Variant report

Variant	rs7618915
Chromosome Location	chr3:52279594-52279595
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr3:52278092-52279638	GM12878	blood:	n/a	n/a
2	CHD2	chr3:52279494-52279613	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr3:52278923-52280296	GM19193	blood:	n/a	n/a
4	SIN3AK20	chr3:52279571-52280158	PANC-1	pancreas:	n/a	n/a
5	POU2F2	chr3:52278729-52279638	GM12878	blood:	n/a	n/a
6	POLR2A	chr3:52279565-52280316	HUVEC	blood vessel:	n/a	n/a
7	MAX	chr3:52279453-52280393	H1-hESC	embryonic stem cell:	n/a	chr3:52279824-52279834
8	HDAC2	chr3:52279520-52280062	HepG2	liver:	n/a	n/a
9	CCNT2	chr3:52279514-52280141	K562	blood:	n/a	chr3:52279685-52279694 chr3:52280077-52280086
10	POLR2A	chr3:52279582-52280073	GM12878	blood:	n/a	n/a
11	RCOR1	chr3:52279471-52279671	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr3:52279434-52280252	GM12891	blood:	n/a	n/a
13	HA-E2F1	chr3:52279535-52280287	MCF-7	breast:	n/a	chr3:52279827-52279837
14	TBL1XR1	chr3:52278076-52279621	GM12878	blood:	n/a	n/a
15	RUNX3	chr3:52277852-52279708	GM12878	blood:	n/a	n/a
16	TAF1	chr3:52279467-52280223	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr3:52279555-52280480	HUVEC	blood vessel:	n/a	n/a
18	UBTF	chr3:52279503-52280197	K562	blood:	n/a	n/a
19	POLR2A	chr3:52277921-52279621	GM12892	blood:	n/a	n/a
20	E2F6	chr3:52279451-52280361	H1-hESC	embryonic stem cell:	n/a	chr3:52279827-52279837
21	MAZ	chr3:52279475-52280319	K562	blood:	n/a	chr3:52279824-52279834
22	E2F6	chr3:52279499-52280261	K562	blood:	n/a	chr3:52279827-52279837
23	POLR2A	chr3:52278806-52280260	GM12878	blood:	n/a	n/a
24	POLR2A	chr3:52279203-52280263	GM18951	blood:	n/a	n/a
25	POLR2A	chr3:52277954-52280665	GM12878	blood:	n/a	n/a
26	CHD1	chr3:52279015-52279626	GM12878	blood:	n/a	n/a
27	MAX	chr3:52279337-52280574	H1-hESC	embryonic stem cell:	n/a	chr3:52279824-52279834
28	POLR2A	chr3:52279413-52279749	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:52279495-52280259	HUVEC	blood vessel:	n/a	n/a
30	MAZ	chr3:52278887-52280307	GM12878	blood:	n/a	chr3:52279824-52279834
31	MAX	chr3:52279261-52280339	ECC-1	luminal epithelium:	n/a	chr3:52279824-52279834
32	MXI1	chr3:52279418-52280105	GM12878	blood:	n/a	n/a
33	MAX	chr3:52279391-52280369	SK-N-SH	brain:	n/a	chr3:52279824-52279834
34	POLR2A	chr3:52277713-52280381	GM18505	blood:	n/a	n/a
35	E2F6	chr3:52279428-52280317	K562	blood:	n/a	chr3:52279449-52279459 chr3:52279827-52279837
36	POLR2A	chr3:52279510-52280175	GM10847	blood:	n/a	n/a
37	POLR2A	chr3:52278939-52280285	MCF-7	breast:	n/a	n/a
38	POLR2A	chr3:52278818-52280201	GM12878	blood:	n/a	n/a
39	EBF1	chr3:52277812-52280262	GM12878	blood:	n/a	n/a
40	POLR2A	chr3:52278021-52280334	GM12892	blood:	n/a	n/a
41	ZNF143	chr3:52279526-52280244	H1-hESC	embryonic stem cell:	n/a	chr3:52280120-52280130 chr3:52279672-52279682
42	POLR2A	chr3:52278960-52280260	GM15510	blood:	n/a	n/a
43	POLR2A	chr3:52277951-52280233	GM19099	blood:	n/a	n/a
44	MAX	chr3:52279457-52280385	A549	lung:	n/a	chr3:52279824-52279834
45	MTA3	chr3:52277397-52279759	GM12878	blood:	n/a	n/a
46	POLR2A	chr3:52279055-52280266	GM18526	blood:	n/a	n/a
