Variant report

Variant	rs1183245
Chromosome Location	chr7:65541185-65541186
allele	A/G
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	ZNF263	chr7:65540730-65541527	HEK293-T-REx	kidney:	n/a	n/a
2	MXI1	chr7:65540652-65541806	Hela-S3	cervix:	n/a	chr7:65541421-65541430
3	MYC	chr7:65540402-65541949	K562	blood:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
4	TAF1	chr7:65540370-65541220	H1-hESC	embryonic stem cell:	n/a	n/a
5	UBTF	chr7:65540654-65541207	K562	blood:	n/a	n/a
6	CHD2	chr7:65540527-65541379	GM12878	blood:	n/a	n/a
7	MAX	chr7:65540519-65541702	ECC-1	luminal epithelium:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
8	MTA3	chr7:65540593-65541630	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:65540631-65541203	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr7:65540375-65541201	K562	blood:	n/a	n/a
11	RAD21	chr7:65540675-65541212	SK-N-SH_RA	brain:	n/a	chr7:65540803-65540817
12	MXI1	chr7:65540404-65542157	HepG2	liver:	n/a	chr7:65541421-65541430
13	ELF1	chr7:65540414-65542038	GM12878	blood:	n/a	chr7:65540804-65540816
14	CTCF	chr7:65541120-65541270	GM06990	blood:	n/a	n/a
15	CTCF	chr7:65541160-65541310	RPTEC	kidney:	n/a	n/a
16	POLR2A	chr7:65540372-65541389	K562	blood:	n/a	n/a
17	POLR2A	chr7:65540289-65542348	HepG2	liver:	n/a	n/a
18	TAF1	chr7:65540429-65541426	ECC-1	luminal epithelium:	n/a	n/a
19	CTCF	chr7:65541056-65541216	GM12891	blood:	n/a	n/a
20	CTCF	chr7:65541120-65541270	HepG2	liver:	n/a	n/a
21	CTCF	chr7:65541040-65541190	AG04450	lung:	n/a	n/a
22	YY1	chr7:65540649-65541191	GM12891	blood:	n/a	chr7:65541058-65541078
23	YY1	chr7:65540574-65541217	K562	blood:	n/a	chr7:65541058-65541078
24	CTCF	chr7:65541060-65541210	GM12869	blood:	n/a	n/a
25	STAT3	chr7:65541102-65541402	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr7:65540460-65541462	MCF-7	breast:	n/a	n/a
27	RAD21	chr7:65540665-65541396	Hela-S3	cervix:	n/a	chr7:65540803-65540817
28	HDAC2	chr7:65540415-65541549	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:65541120-65541270	K562	blood:	n/a	n/a
30	ZKSCAN1	chr7:65540731-65541405	Hela-S3	cervix:	n/a	n/a
31	MAX	chr7:65540363-65541806	HCT-116	colon:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
32	YY1	chr7:65540609-65541233	GM12892	blood:	n/a	chr7:65541058-65541078
33	MAX	chr7:65540440-65541733	MCF-7	breast:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
34	POLR2A	chr7:65540580-65541198	HL-60	blood:	n/a	n/a
35	CTCF	chr7:65541033-65541216	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:65540940-65541190	GM12874	blood:	n/a	n/a
37	POLR2A	chr7:65540512-65541189	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr7:65541040-65541190	MCF-7	breast:	n/a	n/a
39	SIN3A	chr7:65540388-65541634	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr7:65540884-65541240	GM12878	blood:	n/a	n/a
41	MAX	chr7:65540245-65542175	HepG2	liver:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
42	MAZ	chr7:65540304-65541289	GM12878	blood:	n/a	n/a
43	MXI1	chr7:65539989-65542591	SK-N-SH	brain:	n/a	chr7:65541421-65541430
44	POLR2A	chr7:65540386-65541397	GM18505	blood:	n/a	n/a
45	NFYA	chr7:65540521-65541440	K562	blood:	n/a	n/a
46	POLR2A	chr7:65540488-65541471	MCF-7	breast:	n/a	n/a
47	MAX	chr7:65540485-65542013	NB4	blood:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
48	POLR2A	chr7:65540493-65541237	GM12878	blood:	n/a	n/a
49	MAX	chr7:65540409-65541643	ECC-1	luminal epithelium:	n/a	chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541419-65541430 chr7:65541420-65541429 chr7:65541418-65541431 chr7:65541420-65541430 chr7:65541418-65541431
50	E2F4	chr7:65540307-65541341	K562	blood:	n/a	chr7:65540624-65540636 chr7:65540764-65540774 chr7:65540615-65540624 chr7:65540612-65540624

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65541137-65541187	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:65541137-65541187	MCF10A-Er-Src	breast:	n/a
3	chr7:65541137-65541187	NHBE	bronchial:	n/a
4	chr7:65541137-65541187	HCM	heart:	n/a
5	chr7:65541137-65541187	HAEpiC	amniotic membrane:	n/a
6	chr7:65541137-65541187	U87	brain:	n/a
7	chr7:65541137-65541187	PrEC	prostate:	n/a
8	chr7:65541137-65541187	CMK	blood:	n/a
9	chr7:65541137-65541187	SK-N-SH	brain:	n/a
10	chr7:65541137-65541187	HMEC	breast:	n/a
11	chr7:65541137-65541187	ProgFib	skin:	n/a
12	chr7:65541137-65541187	IMR90	lung:	fetal
13	chr7:65541137-65541187	GM12892	blood:	n/a
14	chr7:65541137-65541187	LNCaP	prostate:	n/a
15	chr7:65541137-65541187	BE2_C	brain:	n/a
16	chr7:65541137-65541187	AG04450	lung:	fetal
17	chr7:65541137-65541187	HRE	kidney:	n/a
18	chr7:65541137-65541187	PFSK-1	brain:	n/a
19	chr7:65541137-65541187	HEK293	kidney:	embryo
20	chr7:65541137-65541187	HEEpiC	esophagus:	n/a
21	chr7:65541137-65541187	SKMC	muscle:	n/a
22	chr7:65541137-65541187	NH-A	brain:	n/a
23	chr7:65541137-65541187	Caco-2	colon:	n/a
