Variant report

Variant	rs10065689
Chromosome Location	chr5:43604258-43604259
allele	C/T
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	POLR2A	chr5:43602342-43604392	HUVEC	blood vessel:	n/a	n/a
2	ELF1	chr5:43602744-43604408	GM12878	blood:	n/a	chr5:43603385-43603397
3	MYC	chr5:43603882-43604260	MCF-7	breast:	n/a	n/a
4	POLR2A	chr5:43603921-43604320	Hela-S3	cervix:	n/a	n/a
5	MAX	chr5:43602029-43604259	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr5:43602018-43604302	GM12878	blood:	n/a	n/a
7	MYC	chr5:43602468-43604315	NB4	blood:	n/a	n/a
8	RUNX3	chr5:43602789-43604393	GM12878	blood:	n/a	chr5:43603568-43603583
9	POLR2A	chr5:43603043-43604398	MCF-7	breast:	n/a	n/a
10	TBL1XR1	chr5:43604156-43604269	K562	blood:	n/a	n/a
11	MAX	chr5:43602028-43604337	NB4	blood:	n/a	n/a
12	SIN3AK20	chr5:43603882-43604347	PANC-1	pancreas:	n/a	n/a
13	NFYB	chr5:43603964-43604281	Hela-S3	cervix:	n/a	chr5:43604077-43604087 chr5:43604072-43604087 chr5:43604075-43604090 chr5:43604074-43604086 chr5:43604075-43604090
14	POLR2A	chr5:43602032-43604360	GM12892	blood:	n/a	n/a
15	PAX5	chr5:43603896-43604431	GM12878	blood:	n/a	n/a
16	POLR2A	chr5:43603790-43604271	ECC-1	luminal epithelium:	n/a	n/a
17	TEAD4	chr5:43603881-43604367	ECC-1	luminal epithelium:	n/a	n/a
18	MAX	chr5:43603739-43604294	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr5:43602413-43604267	GM12892	blood:	n/a	n/a
20	POLR2A	chr5:43603779-43604313	SK-N-SH	brain:	n/a	n/a
21	POLR2A	chr5:43602398-43604433	HL-60	blood:	n/a	n/a
22	SIN3A	chr5:43602872-43604309	GM12878	blood:	n/a	n/a
23	POLR2A	chr5:43603017-43604351	MCF-7	breast:	n/a	n/a
24	POLR2A	chr5:43602425-43604573	HL-60	blood:	n/a	n/a
25	NFYB	chr5:43603862-43604332	GM12878	blood:	n/a	chr5:43604077-43604087 chr5:43604072-43604087 chr5:43604075-43604090 chr5:43604074-43604086 chr5:43604075-43604090
26	POLR2A	chr5:43604090-43604258	Hela-S3	cervix:	n/a	n/a
27	RFX5	chr5:43601979-43604323	Hela-S3	cervix:	n/a	chr5:43604078-43604087
28	ESR1	chr5:43604014-43604365	T-47D	breast:	n/a	n/a
29	POLR2A	chr5:43602943-43604379	MCF-7	breast:	n/a	n/a
30	POLR2A	chr5:43604067-43604305	MCF10A-Er-Src	breast:	n/a	n/a
31	MXI1	chr5:43601361-43604702	SK-N-SH	brain:	n/a	n/a
32	POLR2A	chr5:43601886-43604310	GM12878	blood:	n/a	n/a
33	FOXA1	chr5:43603912-43604295	T-47D	breast:	n/a	n/a
34	MXI1	chr5:43604169-43604339	Hela-S3	cervix:	n/a	n/a
35	MXI1	chr5:43601813-43604468	IMR90	lung:	n/a	n/a
36	BHLHE40	chr5:43603957-43604285	HepG2	liver:	n/a	n/a
37	GABPA	chr5:43603835-43604312	SK-N-SH	brain:	n/a	n/a
38	POLR2A	chr5:43602382-43604481	GM12878	blood:	n/a	n/a
39	TBP	chr5:43603977-43604260	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr5:43603931-43604474	ProgFib	skin:	n/a	n/a
41	POLR2A	chr5:43602608-43604290	GM10847	blood:	n/a	n/a
42	POLR2A	chr5:43602608-43604443	K562	blood:	n/a	n/a
43	EBF1	chr5:43603731-43604360	GM12878	blood:	n/a	n/a
44	POLR2A	chr5:43601945-43604329	GM12891	blood:	n/a	n/a
45	CHD2	chr5:43603914-43604297	Hela-S3	cervix:	n/a	n/a
46	GTF2F1	chr5:43604131-43604274	H1-hESC	embryonic stem cell:	n/a	n/a
47	TFAP2C	chr5:43602404-43604282	Hela-S3	cervix:	n/a	chr5:43603351-43603366
48	POLR2A	chr5:43602557-43604377	HUVEC	blood vessel:	n/a	n/a
49	BHLHE40	chr5:43603752-43604379	GM12878	blood:	n/a	n/a
50	POLR2A	chr5:43602053-43604374	GM18951	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:43554854..43559895-chr5:43599481..43606699,15	MCF-7	breast:
2	chr5:43482042..43485833-chr5:43601604..43604541,3	MCF-7	breast:
3	chr5:43512794..43515547-chr5:43602190..43604500,3	MCF-7	breast:
4	chr5:43555487..43559521-chr5:43598404..43605405,16	K562	blood:
5	chr5:43552832..43560830-chr5:43598877..43605844,26	MCF-7	breast:
6	chr5:375088..376007-chr5:43603703..43604323,2	NB4	blood:
7	chr5:43481246..43484731-chr5:43603166..43606245,4	K562	blood:
8	chr5:43482483..43486113-chr5:43601084..43606081,7	K562	blood:
9	chr5:43601763..43605743-chr5:43610640..43615837,7	K562	blood:
10	chr5:43601796..43604385-chr5:44808876..44810396,2	K562	blood:
11	chr5:43555382..43559666-chr5:43598979..43604929,17	K562	blood:

Variant related genes	Relation type
NNT-AS1	TF binding region
ENSG00000248240	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000172244	Chromatin interaction
ENSG00000251141	Chromatin interaction
ENSG00000112992	Chromatin interaction
ENSG00000112996	Chromatin interaction
ENSG00000172239	Chromatin interaction
ENSG00000151881	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10036954	0.82[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap]
rs10038608	0.96[MEX][hapmap]
rs10042992	0.96[MEX][hapmap]
