Variant report

Variant	esv3521158
Chromosome Location	chr1:241585504-241587527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:119)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:119 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:241587104-241587399	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr1:241586947-241587161	GM12878	blood:	n/a	n/a
3	CHD2	chr1:241587112-241587410	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr1:241587051-241588231	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr1:241587120-241587270	HepG2	liver:	n/a	n/a
6	CTCF	chr1:241587117-241587249	GM19239	blood:	n/a	n/a
7	CTCF	chr1:241587144-241587213	GM19240	blood:	n/a	n/a
8	CTCF	chr1:241587120-241587213	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr1:241587080-241587230	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr1:241587060-241587210	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr1:241587060-241587210	HMEC	breast:	n/a	n/a
12	CTCF	chr1:241587080-241587230	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr1:241587128-241587217	GM12891	blood:	n/a	n/a
14	CTCF	chr1:241587260-241587410	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr1:241587160-241587310	GM12864	blood:	n/a	n/a
16	CTCF	chr1:241587000-241587270	GM12870	blood:	n/a	n/a
17	CTCF	chr1:241587136-241587230	K562	blood:	n/a	n/a
18	CTCF	chr1:241587100-241587250	HRE	kidney:	n/a	n/a
19	CTCF	chr1:241587060-241587210	GM12869	blood:	n/a	n/a
20	CTCF	chr1:241587060-241587210	AG09319	gingival:	n/a	n/a
21	CTCF	chr1:241587080-241587230	GM12868	blood:	n/a	n/a
22	CTCF	chr1:241587065-241587303	Fibrobl	skin:	n/a	n/a
23	CTCF	chr1:241587140-241587290	HPF	lung:	n/a	n/a
24	CTCF	chr1:241587100-241587250	GM12871	blood:	n/a	n/a
25	CTCF	chr1:241587440-241587590	GM12866	blood:	n/a	n/a
26	CTCF	chr1:241587091-241587249	A549	lung:	n/a	n/a
27	CTCF	chr1:241587140-241587290	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:241585440-241585590	AG09319	gingival:	n/a	n/a
29	CTCF	chr1:241587080-241587230	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr1:241587123-241587255	GM10266	blood:	n/a	n/a
31	CTCF	chr1:241587060-241587210	HMF	breast:	n/a	n/a
32	CTCF	chr1:241587092-241587255	GM19238	blood:	n/a	n/a
33	CTCF	chr1:241587100-241587250	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr1:241585480-241585630	HMF	breast:	n/a	n/a
35	CTCF	chr1:241586960-241587110	HAc	cerebellar:	n/a	n/a
36	CTCF	chr1:241587052-241587297	Gliobla	brain:	n/a	n/a
37	CTCF	chr1:241587053-241587215	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:241587080-241587230	RPTEC	kidney:	n/a	n/a
39	CTCF	chr1:241587160-241587310	HMEC	breast:	n/a	n/a
40	CTCF	chr1:241587020-241587170	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:241587080-241587230	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr1:241587100-241587262	K562	blood:	n/a	n/a
43	CTCF	chr1:241587060-241587210	GM12873	blood:	n/a	n/a
44	CTCF	chr1:241587140-241587290	Caco-2	colon:	n/a	n/a
45	CTCF	chr1:241587080-241587230	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:241587100-241587250	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:241587060-241587210	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr1:241587060-241587210	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr1:241587084-241587255	ProgFib	skin:	n/a	n/a
50	CTCF	chr1:241587120-241587270	BJ	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241587126-241587176	IMR90	lung:	fetal
2	chr1:241587234-241587284	GM19239	blood:	n/a
3	chr1:241587126-241587176	HIPEpiC	eye:	n/a
4	chr1:241587493-241587543	NHDF-neo	bronchial:	n/a
5	chr1:241587234-241587284	K562	blood:	n/a
6	chr1:241587126-241587176	HepG2	liver:	n/a
7	chr1:241587493-241587543	HUVEC	blood vessel:	n/a
8	chr1:241587493-241587543	ovcar-3	ovarian:	n/a
9	chr1:241587493-241587543	NT2-D1	testis:	n/a
10	chr1:241587126-241587176	HRCEpiC	kidney:	n/a
11	chr1:241587126-241587176	HCPEpiC	choroid plexus:	n/a
12	chr1:241587234-241587284	MCF-7	breast:	n/a
13	chr1:241587126-241587176	Hepatocyte	liver:	n/a
14	chr1:241587099-241587149	HIPEpiC	eye:	n/a
15	chr1:241587493-241587543	A549	lung:	n/a
16	chr1:241587126-241587176	H1-hESC	embryonic stem cell:	embryo
17	chr1:241587099-241587149	BE2_C	brain:	n/a
18	chr1:241587493-241587543	HEK293	kidney:	embryo
19	chr1:241587234-241587284	BJ	skin:	n/a
20	chr1:241587099-241587149	Hela-S3	cervix:	n/a
21	chr1:241587126-241587176	T-47D	breast:	n/a
22	chr1:241587099-241587149	SAEC	small airway:	n/a
23	chr1:241587126-241587176	BJ	skin:	n/a
24	chr1:241587234-241587284	H1-hESC	embryonic stem cell:	embryo
25	chr1:241587126-241587176	AG09319	gingival:	n/a
26	chr1:241587234-241587284	HEEpiC	esophagus:	n/a
