Variant report

Variant	rs972890
Chromosome Location	chr5:1800436-1800437
allele	A/C
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	JUND	chr5:1799770-1802111	K562	blood:	n/a	chr5:1799990-1799999 chr5:1799987-1799996 chr5:1800154-1800168 chr5:1799991-1800000 chr5:1799988-1799997
2	RCOR1	chr5:1799791-1801796	Hela-S3	cervix:	n/a	n/a
3	CREB1	chr5:1799683-1800675	K562	blood:	n/a	n/a
4	SMARCC2	chr5:1799899-1801839	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr5:1800409-1800661	K562	blood:	n/a	n/a
6	MBD4	chr5:1799988-1800649	HepG2	liver:	n/a	n/a
7	TBP	chr5:1799280-1802309	K562	blood:	n/a	n/a
8	CREB1	chr5:1799647-1800492	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr5:1799337-1802213	K562	blood:	n/a	n/a
10	POLR2A	chr5:1799035-1800569	GM12891	blood:	n/a	n/a
11	POLR2A	chr5:1799154-1802375	MCF10A-Er-Src	breast:	n/a	n/a
12	MAX	chr5:1799413-1801875	HepG2	liver:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
13	HA-E2F1	chr5:1799960-1802245	MCF-7	breast:	n/a	chr5:1801422-1801431 chr5:1801419-1801431 chr5:1801475-1801484 chr5:1800052-1800061 chr5:1801454-1801461 chr5:1801453-1801462 chr5:1799984-1799993
14	CCNT2	chr5:1799531-1800899	K562	blood:	n/a	chr5:1799739-1799748
15	ZKSCAN1	chr5:1799624-1800896	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr5:1799337-1802013	GM12878	blood:	n/a	chr5:1801420-1801430
17	POLR2A	chr5:1799365-1800786	K562	blood:	n/a	n/a
18	FOXA1	chr5:1800147-1800442	ECC-1	luminal epithelium:	n/a	chr5:1800282-1800297
19	POLR2A	chr5:1800416-1800632	A549	lung:	n/a	n/a
20	CTCF	chr5:1799945-1800701	GM12878	blood:	n/a	n/a
21	EP300	chr5:1799793-1800437	GM12878	blood:	n/a	chr5:1800073-1800086 chr5:1800283-1800293
22	SMARCC1	chr5:1800159-1802268	Hela-S3	cervix:	n/a	n/a
23	TBP	chr5:1799787-1802268	H1-hESC	embryonic stem cell:	n/a	n/a
24	RCOR1	chr5:1799815-1800927	K562	blood:	n/a	n/a
25	POLR2A	chr5:1799089-1802204	HepG2	liver:	n/a	n/a
26	POLR2A	chr5:1799582-1801049	ECC-1	luminal epithelium:	n/a	n/a
27	TEAD4	chr5:1799783-1801813	K562	blood:	n/a	n/a
28	POLR2A	chr5:1799155-1802340	Hela-S3	cervix:	n/a	n/a
29	FOXA2	chr5:1799968-1800440	HepG2	liver:	n/a	n/a
30	POLR2A	chr5:1798976-1802439	Hela-S3	cervix:	n/a	n/a
31	SIN3AK20	chr5:1800337-1800950	K562	blood:	n/a	n/a
32	TFAP2C	chr5:1799840-1802225	Hela-S3	cervix:	n/a	n/a
33	SMARCB1	chr5:1799152-1800762	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr5:1800416-1800656	HepG2	liver:	n/a	n/a
35	POLR2A	chr5:1800367-1801848	PFSK-1	brain:	n/a	n/a
36	FOXA1	chr5:1800014-1800445	HepG2	liver:	n/a	chr5:1800282-1800297
37	CHD1	chr5:1800125-1800813	H1-hESC	embryonic stem cell:	n/a	n/a
38	SMC3	chr5:1799868-1801925	Hela-S3	cervix:	n/a	chr5:1801716-1801723 chr5:1801424-1801434
39	CEBPB	chr5:1799929-1800470	GM12878	blood:	n/a	n/a
40	IRF1	chr5:1799536-1802910	K562	blood:	n/a	chr5:1799833-1799847 chr5:1800183-1800196 chr5:1801111-1801131 chr5:1801418-1801432
41	TEAD4	chr5:1799934-1800605	K562	blood:	n/a	n/a
42	RUNX3	chr5:1799602-1801810	GM12878	blood:	n/a	n/a
43	TBP	chr5:1799852-1800791	HepG2	liver:	n/a	n/a
44	POLR2A	chr5:1799292-1800719	GM12878	blood:	n/a	n/a
45	ELK1	chr5:1799837-1801828	Hela-S3	cervix:	n/a	n/a
46	MXI1	chr5:1799161-1802292	Hela-S3	cervix:	n/a	chr5:1800777-1800786 chr5:1799999-1800008 chr5:1800586-1800595
47	POLR2A	chr5:1799722-1801894	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr5:1800394-1800769	GM12878	blood:	n/a	n/a
49	CTCF	chr5:1800340-1800490	NHDF-neo	bronchial:	n/a	n/a
50	FOXA2	chr5:1799855-1800605	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:56707453..56709236-chr5:1799018..1801500,2	MCF-7	breast:
2	chr5:1799841..1802509-chr5:1881368..1882987,2	K562	blood:
3	chr5:1799569..1802884-chr5:1886598..1889173,4	MCF-7	breast:
4	chr5:1799911..1800807-chr9:106856184..106857050,2	Hela-S3	cervix:
5	chr17:73716503..73719364-chr5:1799934..1802626,2	MCF-7	breast:
6	chr12:120728613..120731132-chr5:1800155..1802952,2	MCF-7	breast:
7	chr5:1793765..1806799-chr5:1879445..1889322,45	MCF-7	breast:
8	chr5:1344287..1345865-chr5:1799704..1802609,2	K562	blood:
9	chr5:1796457..1805482-chr5:1878036..1885786,21	MCF-7	breast:
10	chr15:93351650..93352450-chr5:1800175..1800757,2	Hela-S3	cervix:
11	chr5:1343974..1345787-chr5:1800029..1802609,2	K562	blood:
12	chr5:1798942..1801341-chr5:1879541..1882987,3	K562	blood:
13	chr2:197791233..197791932-chr5:1799906..1800564,2	HCT-116	colon:
14	chr16:30388347..30389291-chr5:1800052..1800675,2	Hela-S3	cervix:
15	chr20:47894959..47895488-chr5:1800047..1800851,2	Hela-S3	cervix:
16	chr5:1799532..1800526-chrX:15693324..15693931,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFS6-9	chr5:1799992-1801417	NONHSAT100069

