Variant report

Variant	rs552800488
Chromosome Location	chr5:176924689-176924690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:176923117-176925060	HUVEC	blood vessel:	n/a	n/a
2	USF2	chr5:176924550-176924925	GM12878	blood:	n/a	chr5:176924868-176924884 chr5:176924636-176924652
3	BHLHE40	chr5:176924218-176924859	GM12878	blood:	n/a	chr5:176924483-176924499 chr5:176924352-176924368 chr5:176924636-176924652
4	RCOR1	chr5:176924054-176925962	K562	blood:	n/a	n/a
5	FOXM1	chr5:176924209-176924692	GM12878	blood:	n/a	n/a
6	CHD2	chr5:176923375-176925045	Hela-S3	cervix:	n/a	n/a
7	E2F6	chr5:176924383-176925181	A549	lung:	n/a	chr5:176924472-176924482 chr5:176924645-176924654
8	MYC	chr5:176923231-176925039	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr5:176924311-176924733	SK-N-SH	brain:	n/a	n/a
10	CREB1	chr5:176924289-176925017	GM12878	blood:	n/a	n/a
11	CCNT2	chr5:176923698-176925712	K562	blood:	n/a	chr5:176924645-176924654 chr5:176923889-176923898 chr5:176923731-176923740 chr5:176924814-176924823
12	POLR2A	chr5:176923886-176925076	GM15510	blood:	n/a	n/a
13	HEY1	chr5:176924294-176925083	HepG2	liver:	n/a	chr5:176924354-176924369
14	TCF12	chr5:176924332-176924745	GM12878	blood:	n/a	chr5:176924651-176924661
15	POLR2A	chr5:176923900-176925039	GM10847	blood:	n/a	n/a
16	PAX5	chr5:176924436-176924738	GM12878	blood:	n/a	n/a
17	TBL1XR1	chr5:176924325-176924990	GM12878	blood:	n/a	n/a
18	CUX1	chr5:176924556-176924702	K562	blood:	n/a	n/a
19	POLR2A	chr5:176924025-176925032	GM12878	blood:	n/a	n/a
20	POLR2A	chr5:176921609-176925367	ProgFib	skin:	n/a	n/a
21	HEY1	chr5:176920762-176925766	K562	blood:	n/a	chr5:176924290-176924305 chr5:176924354-176924369
22	POLR2A	chr5:176920718-176925182	GM12878	blood:	n/a	n/a
23	TBP	chr5:176924399-176925026	GM12878	blood:	n/a	n/a
24	NANOG	chr5:176924408-176925102	H1-hESC	embryonic stem cell:	n/a	chr5:176924467-176924476
25	FOXP2	chr5:176924432-176924772	SK-N-MC	brain:	n/a	n/a
26	JUN	chr5:176920923-176925966	K562	blood:	n/a	chr5:176921780-176921792 chr5:176921781-176921791 chr5:176923863-176923871 chr5:176923859-176923870 chr5:176921782-176921790 chr5:176923861-176923872 chr5:176921566-176921575 chr5:176924269-176924277 chr5:176924268-176924278 chr5:176923861-176923873
27	ELK1	chr5:176924686-176924971	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr5:176923763-176925113	K562	blood:	n/a	n/a
29	MAX	chr5:176923408-176925408	MCF-7	breast:	n/a	n/a
30	ELF1	chr5:176924110-176925028	K562	blood:	n/a	chr5:176924354-176924366 chr5:176924320-176924332
31	TAF1	chr5:176924407-176924750	GM12892	blood:	n/a	n/a
32	MAX	chr5:176923452-176925852	K562	blood:	n/a	n/a
33	IRF1	chr5:176924415-176925103	K562	blood:	n/a	chr5:176924644-176924658 chr5:176924658-176924672 chr5:176924675-176924689
34	CREB1	chr5:176924153-176925529	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr5:176920925-176925879	K562	blood:	n/a	n/a
36	JUND	chr5:176923461-176925105	MCF-7	breast:	n/a	chr5:176923863-176923871 chr5:176923859-176923870 chr5:176923861-176923872 chr5:176924269-176924277 chr5:176924268-176924278 chr5:176923861-176923873
37	UBTF	chr5:176923680-176925824	K562	blood:	n/a	n/a
38	TCF7L2	chr5:176924656-176925148	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr5:176924109-176925090	GM12891	blood:	n/a	n/a
40	POLR2A	chr5:176923124-176925637	K562	blood:	n/a	n/a
41	E2F4	chr5:176924187-176924980	MCF10A-Er-Src	breast:	n/a	chr5:176924472-176924482 chr5:176924338-176924347 chr5:176924645-176924654
42	POLR2A	chr5:176923939-176925094	GM12878	blood:	n/a	n/a
43	ELF1	chr5:176924241-176925153	GM12878	blood:	n/a	chr5:176924354-176924366 chr5:176924320-176924332
44	TAF1	chr5:176923572-176925108	K562	blood:	n/a	n/a
45	EP300	chr5:176924440-176924940	GM12878	blood:	n/a	n/a
46	REST	chr5:176924419-176924693	HepG2	liver:	n/a	n/a
47	POLR2A	chr5:176923252-176925132	SK-N-MC	brain:	n/a	n/a
48	MAX	chr5:176922378-176925278	A549	lung:	n/a	n/a
49	E2F6	chr5:176924361-176924723	K562	blood:	n/a	chr5:176924472-176924482 chr5:176924645-176924654
50	CEBPD	chr5:176923409-176925812	K562	blood:	n/a	chr5:176925100-176925111 chr5:176925102-176925111

