Variant report

Variant	rs4718273
Chromosome Location	chr7:65216099-65216100
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	MXI1	chr7:65215538-65216746	HepG2	liver:	n/a	n/a
2	MYC	chr7:65215362-65216746	K562	blood:	n/a	chr7:65216346-65216356 chr7:65216452-65216461
3	GABPA	chr7:65215706-65216231	K562	blood:	n/a	n/a
4	NRF1	chr7:65215640-65216242	GM12878	blood:	n/a	n/a
5	YY1	chr7:65215555-65216603	GM12892	blood:	n/a	chr7:65216273-65216284 chr7:65215992-65216001 chr7:65216296-65216310
6	SP2	chr7:65215715-65216192	HepG2	liver:	n/a	chr7:65215915-65215930 chr7:65215952-65215962
7	RCOR1	chr7:65215312-65216257	GM12878	blood:	n/a	n/a
8	TBL1XR1	chr7:65215488-65216220	K562	blood:	n/a	n/a
9	MYC	chr7:65215325-65216864	K562	blood:	n/a	chr7:65216346-65216356 chr7:65216452-65216461
10	STAT5A	chr7:65215227-65216785	GM12878	blood:	n/a	chr7:65216543-65216555 chr7:65216010-65216022 chr7:65215743-65215755
11	MYC	chr7:65215875-65216150	MCF-7	breast:	n/a	n/a
12	ZBTB7A	chr7:65215596-65216455	K562	blood:	n/a	n/a
13	SP1	chr7:65215593-65216272	H1-hESC	embryonic stem cell:	n/a	chr7:65215919-65215930 chr7:65215950-65215971 chr7:65215916-65215930 chr7:65216010-65216019
14	MYC	chr7:65215849-65216206	K562	blood:	n/a	n/a
15	MAX	chr7:65215179-65216480	HepG2	liver:	n/a	chr7:65216346-65216356 chr7:65216452-65216461 chr7:65215302-65215313 chr7:65215298-65215317
16	POLR2A	chr7:65215476-65216749	U87	brain:	n/a	n/a
17	SP1	chr7:65215681-65216126	H1-hESC	embryonic stem cell:	n/a	chr7:65215919-65215930 chr7:65215950-65215971 chr7:65215916-65215930 chr7:65216010-65216019
18	GATA1	chr7:65215265-65216705	PBDE	blood:	n/a	chr7:65216690-65216701
19	POLR2A	chr7:65215453-65216777	Raji	blood:	n/a	n/a
20	POLR2A	chr7:65215493-65216368	HUVEC	blood vessel:	n/a	n/a
21	TBP	chr7:65215394-65216863	K562	blood:	n/a	n/a
22	POLR2A	chr7:65215341-65216908	GM12878	blood:	n/a	n/a
23	YY1	chr7:65215534-65216552	ECC-1	luminal epithelium:	n/a	chr7:65216273-65216284 chr7:65215992-65216001 chr7:65216296-65216310
24	POLR2A	chr7:65215276-65216310	SK-N-SH	brain:	n/a	n/a
25	YY1	chr7:65215331-65216413	SK-N-SH	brain:	n/a	chr7:65216273-65216284 chr7:65215992-65216001 chr7:65216296-65216310
26	CHD2	chr7:65215320-65216280	Hela-S3	cervix:	n/a	n/a
27	GABPA	chr7:65215549-65216394	A549	lung:	n/a	n/a
28	POLR2A	chr7:65215368-65216505	H1-neurons	neurons:	n/a	n/a
29	MAFK	chr7:65215379-65216182	K562	blood:	n/a	chr7:65215497-65215507
30	MAX	chr7:65215167-65216684	SK-N-SH	brain:	n/a	chr7:65216346-65216356 chr7:65216452-65216461 chr7:65215302-65215313 chr7:65215298-65215317
31	CREB1	chr7:65215658-65216323	A549	lung:	n/a	n/a
32	POLR2A	chr7:65215521-65216303	HEK293	kidney:	n/a	n/a
33	MAX	chr7:65215399-65216530	K562	blood:	n/a	chr7:65216346-65216356 chr7:65216452-65216461
34	POLR2A	chr7:65215670-65216216	A549	lung:	n/a	n/a
35	TAF1	chr7:65215482-65216304	SK-N-SH	brain:	n/a	n/a
36	CHD1	chr7:65216086-65216288	GM12878	blood:	n/a	n/a
37	YY1	chr7:65215666-65216360	ECC-1	luminal epithelium:	n/a	chr7:65216273-65216284 chr7:65215992-65216001 chr7:65216296-65216310
38	HDAC2	chr7:65215622-65216109	HepG2	liver:	n/a	n/a
39	POLR2A	chr7:65215627-65216274	SK-N-SH	brain:	n/a	n/a
40	POU2F2	chr7:65215509-65216099	GM12891	blood:	n/a	n/a
41	HMGN3	chr7:65215664-65216507	K562	blood:	n/a	n/a
42	SP1	chr7:65215523-65216418	A549	lung:	n/a	chr7:65215919-65215930 chr7:65215950-65215971 chr7:65215916-65215930 chr7:65216010-65216019
43	MYC	chr7:65215456-65216429	K562	blood:	n/a	chr7:65216346-65216356
44	ELF1	chr7:65215530-65216341	K562	blood:	n/a	chr7:65215961-65215973
45	MYC	chr7:65215294-65216250	MCF10A-Er-Src	breast:	n/a	chr7:65215302-65215313 chr7:65215298-65215317
46	TAF1	chr7:65215175-65216707	H1-hESC	embryonic stem cell:	n/a	n/a
47	REST	chr7:65215477-65216480	HL-60	blood:	n/a	chr7:65216297-65216310
48	POLR2A	chr7:65215306-65216887	GM12891	blood:	n/a	n/a
49	SMC3	chr7:65215487-65216205	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr7:65215295-65217319	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:56119066..56119592-chr7:65215980..65216673,2	NB4	blood:
2	chr7:56118943..56119510-chr7:65215074..65216153,3	Hela-S3	cervix:
3	chr7:65214353..65216355-chr7:65219585..65221583,2	MCF-7	breast:
4	chr17:36905631..36906196-chr7:65215687..65216448,2	HCT-116	colon:
5	chr6:43596110..43596714-chr7:65215596..65216445,2	NB4	blood:
6	chr7:65214366..65217502-chr7:65337041..65339664,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VKORC1L1-7	chr7:65215736-65216265	NONHSAT147565