27	chr1:241587099-241587149	HRCEpiC	kidney:	n/a
28	chr1:241587493-241587543	HNPCEpiC	eye:	n/a
29	chr1:241587234-241587284	PrEC	prostate:	n/a
30	chr1:241587126-241587176	SAEC	small airway:	n/a
31	chr1:241587099-241587149	GM19239	blood:	n/a
32	chr1:241587493-241587543	NH-A	brain:	n/a
33	chr1:241587234-241587284	Jurkat	blood:	n/a
34	chr1:241587126-241587176	GM06990	blood:	n/a
35	chr1:241587099-241587149	ECC-1	luminal epithelium:	n/a
36	chr1:241587234-241587284	HRPEpiC	eye:	n/a
37	chr1:241587126-241587176	ProgFib	skin:	n/a
38	chr1:241587099-241587149	Jurkat	blood:	n/a
39	chr1:241587234-241587284	NHBE	bronchial:	n/a
40	chr1:241587493-241587543	SK-N-SH_RA	brain:	n/a
41	chr1:241587099-241587149	AG09319	gingival:	n/a
42	chr1:241587126-241587176	GM12891	blood:	n/a
43	chr1:241587234-241587284	PANC-1	pancreas:	n/a
44	chr1:241587126-241587176	HAEpiC	amniotic membrane:	n/a
45	chr1:241587099-241587149	HL-60	blood:	n/a
46	chr1:241587493-241587543	AG04449	skin:	fetal
47	chr1:241587493-241587543	HepG2	liver:	n/a
48	chr1:241587493-241587543	SK-N-MC	brain:	n/a
49	chr1:241587234-241587284	HCF	heart:	n/a
50	chr1:241587126-241587176	HNPCEpiC	eye:	n/a

No data

Variant related genes	Relation type
ENSG00000225554	TF binding region
ENSG00000225554	CpG island

Extended variants
information (count: 89 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570629701	chr1:241585507-241585508	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs5012572	chr1:241585523-241585524	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561082793	chr1:241585590-241585591	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186721532	chr1:241585624-241585625	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs76483095	chr1:241585661-241585662	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs560106897	chr1:241585692-241585693	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12037737	chr1:241585725-241585726	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs57443902	chr1:241585731-241585732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs1539099	chr1:241585802-241585803	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs138175512	chr1:241585899-241585900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115731499	chr1:241585904-241585905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191323251	chr1:241585921-241585922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12094986	chr1:241585974-241585975	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs77303602	chr1:241586003-241586004	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs1539100	chr1:241586018-241586019	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs57789558	chr1:241586033-241586034	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs371351587	chr1:241586063-241586064	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs527544331	chr1:241586066-241586067	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs547357470	chr1:241586069-241586070	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs570537078	chr1:241586100-241586101	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs539448200	chr1:241586101-241586102	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs1539101	chr1:241586108-241586109	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs527728451	chr1:241586143-241586144	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569776560	chr1:241586157-241586158	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs112886680	chr1:241586163-241586164	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116440961	chr1:241586185-241586186	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs572666126	chr1:241586224-241586225	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs5782195	chr1:241586230-241586231	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77541746	chr1:241586247-241586248	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs1539102	chr1:241586280-241586281	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576954568	chr1:241586292-241586293	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs545775029	chr1:241586332-241586333	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs562573061	chr1:241586336-241586337	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs576058045	chr1:241586338-241586339	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs112725506	chr1:241586345-241586346	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs1539103	chr1:241586376-241586377	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184412505	chr1:241586386-241586387	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs146105390	chr1:241586397-241586398	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188104556	