47	POLR2A	chr3:52278927-52280465	GM12891	blood:	n/a	n/a
48	POLR2A	chr3:52277466-52280409	GM12892	blood:	n/a	n/a
49	YY1	chr3:52278794-52280163	GM12892	blood:	n/a	chr3:52279823-52279834 chr3:52279685-52279696 chr3:52279860-52279874
50	POLR2A	chr3:52279577-52280230	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52279555-52279605	NHDF-neo	bronchial:	n/a
2	chr3:52279555-52279605	GM06990	blood:	n/a
3	chr3:52279555-52279605	Hepatocyte	liver:	n/a
4	chr3:52279555-52279605	HMEC	breast:	n/a
5	chr3:52279555-52279605	NH-A	brain:	n/a
6	chr3:52279555-52279605	GM12878	blood:	n/a
7	chr3:52279555-52279605	SK-N-SH	brain:	n/a
8	chr3:52279555-52279605	AG04450	lung:	fetal
9	chr3:52279555-52279605	Hela-S3	cervix:	n/a
10	chr3:52279555-52279605	PFSK-1	brain:	n/a
11	chr3:52279555-52279605	AG10803	skin:	n/a
12	chr3:52279555-52279605	MCF10A-Er-Src	breast:	n/a
13	chr3:52279555-52279605	U87	brain:	n/a
14	chr3:52279555-52279605	NT2-D1	testis:	n/a
15	chr3:52279555-52279605	MCF-7	breast:	n/a
16	chr3:52279555-52279605	NHBE	bronchial:	n/a
17	chr3:52279555-52279605	SKMC	muscle:	n/a
18	chr3:52279555-52279605	GM12891	blood:	n/a
19	chr3:52279555-52279605	AG09309	skin:	n/a
20	chr3:52279555-52279605	HCM	heart:	n/a
21	chr3:52279555-52279605	BE2_C	brain:	n/a
22	chr3:52279555-52279605	ECC-1	luminal epithelium:	n/a
23	chr3:52279555-52279605	SK-N-SH_RA	brain:	n/a
24	chr3:52279555-52279605	SK-N-MC	brain:	n/a
25	chr3:52279555-52279605	HAEpiC	amniotic membrane:	n/a
26	chr3:52279555-52279605	HEK293	kidney:	embryo
27	chr3:52279555-52279605	K562	blood:	n/a
28	chr3:52279555-52279605	HNPCEpiC	eye:	n/a
29	chr3:52279555-52279605	HepG2	liver:	n/a
30	chr3:52279555-52279605	IMR90	lung:	fetal
31	chr3:52279555-52279605	A549	lung:	n/a
32	chr3:52279555-52279605	AG04449	skin:	fetal
33	chr3:52279555-52279605	HRCEpiC	kidney:	n/a
34	chr3:52279555-52279605	HCT-116	colon:	n/a
35	chr3:52279555-52279605	H1-hESC	embryonic stem cell:	embryo
36	chr3:52279555-52279605	HL-60	blood:	n/a
37	chr3:52279555-52279605	NB4	blood:	n/a
38	chr3:52279555-52279605	HCPEpiC	choroid plexus:	n/a
39	chr3:52279555-52279605	AoSMC	blood vessel:	n/a
40	chr3:52279555-52279605	Jurkat	blood:	n/a
41	chr3:52279555-52279605	HCF	heart:	n/a
42	chr3:52279555-52279605	HRPEpiC	eye:	n/a
43	chr3:52279555-52279605	T-47D	breast:	n/a
44	chr3:52279555-52279605	GM12892	blood:	n/a
45	chr3:52279555-52279605	HEEpiC	esophagus:	n/a
46	chr3:52279555-52279605	LNCaP	prostate:	n/a
47	chr3:52279555-52279605	AG09319	gingival:	n/a
48	chr3:52279555-52279605	BJ	skin:	n/a
49	chr3:52279555-52279605	ProgFib	skin:	n/a
50	chr3:52279555-52279605	PrEC	prostate:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr11:62608645..62609618-chr3:52279287..52279787,2	Hela-S3	cervix:
2	chr3:52278055..52281861-chr3:52310588..52314481,6	K562	blood:
3	chr3:52278277..52281486-chr3:52282865..52288389,9	K562	blood:
4	chr3:52278055..52281861-chr3:52310505..52315451,9	K562	blood:
5	chr3:52278407..52281355-chr3:52281666..52283628,3	MCF-7	breast:
6	chr3:52278070..52281652-chr3:52320199..52323338,4	MCF-7	breast:
7	chr3:52278312..52281288-chr3:52312020..52314246,3	MCF-7	breast:

No data

Variant related genes	Relation type
PPM1M	TF binding region
PPM1M	CpG island
ENSG00000164088	Chromatin interaction
ENSG00000164091	Chromatin interaction
ENSG00000168237	Chromatin interaction
ENSG00000133316	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1060330	0.95[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs11712164	0.81[CHB][hapmap]
rs11717383	0.95[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs13094687	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap]
rs1546737	1.00[CEU][hapmap];0.90[GIH][hapmap];0.95[TSI][hapmap];0.87[EUR][1000 genomes]
rs2267847	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2272088	1.00[CEU][hapmap];0.82[CHB][hapmap];0.87[CHD][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap]
rs2276834	0.83[ASN][1000 genomes]
rs34228726	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34569561	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs353547	0.85[CHB][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs3844291	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3852063	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3852064	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs411457	0.81[CHB][hapmap]
rs57615517	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57630131	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59565798	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs610060	0.95[CHB][hapmap];0.83[CHD][hapmap];0.95[JPT][hapmap]
rs6445358	0.95[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs730050	0.85[CHB][hapmap];0.83[CHD][hapmap];0.83[JPT][hapmap]
rs7614727	0.95[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs7622851	0.86[CHB][hapmap];0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs7629072	0.85[ASN][1000 genomes]
rs7641255	0.85[LWK][hapmap]
rs9311474	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519445	chr3:52004317-52367932	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv984541	chr3:52055970-52285682	Genic enhancers Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv470572	chr3:52123313-52350212	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
4	nsv460537	chr3:52148233-52290550	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv590301	chr3:52148233-52290550	Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv508218	chr3:52155869-52290410	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv834694	chr3:52178983-52335821	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	102 gene(s)	inside rSNPs	diseases
8	nsv834695	chr3:52199701-52400577	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	98 gene(s)	inside rSNPs	diseases
9	nsv876787	chr3:52236762-52367932	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	90 gene(s)	inside rSNPs	diseases
10	nsv876788	chr3:52247110-52367932	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	90 gene(s)	inside rSNPs	diseases
11	nsv876789	chr3:52247110-52575831	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
12	nsv876790	chr3:52261382-52286825	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
13	nsv876791	chr3:52269491-52286825	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
14	esv3369308	chr3:52279062-52280960	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Bipolar disorder	22182935	GWAS catalog

mRNA abundance (count:17)

SNP	Gene	Cis/trans	Tissue	Source
rs7618915	FLJ12442	cis	multi-tissue	Pritchard
rs7618915	SPCS1	cis	parietal	SCAN
rs7618915	NT5DC2	Cis_1M	lymphoblastoid	RTeQTL
rs7618915	GNL3	cis	cerebellum	SCAN
rs7618915	ITIH4	cis	cerebellum	SCAN
rs7618915	NT5DC2	cis	parietal	SCAN
rs7618915	NEK4	cis	cerebellum	SCAN
rs7618915	GNL3	cis	parietal	SCAN
rs7618915	GLT8D1	cis	lymphoblastoid	seeQTL
rs7618915	RBM6	cis	cerebellum	SCAN
rs7618915	NT5DC2	cis	lymphoblastoid	seeQTL
rs7618915	ITIH4	cis	lymphoblastoid	seeQTL
rs7618915	ITIH4	cis	parietal	SCAN
rs7618915	CACNA2D3	cis	parietal	SCAN
rs7618915	NEK4	cis	parietal	SCAN
rs7618915	TMEM110	cis	parietal	SCAN
rs7618915	PRKCD	cis	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52277600-52279600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:52277600-52279600	Enhancers	HMEC	breast
3	chr3:52277600-52282000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr3:52278000-52279600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr3:52278000-52279600	Flanking Active TSS	Hela-S3	cervix
6	chr3:52278200-52279600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:52278400-52280600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:52278600-52279600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
9	chr3:52278800-52279600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:52278800-52279600	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr3:52278800-52279600	Flanking Active TSS	Primary T cells from cord blood	blood
12	chr3:52278800-52279600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
13	chr3:52278800-52279600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
14	chr3:52278800-52279600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr3:52278800-52279600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr3:52278800-52279600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr3:52278800-52279600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:52278800-52279600	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr3:52278800-52279600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr3:52278800-52279600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
21	chr3:52278800-52279600	Flanking Active TSS	GM12878-XiMat	blood
22	chr3:52278800-52280800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:52278800-52281400	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr3:52279000-52279600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:52279000-52279600	Flanking Active TSS	Primary B cells from peripheral blood	blood
26	chr3:52279000-52279600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr3:52279000-52279600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr3:52279000-52279600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr3:52279000-52279600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:52279000-52279600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr3:52279000-52279600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr3:52279000-52279600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr3:52279000-52279600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr3:52279000-52279600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:52279000-52279600	Flanking Active TSS	Brain Anterior Caudate	brain
36	chr3:52279000-52279600	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr3:52279000-52279600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
38	chr3:52279000-52279600	Flanking Active TSS	Colonic Mucosa	Colon
39	chr3:52279000-52279600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
40	chr3:52279000-52279600	Flanking Active TSS	Fetal Lung	lung
41	chr3:52279000-52279600	Flanking Active TSS	Fetal Muscle Leg	muscle
42	chr3:52279000-52279600	Flanking Active TSS	Placenta	Placenta
43	chr3:52279000-52279600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr3:52279000-52279600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
45	chr3:52279000-52279600	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr3:52279000-52279600	Flanking Active TSS	Spleen	Spleen
47	chr3:52279000-52279600	Flanking Active TSS	HepG2	liver
48	chr3:52279000-52279800	Flanking Active TSS	Primary hematopoietic stem cells	blood
49	chr3:52279000-52280400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:52279000-52280400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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