34379577
20	CEBPB	chr22:34354267-34354518	HepG2	liver:	n/a	chr22:34354383-34354394
21	CEBPB	chr22:34367480-34367798	A549	lung:	n/a	chr22:34367627-34367638
22	CEBPB	chr22:34367446-34367838	H1-hESC	embryonic stem cell:	n/a	chr22:34367627-34367638
23	CEBPB	chr22:34367451-34367820	HepG2	liver:	n/a	chr22:34367627-34367638
24	CEBPB	chr22:34367451-34367815	IMR90	lung:	n/a	chr22:34367627-34367638
25	CEBPB	chr22:34367535-34367798	Hela-S3	cervix:	n/a	chr22:34367627-34367638
26	CEBPB	chr22:34379461-34379593	H1-hESC	embryonic stem cell:	n/a	chr22:34379566-34379577
27	CEBPB	chr22:34390782-34390933	HepG2	liver:	n/a	chr22:34390823-34390834
28	CTCF	chr22:34415540-34415690	A549	lung:	n/a	n/a
29	CTCF	chr22:34415603-34415702	Lung_OC	lung:	n/a	n/a
30	CTCF	chr22:34415543-34415740	MCF-7	breast:	n/a	n/a
31	CTCF	chr22:34415560-34415710	HepG2	liver:	n/a	n/a
32	CTCF	chr22:34325013-34325032	Lung_OC	lung:	n/a	n/a
33	CTCF	chr22:34415512-34415660	HepG2	liver:	n/a	n/a
34	CTCF	chr22:34415560-34415710	NHEK	skin:	n/a	n/a
35	CTCF	chr22:34378220-34378370	GM12868	blood:	n/a	n/a
36	CTCF	chr22:34385707-34385749	Fibrobl	skin:	n/a	n/a
37	CTCF	chr22:34349700-34349850	GM12864	blood:	n/a	n/a
38	CTCF	chr22:34330475-34330559	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr22:34415618-34415660	LNCaP	prostate:	n/a	n/a
40	CTCF	chr22:34401894-34401961	K562	blood:	n/a	n/a
41	CTCF	chr22:34415616-34415674	LNCaP	prostate:	n/a	n/a
42	CTCF	chr22:34415597-34415664	GM12892	blood:	n/a	n/a
43	CTCF	chr22:34415562-34415676	MCF-7	breast:	n/a	n/a
44	CTCF	chr22:34374010-34374080	GM12878	blood:	n/a	n/a
45	CTCF	chr22:34415494-34415788	MCF-7	breast:	n/a	n/a
46	CTCF	chr22:34415576-34415697	NHEK	skin:	n/a	n/a
47	CTCF	chr22:34415559-34415710	MCF-7	breast:	n/a	n/a
48	CTCF	chr22:34358208-34358254	GM10248	blood:	n/a	n/a
49	CTCF	chr22:34415536-34415753	MCF-7	breast:	n/a	n/a
50	CTCF	chr22:34415560-34415710	GM12864	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34383032-34383082	LNCaP	prostate:	n/a
2	chr22:34383032-34383082	LNCaP	prostate:	n/a
3	chr22:34383032-34383082	HRE	kidney:	n/a
4	chr22:34383032-34383082	PFSK-1	brain:	n/a
5	chr22:34383032-34383082	AG09319	gingival:	n/a
6	chr22:34383032-34383082	HEK293	kidney:	embryo
7	chr22:34383032-34383082	SK-N-SH_RA	brain:	n/a
8	chr22:34383032-34383082	AoSMC	blood vessel:	n/a
9	chr22:34383032-34383082	Jurkat	blood:	n/a
10	chr22:34383032-34383082	U87	brain:	n/a
11	chr22:34383032-34383082	Hepatocyte	liver:	n/a
12	chr22:34383032-34383082	BE2_C	brain:	n/a
13	chr22:34383032-34383082	HPAEpiC	pulmonary alveolar:	n/a
14	chr22:34383032-34383082	ProgFib	skin:	n/a
15	chr22:34383032-34383082	GM12892	blood:	n/a
16	chr22:34383032-34383082	HL-60	blood:	n/a
17	chr22:34383032-34383082	HAEpiC	amniotic membrane:	n/a
18	chr22:34383032-34383082	K562	blood:	n/a
19	chr22:34383032-34383082	SAEC	small airway:	n/a
20	chr22:34383032-34383082	RPTEC	kidney:	n/a
21	chr22:34383032-34383082	HRPEpiC	eye:	n/a
22	chr22:34383032-34383082	AG10803	skin:	n/a
23	chr22:34383032-34383082	GM19239	blood:	n/a
24	chr22:34383032-34383082	GM12878	blood:	n/a
25	chr22:34383032-34383082	NT2-D1	testis:	n/a
26	chr22:34383032-34383082	HCM	heart:	n/a
27	chr22:34383032-34383082	NHBE	bronchial:	n/a
28	chr22:34383032-34383082	BJ	skin:	n/a
29	chr22:34383032-34383082	HCT-116	colon:	n/a
30	chr22:34383032-34383082	SKMC	muscle:	n/a
31	chr22:34383032-34383082	PrEC	prostate:	n/a
32	chr22:34383032-34383082	PANC-1	pancreas:	n/a
33	chr22:34383032-34383082	IMR90	lung:	fetal
34	chr22:34383032-34383082	H1-hESC	embryonic stem cell:	embryo
35	chr22:34383032-34383082	HUVEC	blood vessel:	n/a
36	chr22:34383032-34383082	HEEpiC	esophagus:	n/a
37	chr22:34383032-34383082	HRCEpiC	kidney:	n/a
38	chr22:34383032-34383082	T-47D	breast:	n/a
39	chr22:34383032-34383082	HNPCEpiC	eye:	n/a
40	chr22:34383032-34383082	HCPEpiC	choroid plexus:	n/a
41	chr22:34383032-34383082	AG04449	skin:	fetal
42	chr22:34383032-34383082	A549	lung:	n/a
43	chr22:34383032-34383082	GM12891	blood:	n/a
44	chr22:34383032-34383082	GM06990	blood:	n/a
45	chr22:34383032-34383082	Hela-S3	cervix:	n/a
46	chr22:34383032-34383082	NH-A	brain:	n/a
47	chr22:34383032-34383082	HepG2	liver:	n/a
48	chr22:34383032-34383082	HIPEpiC	eye:	n/a
49	chr22:34383032-34383082	Caco-2	colon:	n/a
50	chr22:34383032-34383082	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:34409232..34410755-chr22:34412827..34414607,2	MCF-7	breast:
2	chr22:34317156..34319746-chr22:34329020..34331193,2	MCF-7	breast:
3	chr22:34315414..34317058-chr22:34327574..34329120,2	MCF-7	breast:
4	chr22:34319321..34320710-chr22:34415195..34416586,9	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISX-3	chr22:34413462-34413516	ENSG00000236052

No data

Variant related genes	Relation type
ENSG00000236052	TF binding region
ENSG00000236052	CpG island
ENSG00000273082	chromatin interactions
ENSG00000236052	chromatin interactions
ENSG00000133424	chromatin interactions

Extended variants
information (count: 2211 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2211 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145251023	chr22:34326213-34326214	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs12484434	chr22:34326316-34326317	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs544443403	chr22:34326322-34326323	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs191650460	chr22:34326367-34326368	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs7284214	chr22:34326399-34326400	Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1962597	chr22:34326430-34326431	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs560457356	chr22:34326441-34326442	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs371391000	chr22:34326519-34326520	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs9621807	chr22:34326529-34326530	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542219843	chr22:34326535-34326536	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs562203402	chr22:34326562-34326563	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs531453142	chr22:34326569-34326570	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs551259675	chr22:34326652-34326653	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs571403329	chr22:34326685-34326686	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs1962596	chr22:34326711-34326712	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184420381	chr22:34326748-34326749	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs114410608	chr22:34326779-34326780	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs376543965	chr22:34326790-34326791	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs535805082	chr22:34326805-34326806	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs142428020	chr22:34326807-34326808	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs569223261	chr22:34326815-34326816	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs538313383	chr22:34326821-34326822	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs73408428	chr22:34326854-34326855	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs578118062	chr22:34326875-34326876	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs540474935	chr22:34326913-34326914	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs554000131	chr22:34326919-34326920	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs574003886	chr22:34326943-34326944	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs1962595	chr22:34326955-34326956	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs187768607	chr22:34326976-34326977	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs5999145	chr22:34326987-34326988	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs374602307	chr22:34327000-34327001	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs5754759	chr22:34327007-34327008	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527436069	chr22:34327011-34327012	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs113059755	chr22:34327086-34327087	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs567529524	chr22:34327130-34327131	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs530037537	chr22:34327131-34327132	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs550125964	chr22:34327149-34327150	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs193128258	chr22:34327177-34327178	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs138523391	chr22:34327200-34327201	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs185627206	chr22:34327211-34327212	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs528417357	chr22:34327223-34327224	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs140723972	chr22:34327251-34327252	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs5994812	