rs10055801	1.00[CEU][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs10057103	0.96[MEX][hapmap]
rs10058558	0.96[MEX][hapmap]
rs10059912	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10059993	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10061165	0.96[MEX][hapmap]
rs10065863	0.96[MEX][hapmap]
rs10068064	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10074682	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs10462051	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11949083	0.94[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11952832	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11958046	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12187908	0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs12332560	0.86[ASN][1000 genomes]
rs12521249	0.83[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12651879	0.84[ASN][1000 genomes]
rs12652547	0.96[MEX][hapmap]
rs12697457	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13189004	0.96[MEX][hapmap]
rs13189484	0.81[EUR][1000 genomes]
rs13359906	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1366410	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1389868	1.00[JPT][hapmap]
rs1593971	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[JPT][hapmap]
rs2131998	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2172763	0.96[MEX][hapmap]
rs28437972	0.83[ASN][1000 genomes]
rs28606458	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3776423	0.82[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs3806870	1.00[JPT][hapmap];0.91[MEX][hapmap]
rs4072918	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.83[ASN][1000 genomes]
rs4072919	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.87[TSI][hapmap];0.83[ASN][1000 genomes]
rs4073848	0.96[MEX][hapmap]
rs4074777	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs4331909	0.83[ASN][1000 genomes]
rs4367306	0.96[MEX][hapmap]
rs4386738	1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4428418	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4467713	0.90[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[ASN][1000 genomes]
rs4535459	0.83[ASW][hapmap];0.92[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4610465	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs4866752	0.95[MEX][hapmap]
rs4866833	0.82[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[ASN][1000 genomes]
rs4866835	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55667604	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55855322	0.83[ASN][1000 genomes]
rs56008952	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56097465	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59001943	0.83[ASN][1000 genomes]
rs59224335	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60297702	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6451695	0.82[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs6451696	0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs6451697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6451698	0.86[JPT][hapmap];0.87[MEX][hapmap]
rs6451699	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6451705	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap]
rs6451706	0.95[MEX][hapmap]
rs6451712	0.83[ASN][1000 genomes]
rs6451718	0.96[MEX][hapmap]
rs67261887	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67581152	0.85[ASN][1000 genomes]
rs6860493	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6862102	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6866325	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6866802	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6869933	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6870018	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6878770	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs6884661	0.83[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6885679	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs6891363	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6895327	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs6896693	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs6898866	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs750582	0.96[MEX][hapmap]
rs750583	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7703662	0.96[CEU][hapmap]
rs7705166	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7706431	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7708369	0.96[MEX][hapmap]
rs7710628	0.96[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs7713479	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7715782	0.87[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7717636	0.86[ASN][1000 genomes]