24	chr7:65541137-65541187	AG04449	skin:	fetal
25	chr7:65541137-65541187	NB4	blood:	n/a
26	chr7:65541137-65541187	HIPEpiC	eye:	n/a
27	chr7:65541137-65541187	T-47D	breast:	n/a
28	chr7:65541137-65541187	GM12878	blood:	n/a
29	chr7:65541137-65541187	HNPCEpiC	eye:	n/a
30	chr7:65541137-65541187	H1-hESC	embryonic stem cell:	embryo
31	chr7:65541137-65541187	Hela-S3	cervix:	n/a
32	chr7:65541137-65541187	AG10803	skin:	n/a
33	chr7:65541137-65541187	SAEC	small airway:	n/a
34	chr7:65541137-65541187	AoSMC	blood vessel:	n/a
35	chr7:65541137-65541187	Hepatocyte	liver:	n/a
36	chr7:65541137-65541187	ECC-1	luminal epithelium:	n/a
37	chr7:65541137-65541187	HCF	heart:	n/a
38	chr7:65541137-65541187	ovcar-3	ovarian:	n/a
39	chr7:65541137-65541187	MCF-7	breast:	n/a
40	chr7:65541137-65541187	HRPEpiC	eye:	n/a
41	chr7:65541137-65541187	AG09309	skin:	n/a
42	chr7:65541137-65541187	SK-N-MC	brain:	n/a
43	chr7:65541137-65541187	GM19239	blood:	n/a
44	chr7:65541137-65541187	GM12891	blood:	n/a
45	chr7:65541137-65541187	NHDF-neo	bronchial:	n/a
46	chr7:65541137-65541187	AG09319	gingival:	n/a
47	chr7:65541137-65541187	A549	lung:	n/a
48	chr7:65541137-65541187	HL-60	blood:	n/a
49	chr7:65541137-65541187	HUVEC	blood vessel:	n/a
50	chr7:65541137-65541187	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:65540244..65541852-chr7:66118000..66119624,2	K562	blood:
2	chr7:65439470..65441298-chr7:65540371..65542201,2	K562	blood:
3	chr7:65540520..65541322-chrX:20159426..20159971,2	NB4	blood:
4	chr7:65536010..65538329-chr7:65539255..65541774,2	MCF-7	breast:
5	chr7:65538951..65542131-chr7:65578976..65581332,4	MCF-7	breast:
6	chr7:65540799..65542994-chr7:65578683..65581272,2	MCF-7	breast:
7	chr7:65540457..65542538-chr7:65550059..65552910,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000205596	TF binding region
ENSG00000205596	CpG island
ENSG00000126522	Chromatin interaction
ENSG00000169919	Chromatin interaction
ENSG00000205596	Chromatin interaction
ENSG00000226824	Chromatin interaction
ENSG00000249319	Chromatin interaction
ENSG00000173674	Chromatin interaction
ENSG00000241258	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10256544	0.89[CEU][hapmap]
rs10260426	0.89[CEU][hapmap]
rs10282433	0.89[CEU][hapmap]
rs1144894	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1144895	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1167390	0.89[CEU][hapmap]
rs1167395	0.85[AMR][1000 genomes]
rs1167406	0.89[CEU][hapmap]
rs1167411	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1167612	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11760844	0.89[CEU][hapmap]
rs1182882	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11971949	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11974219	0.84[AMR][1000 genomes]
rs11974264	0.85[AMR][1000 genomes]
rs12537823	0.89[CEU][hapmap]
rs13225383	0.82[AMR][1000 genomes]
rs13240492	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13247295	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1540651	0.83[AMR][1000 genomes]
rs1565531	0.82[AMR][1000 genomes]
rs160635	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1875057	0.88[CEU][hapmap]
rs1983372	0.92[CEU][hapmap]
rs2087647	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2220626	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2249458	0.85[CEU][hapmap]
rs2420168	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2949696	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35028832	0.82[AMR][1000 genomes]
rs427557	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs427575	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4718330	0.89[CEU][hapmap]
rs55962648	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs587360	0.89[CEU][hapmap]
rs6460282	0.89[CEU][hapmap]
rs6944374	0.85[CEU][hapmap]
rs6945843	1.00[CEU][hapmap]
rs6946143	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6951503	0.85[CEU][hapmap]
rs6952182	0.89[CEU][hapmap]
rs6957690	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6958484	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6960446	0.89[CEU][hapmap]
rs6961717	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6963646	1.00[CEU][hapmap]
rs6964437	0.89[CEU][hapmap]
rs6971509	1.00[CEU][hapmap]
rs6974614	0.89[CEU][hapmap]
rs697968	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs697969	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs697970	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs709609	0.89[CEU][hapmap];0.81[AMR][1000 genomes]
rs7801282	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs780742	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs780743	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs780744	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs780998	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs809080	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs875971	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs880166	0.89[CEU][hapmap]