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:176924682-176924732	HRPEpiC	eye:	n/a
2	chr5:176924682-176924732	NB4	blood:	n/a
3	chr5:176924674-176924724	SK-N-SH_RA	brain:	n/a
4	chr5:176924682-176924732	HNPCEpiC	eye:	n/a
5	chr5:176924674-176924724	HL-60	blood:	n/a
6	chr5:176924674-176924724	AG10803	skin:	n/a
7	chr5:176924682-176924732	NHDF-neo	bronchial:	n/a
8	chr5:176924682-176924732	AoSMC	blood vessel:	n/a
9	chr5:176924682-176924732	MCF10A-Er-Src	breast:	n/a
10	chr5:176924682-176924732	HL-60	blood:	n/a
11	chr5:176924674-176924724	IMR90	lung:	fetal
12	chr5:176924682-176924732	GM19239	blood:	n/a
13	chr5:176924674-176924724	HUVEC	blood vessel:	n/a
14	chr5:176924682-176924732	GM12892	blood:	n/a
15	chr5:176924674-176924724	H1-hESC	embryonic stem cell:	embryo
16	chr5:176924682-176924732	HCPEpiC	choroid plexus:	n/a
17	chr5:176924674-176924724	HRPEpiC	eye:	n/a
18	chr5:176924682-176924732	HepG2	liver:	n/a
19	chr5:176924682-176924732	HEEpiC	esophagus:	n/a
20	chr5:176924682-176924732	K562	blood:	n/a
21	chr5:176924682-176924732	Hela-S3	cervix:	n/a
22	chr5:176924682-176924732	HCF	heart:	n/a
23	chr5:176924674-176924724	ovcar-3	ovarian:	n/a
24	chr5:176924674-176924724	HCM	heart:	n/a
25	chr5:176924674-176924724	GM12892	blood:	n/a
26	chr5:176924674-176924724	PFSK-1	brain:	n/a
27	chr5:176924674-176924724	Jurkat	blood:	n/a
28	chr5:176924674-176924724	RPTEC	kidney:	n/a
29	chr5:176924674-176924724	HepG2	liver:	n/a
30	chr5:176924682-176924732	HEK293	kidney:	embryo
31	chr5:176924674-176924724	MCF-7	breast:	n/a
32	chr5:176924682-176924732	SKMC	muscle:	n/a
33	chr5:176924674-176924724	HCF	heart:	n/a
34	chr5:176924674-176924724	GM19239	blood:	n/a
35	chr5:176924674-176924724	AG09319	gingival:	n/a
36	chr5:176924674-176924724	NH-A	brain:	n/a
37	chr5:176924682-176924732	A549	lung:	n/a
38	chr5:176924682-176924732	T-47D	breast:	n/a
39	chr5:176924674-176924724	PrEC	prostate:	n/a
40	chr5:176924674-176924724	HCPEpiC	choroid plexus:	n/a
41	chr5:176924674-176924724	K562	blood:	n/a
42	chr5:176924682-176924732	RPTEC	kidney:	n/a
43	chr5:176924674-176924724	ProgFib	skin:	n/a
44	chr5:176924674-176924724	SKMC	muscle:	n/a
45	chr5:176924682-176924732	HMEC	breast:	n/a
46	chr5:176924682-176924732	Hepatocyte	liver:	n/a
47	chr5:176924682-176924732	AG09309	skin:	n/a
48	chr5:176924682-176924732	IMR90	lung:	fetal
49	chr5:176924674-176924724	CMK	blood:	n/a
50	chr5:176924682-176924732	ECC-1	luminal epithelium:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:62222989..62223603-chr5:176924432..176925193,2	HCT-116	colon:
2	chr5:176923028..176926285-chr5:177025596..177029619,3	MCF-7	breast:
3	chr14:39901309..39901883-chr5:176924137..176924694,2	Hela-S3	cervix:
4	chr5:176735682..176745085-chr5:176921866..176925758,11	K562	blood:
5	chr5:176827670..176832994-chr5:176921295..176926945,8	MCF-7	breast:
6	chr5:176922387..176924706-chr5:176979914..176982502,2	MCF-7	breast:
7	chr5:176923095..176925209-chr5:177019148..177022259,3	MCF-7	breast:
8	chr20:54966730..54967370-chr5:176924121..176925044,2	Hela-S3	cervix:
9	chr17:56735906..56737887-chr5:176924171..176926025,2	MCF-7	breast:
10	chr5:176728198..176732998-chr5:176923709..176925672,5	K562	blood:
11	chr5:176557961..176562995-chr5:176922824..176926506,4	K562	blood:
12	chr5:176923072..176926532-chr5:176980245..176983139,4	K562	blood:
13	chr5:176923162..176925760-chr5:176965649..176968131,3	K562	blood:
14	chr5:176922579..176925417-chr5:176960443..176963610,5	K562	blood:
15	chr5:176924088..176925048-chr8:125486448..125487055,2	Hela-S3	cervix:
16	chr5:176733741..176736131-chr5:176921060..176924841,3	MCF-7	breast:
17	chr19:39926030..39926817-chr5:176924186..176924945,2	Hela-S3	cervix:
18	chr5:176922896..176925677-chr5:176978931..176981454,4	MCF-7	breast:
19	chr1:180123549..180124057-chr5:176924083..176924757,2	Hela-S3	cervix:
20	chr5:176519593..176521412-chr5:176923505..176925099,2	K562	blood:
21	chr20:442837..443546-chr5:176924358..176925028,2	HCT-116	colon:
22	chr5:176923602..176926182-chr5:177017999..177019710,2	K562	blood:
23	chr5:176814610..176818995-chr5:176923007..176929143,6	MCF-7	breast:
24	chr5:175969631..175971381-chr5:176922685..176924938,2	K562	blood:
25	chr5:176923371..176925329-chr5:177557854..177560543,2	MCF-7	breast:
26	chr5:176922985..176925564-chr5:177025681..177028407,2	MCF-7	breast:
27	chr5:176557706..176561647-chr5:176923126..176925681,5	MCF-7	breast:
28	chr5:176784055..176785705-chr5:176923160..176925577,2	MCF-7	breast:
29	chr5:176923252..176925841-chr5:177025670..177028479,3	K562	blood:
30	chr5:176792723..176794466-chr5:176923269..176925960,2	MCF-7	breast:
31	chr17:73775369..73776233-chr5:176924198..176925025,2	Hela-S3	cervix:
32	chr5:176922040..176925610-chr5:177017064..177019499,4	K562	blood:
33	chr5:70882556..70884981-chr5:176924076..176925754,2	MCF-7	breast:
34	chr5:176738003..176740691-chr5:176923157..176926239,4	MCF-7	breast:
35	chr5:176737737..176740536-chr5:176922032..176926292,7	K562	blood:

No data

Variant related genes	Relation type
PDLIM7	TF binding region
PDLIM7	CpG island
ENSG00000165671	Chromatin interaction
ENSG00000169228	Chromatin interaction
ENSG00000131187	Chromatin interaction
ENSG00000213347	Chromatin interaction
ENSG00000272459	Chromatin interaction
ENSG00000266402	Chromatin interaction
ENSG00000027847	Chromatin interaction
ENSG00000170881	Chromatin interaction
ENSG00000105193	Chromatin interaction
ENSG00000184840	Chromatin interaction
ENSG00000145916	Chromatin interaction
ENSG00000199753	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000146067	Chromatin interaction
ENSG00000087586	Chromatin interaction
ENSG00000169220	Chromatin interaction
ENSG00000131844	Chromatin interaction
ENSG00000196235	Chromatin interaction
ENSG00000165355	Chromatin interaction
ENSG00000116260	Chromatin interaction
ENSG00000169230	Chromatin interaction
ENSG00000131183	Chromatin interaction
ENSG00000074276	Chromatin interaction
ENSG00000160867	Chromatin interaction
ENSG00000198055	Chromatin interaction
ENSG00000125875	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000245149	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916108	chr5:176688459-177078723	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
2	nsv883158	chr5:176726635-176931706	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
3	nsv883160	chr5:176740996-176952919	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS 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	116 gene(s)	inside rSNPs	diseases
4	nsv1024444	chr5:176751921-177427715	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
5	nsv883161	chr5:176754722-176958397	Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	nsv1020334	chr5:176779108-176954933	Weak transcription Enhancers Strong transcription Flanking Active TSS 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 target site	114 gene(s)	inside rSNPs	diseases
7	nsv883164	chr5:176780545-177003616	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
8	esv1816147	chr5:176787037-176966509	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv883166	chr5:176817636-176940384	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers 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 target site	108 gene(s)	inside rSNPs	diseases
10	nsv883170	chr5:176824137-176952919	Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv883173	chr5:176842474-176931706	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
12	nsv883174	chr5:176842474-176940384	Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
13	nsv883175	chr5:176842474-176952919	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
14	nsv1030965	chr5:176851182-176937654	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
15	nsv1026103	chr5:176851182-176942552	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
16	nsv1022832	chr5:176861503-176937654	Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
17	nsv1018088	chr5:176861503-176942552	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
18	nsv1028123	chr5:176861503-176949149	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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 target site	83 gene(s)	inside rSNPs	diseases
19	nsv537965	chr5:176861503-176949149	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
