Variant report

Variant	rs385715
Chromosome Location	chr4:2795654-2795655
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	MAZ	chr4:2795378-2795888	GM12878	blood:	n/a	n/a
2	POLR2A	chr4:2795260-2795696	MCF10A-Er-Src	breast:	n/a	n/a
3	JUND	chr4:2795353-2796034	K562	blood:	n/a	n/a
4	POLR2A	chr4:2795465-2796130	HepG2	liver:	n/a	n/a
5	MAX	chr4:2795255-2796216	K562	blood:	n/a	chr4:2795869-2795879
6	SMARCB1	chr4:2794940-2796147	Hela-S3	cervix:	n/a	n/a
7	HA-E2F1	chr4:2795297-2796155	MCF-7	breast:	n/a	chr4:2795620-2795627 chr4:2795566-2795578 chr4:2795620-2795627 chr4:2795620-2795627 chr4:2795566-2795575
8	CEBPB	chr4:2795497-2796322	Hela-S3	cervix:	n/a	chr4:2795902-2795913
9	MYC	chr4:2795469-2796608	MCF10A-Er-Src	breast:	n/a	chr4:2795869-2795879
10	MAZ	chr4:2795172-2797101	IMR90	lung:	n/a	chr4:2796846-2796857
11	MAX	chr4:2795344-2796804	A549	lung:	n/a	chr4:2795869-2795879
12	TFAP2A	chr4:2795374-2796862	Hela-S3	cervix:	n/a	chr4:2796410-2796422 chr4:2796538-2796547 chr4:2795930-2795945
13	ZMIZ1	chr4:2795424-2795898	K562	blood:	n/a	n/a
14	POLR2A	chr4:2795593-2796415	Hela-S3	cervix:	n/a	n/a
15	EP300	chr4:2795359-2797144	SK-N-SH	brain:	n/a	n/a
16	ZNF143	chr4:2795317-2795678	GM12878	blood:	n/a	n/a
17	POLR2A	chr4:2795202-2796999	U87	brain:	n/a	n/a
18	MAX	chr4:2795346-2797194	HepG2	liver:	n/a	chr4:2795869-2795879 chr4:2796846-2796857
19	TEAD4	chr4:2795291-2795893	K562	blood:	n/a	n/a
20	MAX	chr4:2795356-2796286	HepG2	liver:	n/a	chr4:2795869-2795879
21	E2F6	chr4:2795313-2796237	K562	blood:	n/a	chr4:2795620-2795627 chr4:2795566-2795578 chr4:2795620-2795627 chr4:2795620-2795627 chr4:2795566-2795575
22	POLR2A	chr4:2795249-2796837	U87	brain:	n/a	n/a
23	HDAC2	chr4:2795645-2796097	HepG2	liver:	n/a	n/a
24	STAT3	chr4:2795292-2795870	MCF10A-Er-Src	breast:	n/a	chr4:2795392-2795412 chr4:2795392-2795412 chr4:2795390-2795402 chr4:2795397-2795406 chr4:2795398-2795407 chr4:2795398-2795406 chr4:2795396-2795407
25	SMARCC1	chr4:2795173-2796619	Hela-S3	cervix:	n/a	n/a
26	MAX	chr4:2795567-2796047	NB4	blood:	n/a	chr4:2795869-2795879
27	CCNT2	chr4:2795205-2795945	K562	blood:	n/a	chr4:2795566-2795575
28	TBP	chr4:2795559-2796039	HepG2	liver:	n/a	n/a
29	FOS	chr4:2795424-2795981	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F6	chr4:2795571-2795949	K562	blood:	n/a	chr4:2795620-2795627 chr4:2795620-2795627 chr4:2795620-2795627
31	JUN	chr4:2795252-2796109	K562	blood:	n/a	chr4:2795899-2795912
32	ZBTB7A	chr4:2794263-2795708	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr4:2795180-2796858	HL-60	blood:	n/a	n/a
34	STAT1	chr4:2794835-2796475	Hela-S3	cervix:	n/a	chr4:2795392-2795412 chr4:2795392-2795412 chr4:2795390-2795402 chr4:2795397-2795406 chr4:2795396-2795407 chr4:2795398-2795407 chr4:2795398-2795406
35	POLR2A	chr4:2795569-2796337	PANC-1	pancreas:	n/a	n/a
36	POLR2A	chr4:2795208-2796999	U87	brain:	n/a	n/a
37	MAX	chr4:2795191-2797016	A549	lung:	n/a	chr4:2795869-2795879 chr4:2796846-2796857
38	EBF1	chr4:2795470-2795725	GM12878	blood:	n/a	chr4:2795644-2795653
39	RAD21	chr4:2795297-2795745	IMR90	lung:	n/a	n/a
40	EP300	chr4:2795512-2795944	K562	blood:	n/a	n/a
41	UBTF	chr4:2795371-2796225	K562	blood:	n/a	n/a
42	MAFK	chr4:2795461-2796769	Hela-S3	cervix:	n/a	chr4:2796536-2796550 chr4:2796535-2796551 chr4:2796537-2796547 chr4:2796537-2796546 chr4:2796532-2796547 chr4:2796533-2796553
43	CEBPB	chr4:2795519-2796098	IMR90	lung:	n/a	chr4:2795902-2795913
44	MAX	chr4:2795342-2796070	K562	blood:	n/a	chr4:2795869-2795879
45	CREB1	chr4:2795508-2795767	A549	lung:	n/a	n/a
46	CEBPD	chr4:2795565-2796083	HepG2	liver:	n/a	n/a
47	MAZ	chr4:2795612-2796042	HepG2	liver:	n/a	n/a
48	MXI1	chr4:2795445-2796231	HepG2	liver:	n/a	n/a
49	MXI1	chr4:2795440-2796703	Hela-S3	cervix:	n/a	n/a
50	MAX	chr4:2795277-2796682	Hela-S3	cervix:	n/a	chr4:2795869-2795879