rs7718627	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs7732656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7736108	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7736615	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7737793	0.84[EUR][1000 genomes]
rs9885189	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881017	chr5:43444826-43731692	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	222 gene(s)	inside rSNPs	diseases
2	nsv830275	chr5:43469511-43639384	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	220 gene(s)	inside rSNPs	diseases
3	nsv881108	chr5:43527432-43800333	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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	57 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs10065689	NNT	cis	lymphoblastoid	seeQTL
rs10065689	NNT	cis	cerebellum	SCAN
rs10065689	HSD11B1L	trans	cerebellum	SCAN
rs10065689	YY2	trans	cerebellum	SCAN
rs10065689	NNT	Cis_1M	lymphoblastoid	RTeQTL
rs10065689	C5orf34	cis	parietal	SCAN
rs10065689	NNT	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43600800-43604800	Active TSS	Psoas Muscle	Psoas
2	chr5:43600800-43605200	Active TSS	Right Atrium	heart
3	chr5:43601600-43604400	Active TSS	GM12878-XiMat	blood
4	chr5:43601600-43604600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr5:43601800-43604400	Active TSS	Brain Hippocampus Middle	brain
6	chr5:43601800-43604600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:43601800-43604600	Active TSS	Fetal Brain Female	brain
8	chr5:43601800-43604800	Active TSS	Left Ventricle	heart
9	chr5:43602000-43604400	Active TSS	Fetal Heart	heart
10	chr5:43602000-43604600	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr5:43602000-43604600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr5:43602000-43604600	Active TSS	Aorta	Aorta
13	chr5:43602000-43604800	Active TSS	Right Ventricle	heart
14	chr5:43602200-43604400	Active TSS	Placenta Amnion	Placenta Amnion
15	chr5:43602200-43604600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr5:43602200-43604600	Active TSS	Fetal Stomach	stomach
17	chr5:43602400-43604400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr5:43602400-43604400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr5:43602400-43604400	Active TSS	Fetal Lung	lung
20	chr5:43602400-43604400	Active TSS	Ovary	ovary
21	chr5:43602400-43604400	Active TSS	Pancreas	Pancrea
22	chr5:43602400-43604600	Active TSS	H9 Cell Line	embryonic stem cell
23	chr5:43602400-43604600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:43602400-43604600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr5:43602400-43604600	Active TSS	Colonic Mucosa	Colon
26	chr5:43602400-43604800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:43602600-43604400	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr5:43602600-43604400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:43602600-43604400	Active TSS	Brain Substantia Nigra	brain
30	chr5:43602600-43604400	Active TSS	Fetal Kidney	kidney
31	chr5:43602600-43604600	Active TSS	Fetal Intestine Large	intestine
32	chr5:43602600-43604600	Active TSS	Rectal Smooth Muscle	rectum
33	chr5:43602600-43604800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:43602600-43604800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:43602600-43604800	Active TSS	HSMM	muscle
36	chr5:43602800-43604400	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr5:43603400-43604400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr5:43603400-43604400	Flanking Active TSS	HMEC	breast
39	chr5:43603400-43604600	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr5:43603400-43604800	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr5:43603400-43604800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr5:43603400-43604800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:43603400-43605000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr5:43603400-43605000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:43603600-43604400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:43603600-43604400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:43603600-43604400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:43603600-43604400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
49	chr5:43603600-43604400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr5:43603600-43604400	Flanking Active TSS	Placenta	Placenta

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