Variant report

Variant	rs2054710
Chromosome Location	chr3:161090616-161090617
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	KAP1	chr3:161090525-161091077	U2OS	brain:	n/a	n/a
2	CTCF	chr3:161090500-161090650	SK-N-SH_RA	brain:	n/a	n/a
3	ZNF263	chr3:161089067-161091165	HEK293-T-REx	kidney:	n/a	chr3:161089773-161089782
4	POLR2A	chr3:161090205-161091055	H1-neurons	neurons:	n/a	n/a
5	TCF7L2	chr3:161089977-161090931	HCT-116	colon:	n/a	n/a
6	GABPA	chr3:161089095-161091343	MCF-7	breast:	n/a	n/a
7	POLR2A	chr3:161090300-161090946	H1-hESC	embryonic stem cell:	n/a	n/a
8	MYC	chr3:161090128-161090974	MCF-7	breast:	n/a	n/a
9	MYC	chr3:161090585-161090990	MCF-7	breast:	n/a	n/a
10	HDAC2	chr3:161089058-161091208	MCF-7	breast:	n/a	chr3:161089632-161089651
11	TAF1	chr3:161090579-161090847	SK-N-SH	brain:	n/a	n/a
12	MAX	chr3:161090191-161091065	H1-hESC	embryonic stem cell:	n/a	n/a
13	GATA2	chr3:161089240-161091190	SH-SY5Y	brain:	n/a	chr3:161089781-161089790 chr3:161090986-161090996
14	EP300	chr3:161089035-161091712	MCF-7	breast:	n/a	chr3:161089801-161089817
15	MYC	chr3:161090270-161090813	H1-hESC	embryonic stem cell:	n/a	n/a
16	TAF1	chr3:161088106-161091184	MCF-7	breast:	n/a	n/a
17	E2F6	chr3:161089363-161091367	H1-hESC	embryonic stem cell:	n/a	n/a
18	GTF2F1	chr3:161090465-161091202	H1-hESC	embryonic stem cell:	n/a	n/a
19	KAP1	chr3:161090311-161091015	HEK293	kidney:	n/a	n/a
20	REST	chr3:161089278-161091161	H1-neurons	neurons:	n/a	n/a
21	POLR2A	chr3:161090360-161091069	H1-hESC	embryonic stem cell:	n/a	n/a
22	FOSL2	chr3:161089080-161091306	MCF-7	breast:	n/a	chr3:161090986-161090995
23	EGR1	chr3:161089059-161091222	MCF-7	breast:	n/a	chr3:161089796-161089809 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089416-161089438 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089420-161089434 chr3:161090857-161090864
24	CTCF	chr3:161089261-161091003	SK-N-SH	brain:	n/a	n/a
25	MAX	chr3:161089450-161091170	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:161090277-161090831	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr3:161088975-161091192	MCF-7	breast:	n/a	n/a
28	GABPA	chr3:161089048-161091265	MCF-7	breast:	n/a	n/a
29	ELF1	chr3:161089077-161091484	MCF-7	breast:	n/a	n/a
30	JUND	chr3:161089053-161091014	MCF-7	breast:	n/a	chr3:161090986-161090995
31	PML	chr3:161089034-161091298	MCF-7	breast:	n/a	n/a
32	RAD21	chr3:161089006-161091074	MCF-7	breast:	n/a	n/a
33	MAFK	chr3:161090583-161090858	H1-hESC	embryonic stem cell:	n/a	chr3:161090660-161090674 chr3:161090659-161090675
34	TCF12	chr3:161088987-161091243	MCF-7	breast:	n/a	n/a
35	SIN3A	chr3:161089119-161091303	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr3:161089003-161091383	MCF-7	breast:	n/a	chr3:161089343-161089353
37	ZNF217	chr3:161090490-161091054	MCF-7	breast:	n/a	n/a
38	GATA3	chr3:161090008-161091098	T-47D	breast:	n/a	chr3:161090986-161090996
39	FOXM1	chr3:161089001-161091338	MCF-7	breast:	n/a	n/a
40	POLR2A	chr3:161088958-161091206	MCF-7	breast:	n/a	n/a
41	POLR2A	chr3:161089036-161091199	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr3:161090436-161090868	H1-hESC	embryonic stem cell:	n/a	n/a
43	TCF12	chr3:161088830-161091241	MCF-7	breast:	n/a	n/a
44	MXI1	chr3:161089108-161091187	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr3:161084726-161091997	MCF-7	breast:	n/a	n/a
46	POLR2A	chr3:161090358-161091071	HCT-116	colon:	n/a	n/a
47	REST	chr3:161089041-161091357	MCF-7	breast:	n/a	n/a
48	GATA3	chr3:161090475-161091102	T-47D	breast:	n/a	chr3:161090986-161090996
49	POLR2A	chr3:161088984-161091224	ProgFib	skin:	n/a	n/a
50	MAX	chr3:161089022-161091279	MCF-7	breast:	n/a	chr3:161089343-161089353

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:161089815..161091859-chr5:87970263..87972091,2	MCF-7	breast:
2	chr3:161038392..161046344-chr3:161085640..161093564,25	MCF-7	breast:
3	chr3:160934982..160947568-chr3:161079696..161093037,40	MCF-7	breast:
4	chr20:45982415..45984680-chr3:161089076..161091449,2	MCF-7	breast:
5	chr3:136470318..136472005-chr3:161088059..161090755,2	MCF-7	breast:
6	chr3:160936365..160960187-chr3:161078472..161094658,51	MCF-7	breast:
7	chr2:97535160..97536953-chr3:161088031..161090726,2	MCF-7	breast:
8	chr3:161090533..161094064-chr8:101963094..101965869,3	MCF-7	breast:
9	chr3:161089431..161091438-chr6:26196434..26199354,2	MCF-7	breast:
10	chr17:57916984..57919121-chr3:161089806..161091709,2	MCF-7	breast:
11	chr3:161088166..161091113-chr7:44082932..44085823,2	MCF-7	breast:
12	chr3:161089882..161091893-chr9:14313286..14315891,2	MCF-7	breast:
13	chr12:48212981..48215317-chr3:161089373..161090906,2	MCF-7	breast:
14	chr3:160282384..160284279-chr3:161090070..161092453,3	MCF-7	breast:
15	chr11:65265519..65268230-chr3:161089523..161091817,2	MCF-7	breast:
16	chr3:160813033..160824577-chr3:161083489..161092050,35	MCF-7	breast:
17	chr3:160472518..160475131-chr3:161089184..161091851,3	MCF-7	breast:
18	chr14:38061358..38063507-chr3:161089489..161091930,2	MCF-7	breast:
19	chr21:46347538..46349062-chr3:161090013..161091580,2	MCF-7	breast:
20	chr17:57913968..57916411-chr3:161089503..161091564,2	MCF-7	breast:
21	chr22:30683032..30685513-chr3:161089094..161092006,2	MCF-7	breast:
22	chr14:73955822..73958124-chr3:161089151..161090979,2	MCF-7	breast:
23	chr20:49346270..49349571-chr3:161087854..161090885,3	MCF-7	breast:
24	chr20:56282039..56284863-chr3:161089358..161091881,2	MCF-7	breast:
25	chr3:160166836..160169216-chr3:161090028..161092220,2	MCF-7	breast:
26	chr3:161088340..161091318-chr9:131938931..131941651,2	MCF-7	breast:
27	chr3:160587600..160589495-chr3:161088974..161091016,2	MCF-7	breast:
28	chr3:161087820..161090854-chr7:26238154..26241381,3	MCF-7	breast:
29	chr10:120838911..120840842-chr3:161089603..161091169,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPTSSB	TF binding region
ENSG00000062716	Chromatin interaction
ENSG00000245864	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000160255	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000122565	Chromatin interaction
ENSG00000164924	Chromatin interaction
ENSG00000240138	Chromatin interaction
ENSG00000107581	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000188483	Chromatin interaction
ENSG00000271052	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000061273	Chromatin interaction
ENSG00000229320	Chromatin interaction
ENSG00000255242	Chromatin interaction
ENSG00000163590	Chromatin interaction
ENSG00000147862	Chromatin interaction
ENSG00000213186	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000124225	Chromatin interaction
ENSG00000170468	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000169251	Chromatin interaction
ENSG00000122566	Chromatin interaction
ENSG00000186432	Chromatin interaction
ENSG00000169255	Chromatin interaction
ENSG00000118007	Chromatin interaction
ENSG00000239282	Chromatin interaction
ENSG00000136279	Chromatin interaction
ENSG00000204055	Chromatin interaction
ENSG00000168758	Chromatin interaction
ENSG00000261758	Chromatin interaction
ENSG00000260572	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10513564	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10936227	0.81[CEU][hapmap]
rs11710086	0.82[CHB][hapmap]
rs11710489	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11710916	0.82[CHB][hapmap];0.84[GIH][hapmap]
rs11711413	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11711695	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11715591	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11718905	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11929238	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13059340	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13059386	0.89[EUR][1000 genomes]
rs13062740	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13073147	1.00[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13076251	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13084731	0.88[EUR][1000 genomes]
rs13084746	0.88[EUR][1000 genomes]
rs1349352	0.81[CHB][hapmap]
rs1382429	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1450519	0.81[CEU][hapmap]
rs1450521	0.88[EUR][1000 genomes]
rs1450522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1450523	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs1478566	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16832082	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16832279	0.82[CHB][hapmap];0.84[GIH][hapmap]
rs1811483	0.83[GIH][hapmap]
rs2100238	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2122527	0.85[EUR][1000 genomes]
rs2404341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404342	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34016896	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34771618	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34896809	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34972965	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35100811	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35310734	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35462273	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4493447	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4856700	0.81[CHB][hapmap]
rs4856701	0.81[CEU][hapmap]
rs4856703	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4856756	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4856757	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4856769	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60625846	0.88[EUR][1000 genomes]