chr22:34327276-34327277	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534086879	chr22:34327313-34327314	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs189099302	chr22:34327384-34327385	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs5999146	chr22:34327395-34327396	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs5999147	chr22:34327399-34327400	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181550274	chr22:34327420-34327421	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs150077501	chr22:34327432-34327433	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs184173067	chr22:34327441-34327442	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34326200-34326400	Flanking Bivalent TSS/Enh	Fetal Heart	heart
2	chr22:34326400-34327800	Bivalent Enhancer	Fetal Heart	heart
3	chr22:34328600-34329400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr22:34328800-34329200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr22:34329000-34329400	Enhancers	NHEK	skin
6	chr22:34329200-34329600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr22:34334600-34335000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr22:34334600-34335200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr22:34339000-34340200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr22:34348400-34349600	Enhancers	Brain Anterior Caudate	brain
11	chr22:34348400-34349600	Enhancers	Brain Hippocampus Middle	brain
12	chr22:34348400-34349600	Enhancers	Brain Substantia Nigra	brain
13	chr22:34348600-34349800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr22:34348800-34349000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr22:34348800-34349200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr22:34349000-34349400	Bivalent Enhancer	Brain Germinal Matrix	brain
17	chr22:34349000-34349600	Enhancers	Brain Cingulate Gyrus	brain
18	chr22:34349200-34349400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr22:34349200-34353600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr22:34351600-34358200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr22:34352800-34353600	Enhancers	Primary B cells from peripheral blood	blood
22	chr22:34353400-34353800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr22:34353600-34354600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr22:34353600-34354800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr22:34353800-34354200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr22:34354200-34354800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr22:34354200-34355000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr22:34354200-34355000	Enhancers	Adipose Nuclei	Adipose
29	chr22:34354600-34355000	Enhancers	Primary B cells from peripheral blood	blood
30	chr22:34354800-34355800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr22:34355000-34358400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr22:34355800-34356400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr22:34358200-34358400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr22:34358400-34358800	Enhancers	Primary B cells from peripheral blood	blood
35	chr22:34360000-34361400	Enhancers	Fetal Stomach	stomach
36	chr22:34360600-34360800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr22:34361200-34364600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr22:34364200-34365400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr22:34364600-34364800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr22:34364800-34365600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr22:34364800-34367600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr22:34365200-34365400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr22:34365200-34365600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr22:34365400-34365600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr22:34365400-34365600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr22:34365400-34365600	Enhancers	Fetal Kidney	kidney
47	chr22:34365400-34369200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr22:34365600-34366400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr22:34365600-34367400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr22:34365600-34367600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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