rs908915	0.89[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	nsv888325	chr7:65474919-65575893	Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1021186	chr7:65492601-65663438	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv984546	chr7:65531382-65556631	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs1183245	GTF2IRD1P1	cis	Thyroid	GTEx
rs1183245	RP4-756H11.3	cis	Nerve Tibial	GTEx
rs1183245	RP4-756H11.3	cis	Muscle Skeletal	GTEx
rs1183245	RP4-756H11.3	cis	Heart Left Ventricle	GTEx
rs1183245	RNU6-96P	cis	Thyroid	GTEx
rs1183245	GS1-124K5.11	cis	Thyroid	GTEx
rs1183245	RP4-756H11.3	cis	lung	GTEx
rs1183245	RP4-756H11.3	cis	Artery Tibial	GTEx
rs1183245	RP4-756H11.3	cis	Thyroid	GTEx
rs1183245	GS1-124K5.4	cis	Artery Aorta	GTEx
rs1183245	GS1-124K5.4	cis	Stomach	GTEx
rs1183245	RP4-756H11.3	cis	Artery Aorta	GTEx
rs1183245	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs1183245	ASL	Cis_1M	lymphoblastoid	RTeQTL
rs1183245	RP4-756H11.3	cis	Adipose Subcutaneous	GTEx
rs1183245	GS1-124K5.4	cis	Whole Blood	GTEx
rs1183245	RP4-756H11.3	cis	Esophagus Mucosa	GTEx
rs1183245	RP4-756H11.3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65540000-65541200	Active TSS	Fetal Brain Female	brain
2	chr7:65540200-65541200	Active TSS	H1 Cell Line	embryonic stem cell
3	chr7:65540200-65541200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:65540200-65541200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:65540200-65541200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:65540200-65541200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:65540200-65541200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:65540200-65541200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:65540200-65541200	Active TSS	Brain Angular Gyrus	brain
10	chr7:65540200-65541200	Active TSS	Brain Anterior Caudate	brain
11	chr7:65540200-65541200	Active TSS	Brain Cingulate Gyrus	brain
12	chr7:65540200-65541200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:65540200-65541200	Active TSS	Colonic Mucosa	Colon
14	chr7:65540200-65541200	Active TSS	Duodenum Mucosa	Duodenum
15	chr7:65540200-65541200	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr7:65540200-65541200	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr7:65540200-65541200	Active TSS	Rectal Mucosa Donor 31	rectum
18	chr7:65540200-65541200	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr7:65540200-65541200	Active TSS	GM12878-XiMat	blood
20	chr7:65540200-65541200	Active TSS	Hela-S3	cervix
21	chr7:65540200-65541400	Active TSS	H9 Cell Line	embryonic stem cell
22	chr7:65540200-65541400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr7:65540200-65541400	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr7:65540200-65541400	Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr7:65540200-65541400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:65540200-65541400	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr7:65540200-65541400	Active TSS	Brain Hippocampus Middle	brain
28	chr7:65540200-65541400	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr7:65540200-65541400	Active TSS	Fetal Intestine Small	intestine
30	chr7:65540200-65541400	Active TSS	Rectal Smooth Muscle	rectum
31	chr7:65540200-65541400	Active TSS	Stomach Smooth Muscle	stomach
32	chr7:65540200-65541800	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr7:65540200-65542000	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr7:65540200-65542000	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr7:65540200-65542000	Active TSS	A549	lung
36	chr7:65540400-65541200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:65540400-65541200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:65540400-65541200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:65540400-65541200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:65540400-65541200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:65540400-65541200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:65540400-65541200	Active TSS	Primary T cells from cord blood	blood
43	chr7:65540400-65541200	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr7:65540400-65541200	Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr7:65540400-65541200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:65540400-65541200	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr7:65540400-65541200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:65540400-65541200	Active TSS	Colon Smooth Muscle	Colon
49	chr7:65540400-65541200	Active TSS	Esophagus	oesophagus
50	chr7:65540400-65541200	Active TSS	Fetal Heart	heart

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