Variant report

Variant	rs2073499
Chromosome Location	chr3:50374293-50374294
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:130)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:130 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr3:50374199-50375883	NB4	blood:	n/a	n/a
2	POLR2A	chr3:50374156-50375497	HUVEC	blood vessel:	n/a	n/a
3	TCF3	chr3:50374258-50375568	GM12878	blood:	n/a	n/a
4	POLR2A	chr3:50374026-50376674	K562	blood:	n/a	n/a
5	POLR2A	chr3:50374112-50375343	MCF10A-Er-Src	breast:	n/a	n/a
6	TBL1XR1	chr3:50374193-50374320	K562	blood:	n/a	n/a
7	POLR2A	chr3:50374056-50375219	Hela-S3	cervix:	n/a	n/a
8	E2F4	chr3:50373981-50375244	MCF10A-Er-Src	breast:	n/a	chr3:50375074-50375085
9	POLR2A	chr3:50373760-50375545	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr3:50374095-50375796	SK-N-MC	brain:	n/a	n/a
11	POLR2A	chr3:50372612-50375820	HL-60	blood:	n/a	n/a
12	SIN3A	chr3:50374029-50375727	GM12878	blood:	n/a	n/a
13	JUND	chr3:50373947-50375754	GM12878	blood:	n/a	n/a
14	POLR2A	chr3:50374236-50375766	GM15510	blood:	n/a	n/a
15	POLR2A	chr3:50374033-50375836	GM12878	blood:	n/a	n/a
16	POLR2A	chr3:50374283-50375383	HepG2	liver:	n/a	n/a
17	POLR2A	chr3:50373521-50375529	Hela-S3	cervix:	n/a	n/a
18	SIN3AK20	chr3:50374256-50375084	PANC-1	pancreas:	n/a	n/a
19	MAX	chr3:50374199-50375649	HCT-116	colon:	n/a	n/a
20	IRF1	chr3:50374279-50375138	K562	blood:	n/a	n/a
21	BATF	chr3:50374139-50374463	GM12878	blood:	n/a	n/a
22	POLR2A	chr3:50374174-50375837	K562	blood:	n/a	n/a
23	ZNF263	chr3:50373836-50375398	HEK293-T-REx	kidney:	n/a	chr3:50374211-50374232
24	POLR2A	chr3:50373847-50376521	GM12892	blood:	n/a	n/a
25	POLR2A	chr3:50373029-50375837	HL-60	blood:	n/a	n/a
26	POLR2A	chr3:50373972-50375941	GM12892	blood:	n/a	n/a
27	POLR2A	chr3:50374219-50375390	HUVEC	blood vessel:	n/a	n/a
28	ELF1	chr3:50374134-50375831	GM12878	blood:	n/a	n/a
29	CREB1	chr3:50374209-50375812	GM12878	blood:	n/a	n/a
30	PAX5	chr3:50374268-50375093	GM12878	blood:	n/a	n/a
31	POLR2A	chr3:50373159-50376884	GM12891	blood:	n/a	n/a
32	MAX	chr3:50374083-50375558	ECC-1	luminal epithelium:	n/a	n/a
33	NFATC1	chr3:50374104-50375497	GM12878	blood:	n/a	n/a
34	BACH1	chr3:50374238-50375656	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAZ	chr3:50374211-50375466	GM12878	blood:	n/a	n/a
36	HA-E2F1	chr3:50374009-50375289	MCF-7	breast:	n/a	n/a
37	SIN3AK20	chr3:50373877-50375174	SK-N-SH	brain:	n/a	n/a
38	JUN	chr3:50373406-50375836	K562	blood:	n/a	chr3:50373697-50373705 chr3:50374964-50374977
39	POLR2A	chr3:50374123-50375832	GM12891	blood:	n/a	n/a
40	POLR2A	chr3:50374271-50375374	HepG2	liver:	n/a	n/a
41	POLR2A	chr3:50373797-50375478	U87	brain:	n/a	n/a
42	POLR2A	chr3:50374002-50375701	ECC-1	luminal epithelium:	n/a	n/a
43	POLR2A	chr3:50374143-50375401	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT5A	chr3:50373858-50374952	GM12878	blood:	n/a	n/a
45	TBP	chr3:50374283-50375764	GM12878	blood:	n/a	n/a
46	CHD1	chr3:50372587-50375626	IMR90	lung:	n/a	n/a
47	POLR2A	chr3:50373212-50375856	GM12892	blood:	n/a	n/a
48	CREB1	chr3:50374260-50375321	A549	lung:	n/a	n/a
49	POLR2A	chr3:50374065-50376741	GM18505	blood:	n/a	n/a
50	HCFC1	chr3:50373499-50375577	Hela-S3	cervix:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50272229..50274587-chr3:50373396..50376334,2	MCF-7	breast:
2	chr3:50310332..50311966-chr3:50374071..50376123,2	MCF-7	breast:
3	chr3:50374237..50374856-chr7:5565993..5566639,2	Hela-S3	cervix:
4	chr3:50325622..50330493-chr3:50373581..50377874,6	K562	blood:
5	chr3:50373336..50376121-chr3:50395555..50398512,4	K562	blood:
6	chr3:50356822..50362778-chr3:50372728..50378128,10	MCF-7	breast:
7	chr3:50371739..50377775-chr3:50378206..50384768,10	MCF-7	breast:
8	chr3:50373346..50376603-chr3:50387024..50392661,8	MCF-7	breast:
9	chr3:50374257..50376540-chr3:50394477..50397107,2	MCF-7	breast:
10	chr10:74032940..74033738-chr3:50373869..50374386,2	Hela-S3	cervix:
11	chr3:50333907..50338508-chr3:50371973..50376030,7	K562	blood:
12	chr3:50372879..50374591-chr3:50450931..50453319,2	MCF-7	breast:
13	chr3:50373715..50376793-chr3:50377375..50380061,4	MCF-7	breast:
14	chr3:50329739..50332601-chr3:50372246..50375675,3	MCF-7	breast:
15	chr3:50335402..50338508-chr3:50371973..50376083,5	K562	blood:
16	chr3:50274751..50276271-chr3:50373939..50375555,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZMYND10-AS1	TF binding region
ENSG00000068001	Chromatin interaction
ENSG00000114395	Chromatin interaction
ENSG00000214706	Chromatin interaction
ENSG00000004838	Chromatin interaction
ENSG00000168209	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000012171	Chromatin interaction
ENSG00000068028	Chromatin interaction
ENSG00000114388	Chromatin interaction
ENSG00000272104	Chromatin interaction
ENSG00000126062	Chromatin interaction
ENSG00000243477	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000235058	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10510755	0.93[CEU][hapmap]
rs1107265	0.85[ASW][hapmap];0.82[MEX][hapmap]
rs11130248	0.84[CHD][hapmap]
rs12054403	0.81[CHB][hapmap];0.84[CHD][hapmap]
rs12485390	0.83[JPT][hapmap]
rs12485909	0.81[CHD][hapmap]
rs12488302	0.81[CHB][hapmap];0.84[CHD][hapmap]
rs12492880	0.84[CHD][hapmap]
rs12494414	0.88[CHD][hapmap];0.87[JPT][hapmap]
rs12494849	0.86[ASW][hapmap]
rs12629572	0.93[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.92[ASN][1000 genomes]
rs1467913	0.80[ASW][hapmap]
rs1467914	0.86[ASW][hapmap]
rs1989839	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[ASN][1000 genomes]
rs2071203	0.84[CHD][hapmap]
rs2071204	0.84[CHD][hapmap]
rs2071802	0.93[CEU][hapmap]
rs2071803	0.93[CEU][hapmap]
rs2073498	0.87[CEU][hapmap]
rs2073500	0.84[CHD][hapmap]
rs2233474	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2233476	0.84[CHD][hapmap]
rs2236939	0.81[CEU][hapmap]
rs2236944	0.84[CHD][hapmap]
rs2236946	0.84[CHD][hapmap];0.82[JPT][hapmap]
rs2236947	0.83[YRI][hapmap]
rs2236948	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2236950	0.84[CHB][hapmap];0.88[CHD][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2236951	0.86[ASW][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2236964	0.85[ASW][hapmap];0.82[MEX][hapmap]
rs2236965	0.85[ASW][hapmap]
rs2236973	0.85[ASW][hapmap]
rs2236979	0.85[ASW][hapmap]
rs2236984	0.85[ASW][hapmap]
rs2236987	0.85[ASW][hapmap]
rs2239801	0.93[CEU][hapmap]
rs2282751	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2282753	0.85[ASW][hapmap];0.82[MEX][hapmap]
rs2282754	0.82[MEX][hapmap]
rs2285043	0.84[CHD][hapmap]
rs2298953	0.81[CHD][hapmap]
rs2298954	0.81[CHD][hapmap]
rs2301639	0.93[CEU][hapmap]
rs28365992	0.93[CEU][hapmap]
rs3213621	0.84[CHD][hapmap]
rs35455589	0.82[CHD][hapmap]
rs35587949	0.84[CHD][hapmap]
rs3774753	0.81[CHD][hapmap]
rs3774755	0.82[CHD][hapmap]
rs3806708	0.93[CEU][hapmap]
rs4141060	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4688682	0.81[CHD][hapmap];0.83[JPT][hapmap]
rs4688732	0.84[CHD][hapmap]
rs4688734	0.84[CHD][hapmap]
rs4688741	0.81[CHD][hapmap]
rs57838764	1.00[ASN][1000 genomes]
rs6776145	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.94[ASN][1000 genomes]
rs6786523	0.80[ASW][hapmap]
rs734767	0.82[MEX][hapmap]
rs739431	0.87[CEU][hapmap];0.96[GIH][hapmap]
rs743756	0.85[ASW][hapmap]
rs743757	0.85[ASW][hapmap];0.82[MEX][hapmap]
rs743857	0.85[ASW][hapmap]
rs762705	0.89[ASN][1000 genomes]
rs7645537	0.81[CHD][hapmap]
rs9835537	0.85[ASW][hapmap]
rs9852677	0.85[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap];0.83[JPT][hapmap];0.83[MEX][hapmap]
rs9883222	0.81[CHD][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
6	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription 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	104 gene(s)	inside rSNPs	diseases
9	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
10	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
11	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
12	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
13	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
14	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
15	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers 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 miRNA target site	83 gene(s)	inside rSNPs	diseases
16	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
17	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