chr1:241586425-241586426	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs192713199	chr1:241586446-241586447	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs112225840	chr1:241586458-241586459	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs185273564	chr1:241586461-241586462	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs145931687	chr1:241586463-241586464	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs201308917	chr1:241586488-241586489	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs569838588	chr1:241586515-241586516	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529355908	chr1:241586520-241586521	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs112098876	chr1:241586542-241586543	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs55825634	chr1:241586557-241586558	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566291684	chr1:241586589-241586590	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs114197882	chr1:241586591-241586592	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241574200-241587000	Weak transcription	Gastric	stomach
2	chr1:241577600-241586600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:241578000-241586000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:241582200-241586600	Enhancers	NHDF-Ad	bronchial
5	chr1:241583600-241586000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:241584000-241587000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:241585000-241586600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:241585400-241586800	Enhancers	NHLF	lung
9	chr1:241585600-241585800	Enhancers	Osteobl	bone
10	chr1:241585600-241586400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr1:241585800-241586600	Weak transcription	Osteobl	bone
12	chr1:241586000-241586200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:241586000-241586200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:241586000-241586600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr1:241586000-241586800	Active TSS	Brain Anterior Caudate	brain
16	chr1:241586000-241587000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:241586200-241586800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:241586400-241586600	Enhancers	Fetal Brain Male	brain
19	chr1:241586400-241586800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr1:241586600-241586800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:241586600-241586800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:241586600-241586800	Enhancers	Brain Angular Gyrus	brain
23	chr1:241586600-241586800	Enhancers	Brain Substantia Nigra	brain
24	chr1:241586600-241586800	Flanking Active TSS	NHDF-Ad	bronchial
25	chr1:241586600-241586800	Flanking Active TSS	Osteobl	bone
26	chr1:241586600-241587000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
27	chr1:241586600-241587000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr1:241586600-241587000	Active TSS	Fetal Brain Male	brain
29	chr1:241586600-241587400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:241586600-241588200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:241586600-241588200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:241586600-241588200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:241586600-241588200	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr1:241586800-241587000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
35	chr1:241586800-241587000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:241586800-241587000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr1:241586800-241587000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
38	chr1:241586800-241587000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
39	chr1:241586800-241587000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:241586800-241587000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
41	chr1:241586800-241587000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
42	chr1:241586800-241587000	Active TSS	Brain Hippocampus Middle	brain
43	chr1:241586800-241587000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
44	chr1:241586800-241587000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
45	chr1:241586800-241587000	Bivalent Enhancer	Stomach Mucosa	stomach
46	chr1:241586800-241587000	Bivalent Enhancer	HepG2	liver
47	chr1:241586800-241587000	Active TSS	HMEC	breast
48	chr1:241586800-241587200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr1:241586800-241587200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:241586800-241587200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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