rs6441374	0.84[CEU][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66508859	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67460515	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6772723	0.84[CHD][hapmap]
rs6780536	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73026974	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73026976	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7610800	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7610985	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7630356	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7647118	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7647374	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7648279	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9844862	0.96[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv877710	chr3:161087857-161245414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs2054710	C3orf57	cis	parietal	SCAN
rs2054710	SPTSSB	cis	Thyroid	GTEx
rs2054710	SPTSSB	cis	Heart Left Ventricle	GTEx
rs2054710	SPTSSB	cis	Nerve Tibial	GTEx
rs2054710	B3GALNT1	cis	lymphoblastoid	seeQTL
rs2054710	B3GALT3	cis	multi-tissue	Pritchard
rs2054710	NMD3	cis	parietal	SCAN
rs2054710	B3GALNT1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161088000-161091400	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr3:161088400-161091000	Active TSS	H9 Cell Line	embryonic stem cell
3	chr3:161088600-161090800	Active TSS	Stomach Mucosa	stomach
4	chr3:161089000-161090800	Active TSS	Brain Germinal Matrix	brain
5	chr3:161089000-161091000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:161089000-161091000	Active TSS	Brain Cingulate Gyrus	brain
7	chr3:161089200-161090800	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr3:161089200-161090800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr3:161089200-161090800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:161089200-161090800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
11	chr3:161089200-161090800	Bivalent/Poised TSS	A549	lung
12	chr3:161089200-161090800	Flanking Active TSS	HMEC	breast
13	chr3:161089200-161091000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:161089200-161091000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr3:161089200-161091000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
17	chr3:161089200-161091000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
19	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:161089200-161091000	Active TSS	Esophagus	oesophagus
23	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
24	chr3:161089200-161091000	Bivalent/Poised TSS	Fetal Kidney	kidney
25	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
26	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
27	chr3:161089200-161091000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
28	chr3:161089200-161091200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:161089200-161091200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr3:161089200-161091200	Active TSS	Brain Angular Gyrus	brain
31	chr3:161089200-161091200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
32	chr3:161089400-161090800	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:161089400-161090800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
34	chr3:161089400-161090800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
35	chr3:161089400-161090800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:161089400-161090800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
37	chr3:161089400-161090800	Flanking Bivalent TSS/Enh	Placenta	Placenta
38	chr3:161089400-161090800	Flanking Bivalent TSS/Enh	Osteobl	bone
39	chr3:161089400-161091000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:161089400-161091000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
41	chr3:161089400-161091000	Active TSS	Aorta	Aorta
42	chr3:161089400-161091000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
43	chr3:161089400-161091000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
44	chr3:161089400-161091000	Flanking Active TSS	Pancreas	Pancrea
45	chr3:161089600-161090800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr3:161089600-161090800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:161089600-161090800	Active TSS	Brain Substantia Nigra	brain
48	chr3:161089600-161090800	Active TSS	NHLF	lung
49	chr3:161089600-161091000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
50	chr3:161089600-161091000	Bivalent/Poised TSS	HSMM	muscle

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