18	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
19	nsv876775	chr3:50324672-50504896	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
20	nsv590258	chr3:50368278-50381022	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
21	esv3584502	chr3:50368278-50659741	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers 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 target site	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2073499	PCBP4	cis	parietal	SCAN
rs2073499	ZNF589	cis	cerebellum	SCAN
rs2073499	TRAIP	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50372800-50374400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr3:50372800-50374400	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr3:50372800-50375400	Active TSS	Right Ventricle	heart
4	chr3:50373000-50374400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:50373000-50374600	Flanking Active TSS	Stomach Smooth Muscle	stomach
6	chr3:50373200-50374400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:50373200-50374400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr3:50373200-50374400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr3:50373200-50374400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:50373200-50374400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr3:50373200-50374400	Flanking Active TSS	Brain Anterior Caudate	brain
12	chr3:50373200-50374400	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr3:50373200-50374400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
14	chr3:50373200-50374400	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr3:50373200-50374400	Flanking Active TSS	Rectal Smooth Muscle	rectum
16	chr3:50373200-50374600	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr3:50373200-50374800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr3:50373400-50374400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:50373400-50374400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
20	chr3:50373400-50374400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:50373400-50374400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
22	chr3:50373400-50374400	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr3:50373400-50374400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
24	chr3:50373400-50374400	Flanking Active TSS	Fetal Muscle Trunk	muscle
25	chr3:50373400-50374400	Flanking Active TSS	Placenta	Placenta
26	chr3:50373400-50374400	Flanking Active TSS	Fetal Thymus	thymus
27	chr3:50373400-50374600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
28	chr3:50373400-50374600	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr3:50373400-50375400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:50373400-50375800	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr3:50373400-50375800	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr3:50373600-50374400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
33	chr3:50373600-50374400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:50373600-50374400	Flanking Active TSS	Liver	Liver
35	chr3:50373600-50374400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr3:50373600-50374400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr3:50373600-50374600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:50373600-50375000	Active TSS	NHLF	lung
39	chr3:50373600-50375200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:50373600-50375200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr3:50373600-50375200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr3:50373600-50375200	Active TSS	Esophagus	oesophagus
43	chr3:50373600-50375400	Active TSS	Gastric	stomach
44	chr3:50373600-50375600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:50373600-50375600	Active TSS	Aorta	Aorta
46	chr3:50373600-50375600	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr3:50373600-50375600	Active TSS	Lung	lung
48	chr3:50373600-50376000	Active TSS	GM12878-XiMat	blood
49	chr3:50373800-50374400	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
50	chr3:50373800-50374400	Flanking Active TSS	Primary T cells from cord blood	blood

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