Variant related genes	Relation type
NDUFS6	TF binding region
MRPL36	TF binding region
ENSG00000186312	Chromatin interaction
ENSG00000180209	Chromatin interaction
ENSG00000049656	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000113430	Chromatin interaction
ENSG00000258922	Chromatin interaction
ENSG00000200795	Chromatin interaction
ENSG00000249116	Chromatin interaction
ENSG00000249326	Chromatin interaction
ENSG00000124201	Chromatin interaction
ENSG00000136824	Chromatin interaction
ENSG00000177410	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000209042	Chromatin interaction
ENSG00000132470	Chromatin interaction
ENSG00000197121	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11133910	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11133911	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11133912	0.94[ASN][1000 genomes]
rs13187162	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1845288	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1873926	1.00[ASW][hapmap];0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2242412	0.89[ASN][1000 genomes]
rs2276986	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2291944	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs34233926	0.96[ASN][1000 genomes]
rs35380881	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3752844	0.83[YRI][hapmap]
rs3756343	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3756345	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3756346	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3776141	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3776142	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3776143	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3776144	0.95[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs3776145	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3776146	0.96[ASN][1000 genomes]
rs3776149	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822364	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4147769	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147770	0.99[ASN][1000 genomes]
rs4147772	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147773	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4975845	0.81[CHB][hapmap];0.89[CHD][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs4975847	0.84[JPT][hapmap]
rs4975848	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4975849	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4975851	0.89[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4975852	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4975853	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55883912	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6555012	0.90[ASN][1000 genomes]
rs6863367	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7702843	0.95[CHB][hapmap];0.91[CHD][hapmap];0.85[JPT][hapmap];0.94[ASN][1000 genomes]
rs972891	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs972892	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs974722	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933805	chr5:1450724-1941619	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
3	nsv1034552	chr5:1658338-1856553	Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
4	nsv537606	chr5:1658338-1856553	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
5	nsv1033147	chr5:1717303-1815821	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers 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	38 gene(s)	inside rSNPs	diseases
6	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
7	nsv1020703	chr5:1724199-1814288	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
8	nsv537608	chr5:1724199-1814288	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv1024133	chr5:1736691-1826510	Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv537609	chr5:1736691-1826510	Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs972890	MRPL36	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1798400-1802400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:1798800-1800600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:1798800-1800600	Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr5:1798800-1802200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:1798800-1802400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr5:1798800-1802800	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr5:1799000-1802200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:1799000-1802200	Active TSS	Left Ventricle	heart
9	chr5:1799000-1802400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:1799000-1802400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr5:1799000-1802400	Active TSS	Psoas Muscle	Psoas
12	chr5:1799000-1802600	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr5:1799000-1802600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr5:1799000-1802600	Active TSS	Fetal Intestine Small	intestine
15	chr5:1799000-1802600	Active TSS	A549	lung
16	chr5:1799200-1800600	Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr5:1799200-1800600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:1799200-1800600	Active TSS	Fetal Intestine Large	intestine
19	chr5:1799200-1800600	Active TSS	HSMM	muscle
20	chr5:1799200-1800800	Active TSS	K562	blood
21	chr5:1799200-1801400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:1799200-1802200	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr5:1799200-1802200	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr5:1799200-1802200	Active TSS	Aorta	Aorta
25	chr5:1799200-1802200	Active TSS	Fetal Kidney	kidney
26	chr5:1799200-1802200	Active TSS	Sigmoid Colon	Sigmoid Colon
27	chr5:1799200-1802200	Active TSS	Small Intestine	intestine
28	chr5:1799200-1802200	Active TSS	NHDF-Ad	bronchial
29	chr5:1799200-1802400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:1799200-1802600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:1799200-1802600	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr5:1799200-1802800	Active TSS	GM12878-XiMat	blood
33	chr5:1799400-1800600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:1799400-1800600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:1799400-1800600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr5:1799400-1800600	Active TSS	Brain Cingulate Gyrus	brain
37	chr5:1799400-1800600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr5:1799400-1800600	Active TSS	Fetal Stomach	stomach
39	chr5:1799400-1800600	Active TSS	Hela-S3	cervix
40	chr5:1799400-1800800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:1799400-1800800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr5:1799400-1800800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:1799400-1800800	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr5:1799400-1800800	Active TSS	Fetal Thymus	thymus
45	chr5:1799400-1800800	Active TSS	Pancreas	Pancrea
46	chr5:1799400-1800800	Active TSS	Placenta Amnion	Placenta Amnion
47	chr5:1799400-1800800	Active TSS	Osteobl	bone
48	chr5:1799400-1801400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr5:1799400-1801800	Active TSS	Fetal Brain Female	brain
50	chr5:1799400-1802000	Active TSS	Primary T killer naive cells fromperipheralblood	blood

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