20	nsv883177	chr5:176868358-177003616	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS 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	84 gene(s)	inside rSNPs	diseases
21	esv2752795	chr5:176898619-177488281	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
22	nsv883179	chr5:176912073-176926674	Genic enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking 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	40 gene(s)	inside rSNPs	diseases
23	nsv883180	chr5:176912073-176937177	Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS 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	42 gene(s)	inside rSNPs	diseases
24	nsv984570	chr5:176923414-176956300	Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:176922200-176925400	Active TSS	Aorta	Aorta
2	chr5:176923000-176924800	Active TSS	Brain Hippocampus Middle	brain
3	chr5:176923000-176925000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:176923000-176925200	Active TSS	Brain Angular Gyrus	brain
5	chr5:176923000-176925200	Active TSS	Left Ventricle	heart
6	chr5:176923000-176925600	Active TSS	Brain Anterior Caudate	brain
7	chr5:176923200-176925000	Active TSS	Gastric	stomach
8	chr5:176923200-176925000	Active TSS	A549	lung
9	chr5:176923200-176925000	Active TSS	NHDF-Ad	bronchial
10	chr5:176923200-176925200	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr5:176923200-176925200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:176923200-176925600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr5:176923200-176925600	Active TSS	H9 Cell Line	embryonic stem cell
14	chr5:176923200-176925600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr5:176923200-176925600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr5:176923400-176924800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:176923400-176924800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr5:176923400-176925000	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr5:176923400-176925000	Active TSS	NH-A	brain
20	chr5:176923400-176925200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:176923400-176925200	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr5:176923400-176925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:176923400-176925200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:176923400-176925200	Active TSS	Rectal Smooth Muscle	rectum
25	chr5:176923400-176925400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr5:176923400-176925400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:176923400-176925400	Flanking Active TSS	Dnd41	blood
28	chr5:176923400-176925600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:176923400-176925600	Active TSS	Fetal Kidney	kidney
30	chr5:176923600-176924800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:176923600-176924800	Active TSS	Brain Substantia Nigra	brain
32	chr5:176923600-176924800	Active TSS	Fetal Lung	lung
33	chr5:176923600-176924800	Active TSS	Right Ventricle	heart
34	chr5:176923600-176924800	Active TSS	Thymus	Thymus
35	chr5:176923600-176925000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:176923600-176925000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:176923600-176925000	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr5:176923600-176925000	Active TSS	GM12878-XiMat	blood
39	chr5:176923600-176925000	Active TSS	HepG2	liver
40	chr5:176923600-176925000	Active TSS	Osteobl	bone
41	chr5:176923600-176925200	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr5:176923600-176925200	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr5:176923600-176925200	Active TSS	Psoas Muscle	Psoas
44	chr5:176923600-176925600	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr5:176923600-176925600	Active TSS	Colon Smooth Muscle	Colon
46	chr5:176923600-176925800	Active TSS	HSMM	muscle
47	chr5:176923800-176924800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:176923800-176924800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:176923800-176924800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:176923800-176924800	Active TSS	Primary neutrophils fromperipheralblood	blood

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