No.	Distal block	Cell Line	Cell type
1	chr4:2794178..2796870-chr4:2828744..2832985,4	MCF-7	breast:
2	chr4:2794084..2803742-chr4:2816227..2824357,23	MCF-7	breast:
3	chr17:56708745..56710384-chr4:2792772..2795707,2	MCF-7	breast:
4	chr4:2795447..2803617-chr4:2934606..2939244,18	MCF-7	breast:
5	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
6	chr4:2795244..2797486-chr4:2845439..2847269,2	MCF-7	breast:
7	chr4:2794525..2804465-chr4:2841103..2847851,19	MCF-7	breast:
8	chr4:2793663..2796017-chr4:2810077..2811741,2	MCF-7	breast:
9	chr4:2755902..2759354-chr4:2793552..2797883,6	K562	blood:
10	chr4:2753714..2768807-chr4:2789818..2806638,47	MCF-7	breast:
11	chr4:2757714..2759449-chr4:2793017..2796252,4	K562	blood:
12	chr4:2794820..2799191-chr4:2824314..2827597,4	MCF-7	breast:
13	chr4:2793845..2803067-chr4:2816443..2823671,22	MCF-7	breast:
14	chr4:2747261..2749525-chr4:2793563..2796343,2	K562	blood:

Variant related genes	Relation type
SH3BP2	TF binding region
ENSG00000087269	Chromatin interaction
ENSG00000087266	Chromatin interaction
ENSG00000168884	Chromatin interaction
ENSG00000109736	Chromatin interaction
ENSG00000087274	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000212195	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10011310	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13113803	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13137906	0.80[ASN][1000 genomes]
rs1784148	0.95[CHB][hapmap];0.86[CHD][hapmap];0.80[ASN][1000 genomes]
rs1784149	0.95[CHB][hapmap];0.80[ASN][1000 genomes]
rs2269485	0.80[ASN][1000 genomes]
rs2282770	0.80[ASN][1000 genomes]
rs2282771	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs3213501	0.95[CHB][hapmap];0.88[CHD][hapmap];0.81[ASN][1000 genomes]
rs34993433	0.81[ASN][1000 genomes]
rs370470	0.85[ASN][1000 genomes]
rs393635	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs397292	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs402855	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs407770	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs408102	0.83[ASN][1000 genomes]
rs419096	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs421714	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs422734	1.00[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs426904	1.00[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs433030	1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs445160	0.87[ASN][1000 genomes]
rs450080	1.00[CHB][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6820967	0.86[ASN][1000 genomes]
rs743691	0.87[CHB][hapmap]
rs9685721	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948659	chr4:1828867-2815632	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1005116	chr4:2633935-2812340	Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv470002	chr4:2701098-2836628	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv878445	chr4:2704046-2831383	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv878446	chr4:2710644-2810634	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv878447	chr4:2723531-2831383	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv516797	chr4:2723531-2836628	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv878448	chr4:2723531-2846799	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
12	nsv878449	chr4:2744480-2831383	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1002517	chr4:2747905-2822017	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv967941	chr4:2765555-2802771	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	nsv878452	chr4:2789184-2830076	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv1010533	chr4:2792848-2873441	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
20	esv3439511	chr4:2793779-2796327	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
21	esv3430511	chr4:2794104-2796177	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
22	nsv461162	chr4:2794320-2846799	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	nsv593436	chr4:2794320-2846799	Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs385715	ADD1	cis	lymphoblastoid	seeQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2794400-2795800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr4:2794400-2796000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr4:2794400-2796000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr4:2794800-2795800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:2794800-2796000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
6	chr4:2794800-2796000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr4:2794800-2796200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:2794800-2796400	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr4:2794800-2796400	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr4:2794800-2796400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:2794800-2796400	Flanking Active TSS	Fetal Muscle Leg	muscle
12	chr4:2794800-2796800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:2794800-2797200	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr4:2794800-2797200	Flanking Active TSS	Placenta	Placenta
15	chr4:2795000-2795800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr4:2795000-2795800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:2795000-2795800	Flanking Active TSS	HMEC	breast
18	chr4:2795000-2796000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr4:2795200-2795800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr4:2795200-2795800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:2795200-2795800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
22	chr4:2795200-2796000	Flanking Active TSS	GM12878-XiMat	blood
23	chr4:2795200-2796200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr4:2795200-2796200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr4:2795200-2796200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:2795200-2796800	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr4:2795200-2797000	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr4:2795200-2797200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr4:2795200-2797800	Enhancers	Fetal Heart	heart
30	chr4:2795400-2795800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
31	chr4:2795400-2795800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:2795400-2795800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:2795400-2795800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:2795400-2795800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:2795400-2795800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr4:2795400-2795800	Flanking Active TSS	Fetal Intestine Small	intestine
37	chr4:2795400-2795800	Flanking Active TSS	Fetal Stomach	stomach
38	chr4:2795400-2795800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
39	chr4:2795400-2795800	Flanking Active TSS	Placenta Amnion	Placenta Amnion
40	chr4:2795400-2795800	Flanking Active TSS	Psoas Muscle	Psoas
41	chr4:2795400-2796000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
42	chr4:2795400-2796000	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:2795400-2796000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:2795400-2796000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr4:2795400-2796000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr4:2795400-2796000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr4:2795400-2796000	Flanking Active TSS	Brain Angular Gyrus	brain
48	chr4:2795400-2796000	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr4:2795400-2796000	Flanking Active TSS	Fetal Lung	lung
50	chr4:2795400-2796000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle

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