Variant related genes	Relation type
CCT6P1	TF binding region
SNORA22	TF binding region
ENSG00000056661	Chromatin interaction
ENSG00000196715	Chromatin interaction
ENSG00000172432	Chromatin interaction
ENSG00000206634	Chromatin interaction
ENSG00000146733	Chromatin interaction
ENSG00000146731	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10247899	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10250008	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10279930	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11971971	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12698508	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs13235246	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13236109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13239979	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs1851840	0.91[CEU][hapmap]
rs2007312	0.81[EUR][1000 genomes]
rs2272185	0.88[ASN][1000 genomes]
rs2419433	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2419434	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2690405	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2900904	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34136756	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs34193460	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs34529418	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34637256	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs34933526	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs35310401	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs35391607	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs35480979	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs35735127	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3734912	0.90[ASN][1000 genomes]
rs3813708	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4718267	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4718269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4718270	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4718274	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4718276	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4718277	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460260	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6460261	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6949812	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs6970243	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7781958	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7789975	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7792846	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7793966	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7794661	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7795242	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9768509	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517778	chr7:64462326-65326821	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv429767	chr7:64473713-65415647	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv917231	chr7:64478253-65300317	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv1029796	chr7:64494934-65302696	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	esv3339156	chr7:64510176-65349050	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	esv2759534	chr7:64551274-65373851	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv427788	chr7:64551274-65390424	Weak transcription Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
8	esv2764020	chr7:64594065-65351820	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv1018447	chr7:64609892-65308719	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv538897	chr7:64609892-65308719	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv1029942	chr7:64679680-65371565	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
12	nsv538903	chr7:64679680-65371565	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
13	nsv1019667	chr7:64679680-65380603	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
14	esv2757227	chr7:64694241-65373851	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
15	nsv1025207	chr7:65092426-65339879	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
16	nsv1033400	chr7:65092426-65339879	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
17	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
18	nsv1020622	chr7:65161364-65339879	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4718273	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs4718273	ASL	cis	multi-tissue	Pritchard
rs4718273	GUSB	cis	Whole Blood	GTEx
rs4718273	RP4-756H11.3	cis	lung	GTEx
rs4718273	VKORC1L1	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65214400-65217200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:65214600-65217000	Active TSS	Hela-S3	cervix
3	chr7:65214800-65217200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:65214800-65217200	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr7:65214800-65217200	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr7:65214800-65217200	Active TSS	HMEC	breast
7	chr7:65214800-65217400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:65215000-65217000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:65215000-65217000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr7:65215000-65217200	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr7:65215000-65217200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:65215000-65217200	Active TSS	Brain Anterior Caudate	brain
13	chr7:65215000-65217200	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr7:65215000-65217200	Active TSS	Rectal Smooth Muscle	rectum
15	chr7:65215000-65217200	Active TSS	A549	lung
16	chr7:65215000-65217200	Active TSS	HSMM	muscle
17	chr7:65215000-65217200	Active TSS	K562	blood
18	chr7:65215000-65217200	Active TSS	NHLF	lung
19	chr7:65215000-65217400	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr7:65215000-65217400	Active TSS	H9 Cell Line	embryonic stem cell
21	chr7:65215000-65217400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:65215000-65217400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr7:65215000-65217400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr7:65215000-65217400	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr7:65215000-65217400	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:65215000-65217600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:65215000-65217800	Active TSS	Colon Smooth Muscle	Colon
28	chr7:65215000-65218600	Active TSS	GM12878-XiMat	blood
29	chr7:65215000-65219600	Active TSS	Stomach Smooth Muscle	stomach
30	chr7:65215200-65217000	Active TSS	Right Ventricle	heart
31	chr7:65215200-65217200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:65215200-65217200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:65215200-65217200	Active TSS	Brain Substantia Nigra	brain
34	chr7:65215200-65217200	Active TSS	Esophagus	oesophagus
35	chr7:65215200-65217200	Active TSS	Fetal Intestine Small	intestine
36	chr7:65215200-65217200	Active TSS	Ovary	ovary
37	chr7:65215200-65217200	Active TSS	Psoas Muscle	Psoas
38	chr7:65215200-65217200	Active TSS	HSMMtube	muscle
39	chr7:65215200-65217400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:65215200-65217400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:65215200-65217400	Active TSS	Fetal Kidney	kidney
42	chr7:65215200-65217600	Active TSS	H1 Cell Line	embryonic stem cell
43	chr7:65215400-65216600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr7:65215400-65216600	Active TSS	Stomach Mucosa	stomach
45	chr7:65215400-65216600	Active TSS	Spleen	Spleen
46	chr7:65215400-65216800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:65215400-65216800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:65215400-65216800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:65215400-65216800	Active TSS	Aorta	Aorta
50	chr7:65215400-65216800	Active TSS	Brain Hippocampus Middle	brain

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