Variant report

Variant	rs189403002
Chromosome Location	chr5:176923871-176923872
allele	A/G
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	STAT3	chr5:176923749-176923955	MCF10A-Er-Src	breast:	n/a	chr5:176923884-176923896
2	POLR2A	chr5:176923117-176925060	HUVEC	blood vessel:	n/a	n/a
3	RCOR1	chr5:176923841-176924006	HepG2	liver:	n/a	n/a
4	CHD2	chr5:176923375-176925045	Hela-S3	cervix:	n/a	n/a
5	MYC	chr5:176923231-176925039	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr5:176919037-176923987	H1-hESC	embryonic stem cell:	n/a	n/a
7	SRF	chr5:176923772-176924004	K562	blood:	n/a	chr5:176923937-176923948 chr5:176923934-176923952 chr5:176923869-176923879
8	CCNT2	chr5:176923698-176925712	K562	blood:	n/a	chr5:176924645-176924654 chr5:176923889-176923898 chr5:176923731-176923740 chr5:176924814-176924823
9	TAF1	chr5:176923702-176924064	PFSK-1	brain:	n/a	n/a
10	HEY1	chr5:176923724-176924289	HepG2	liver:	n/a	n/a
11	JUND	chr5:176923727-176924215	H1-hESC	embryonic stem cell:	n/a	chr5:176923863-176923871 chr5:176923859-176923870 chr5:176923861-176923872 chr5:176923861-176923873
12	TAF1	chr5:176923828-176923992	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr5:176923561-176924128	HepG2	liver:	n/a	n/a
14	POLR2A	chr5:176923662-176924089	A549	lung:	n/a	n/a
15	POLR2A	chr5:176921609-176925367	ProgFib	skin:	n/a	n/a
16	HEY1	chr5:176920762-176925766	K562	blood:	n/a	chr5:176924290-176924305 chr5:176924354-176924369
17	POLR2A	chr5:176920718-176925182	GM12878	blood:	n/a	n/a
18	CBX3	chr5:176923533-176924044	K562	blood:	n/a	n/a
19	NANOG	chr5:176923639-176923970	H1-hESC	embryonic stem cell:	n/a	n/a
20	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
21	POLR2A	chr5:176923763-176925113	K562	blood:	n/a	n/a
22	MAX	chr5:176923408-176925408	MCF-7	breast:	n/a	n/a
23	MAX	chr5:176923452-176925852	K562	blood:	n/a	n/a
24	POLR2A	chr5:176920925-176925879	K562	blood:	n/a	n/a
25	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
26	UBTF	chr5:176923680-176925824	K562	blood:	n/a	n/a
27	POLR2A	chr5:176923124-176925637	K562	blood:	n/a	n/a
28	SRF	chr5:176923734-176924101	HepG2	liver:	n/a	chr5:176923937-176923948 chr5:176923934-176923952 chr5:176923869-176923879
29	NFIC	chr5:176923235-176924659	ECC-1	luminal epithelium:	n/a	n/a
30	FOSL2	chr5:176923653-176924016	HepG2	liver:	n/a	chr5:176923863-176923871 chr5:176923859-176923870 chr5:176923861-176923872 chr5:176923861-176923873
31	TAF1	chr5:176923572-176925108	K562	blood:	n/a	n/a
32	SRF	chr5:176923687-176924131	H1-hESC	embryonic stem cell:	n/a	chr5:176923937-176923948 chr5:176923934-176923952 chr5:176923869-176923879
33	FOSL1	chr5:176923666-176924086	K562	blood:	n/a	chr5:176923863-176923871 chr5:176923859-176923870 chr5:176923861-176923872 chr5:176923861-176923872 chr5:176923861-176923873
34	GTF2F1	chr5:176923719-176923951	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr5:176923740-176923890	AG04449	skin:	n/a	n/a
36	POLR2A	chr5:176923252-176925132	SK-N-MC	brain:	n/a	n/a
37	MAX	chr5:176922378-176925278	A549	lung:	n/a	n/a
38	CEBPD	chr5:176923409-176925812	K562	blood:	n/a	chr5:176925100-176925111 chr5:176925102-176925111
39	YY1	chr5:176923688-176924004	K562	blood:	n/a	chr5:176923886-176923897 chr5:176923889-176923898
40	MAX	chr5:176923458-176924047	A549	lung:	n/a	n/a
41	POLR2A	chr5:176919522-176925218	H1-hESC	embryonic stem cell:	n/a	n/a
42	ZNF143	chr5:176923843-176925157	H1-hESC	embryonic stem cell:	n/a	chr5:176924440-176924458 chr5:176923894-176923912 chr5:176924869-176924879
43	REST	chr5:176923752-176924049	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr5:176923141-176925077	HepG2	liver:	n/a	n/a
45	ELF1	chr5:176923728-176924034	K562	blood:	n/a	n/a
46	MAX	chr5:176923380-176924177	SK-N-SH	brain:	n/a	n/a
47	TEAD4	chr5:176922430-176925969	K562	blood:	n/a	n/a
48	SIN3A	chr5:176923187-176925425	H1-hESC	embryonic stem cell:	n/a	chr5:176924114-176924128 chr5:176923604-176923617 chr5:176923625-176923638
49	BHLHE40	chr5:176923282-176925787	K562	blood:	n/a	chr5:176924868-176924884 chr5:176924483-176924499 chr5:176924352-176924368 chr5:176924636-176924652
50	TAF1	chr5:176923727-176925068	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:176923028..176926285-chr5:177025596..177029619,3	MCF-7	breast:
2	chr5:176735682..176745085-chr5:176921866..176925758,11	K562	blood:
3	chr5:176827670..176832994-chr5:176921295..176926945,8	MCF-7	breast:
4	chr5:176922387..176924706-chr5:176979914..176982502,2	MCF-7	breast:
5	chr5:176923095..176925209-chr5:177019148..177022259,3	MCF-7	breast:
6	chr5:176728198..176732998-chr5:176923709..176925672,5	K562	blood:
7	chr5:176557961..176562995-chr5:176922824..176926506,4	K562	blood:
8	chr5:176431208..176433685-chr5:176921378..176924111,2	K562	blood:
9	chr3:157827515..157828163-chr5:176923762..176924298,2	Hela-S3	cervix:
10	chr5:176923072..176926532-chr5:176980245..176983139,4	K562	blood:
11	chr5:176923162..176925760-chr5:176965649..176968131,3	K562	blood:
12	chr5:176922579..176925417-chr5:176960443..176963610,5	K562	blood:
13	chr5:176733741..176736131-chr5:176921060..176924841,3	MCF-7	breast:
14	chr5:176922896..176925677-chr5:176978931..176981454,4	MCF-7	breast:
15	chr5:176519593..176521412-chr5:176923505..176925099,2	K562	blood:
16	chr5:176923602..176926182-chr5:177017999..177019710,2	K562	blood:
17	chr5:176814610..176818995-chr5:176923007..176929143,6	MCF-7	breast:
18	chr5:175969631..175971381-chr5:176922685..176924938,2	K562	blood:
19	chr5:176923371..176925329-chr5:177557854..177560543,2	MCF-7	breast:
20	chr5:176922985..176925564-chr5:177025681..177028407,2	MCF-7	breast:
21	chr5:176557706..176561647-chr5:176923126..176925681,5	MCF-7	breast:
22	chr5:176784055..176785705-chr5:176923160..176925577,2	MCF-7	breast:
23	chr5:176923252..176925841-chr5:177025670..177028479,3	K562	blood:
24	chr5:176792723..176794466-chr5:176923269..176925960,2	MCF-7	breast:
25	chr5:176922040..176925610-chr5:177017064..177019499,4	K562	blood:
26	chr5:176736901..176740398-chr5:176920138..176924378,4	MCF-7	breast:
27	chr5:176738003..176740691-chr5:176923157..176926239,4	MCF-7	breast:
28	chr5:176737737..176740536-chr5:176922032..176926292,7	K562	blood:

Variant related genes	Relation type
PDLIM7	TF binding region
ENSG00000131183	Chromatin interaction
ENSG00000074276	Chromatin interaction
ENSG00000131187	Chromatin interaction
ENSG00000174891	Chromatin interaction
ENSG00000213347	Chromatin interaction
ENSG00000165671	Chromatin interaction
ENSG00000198055	Chromatin interaction
ENSG00000169220	Chromatin interaction
ENSG00000087206	Chromatin interaction
ENSG00000184840	Chromatin interaction
ENSG00000169230	Chromatin interaction
ENSG00000027847	Chromatin interaction
ENSG00000146067	Chromatin interaction
ENSG00000160867	Chromatin interaction
ENSG00000272459	Chromatin interaction
ENSG00000145916	Chromatin interaction
ENSG00000169228	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:25 , 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	nsv883176	chr5:176843297-176924175	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:176917800-176924200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr5:176920000-176924000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr5:176920400-176924000	Enhancers	Primary B cells from peripheral blood	blood
4	chr5:176920400-176924000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr5:176920800-176924000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr5:176921600-176924200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:176921800-176924000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr5:176922200-176925400	Active TSS	Aorta	Aorta
9	chr5:176922600-176924000	Enhancers	Primary T cells from cord blood	blood
10	chr5:176922600-176924400	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr5:176922800-176924000	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr5:176922800-176924200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr5:176922800-176924200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr5:176923000-176924000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr5:176923000-176924000	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr5:176923000-176924400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr5:176923000-176924600	Flanking Active TSS	Colonic Mucosa	Colon
18	chr5:176923000-176924800	Active TSS	Brain Hippocampus Middle	brain
19	chr5:176923000-176925000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:176923000-176925200	Active TSS	Brain Angular Gyrus	brain
21	chr5:176923000-176925200	Active TSS	Left Ventricle	heart
22	chr5:176923000-176925600	Active TSS	Brain Anterior Caudate	brain
23	chr5:176923200-176924000	Flanking Active TSS	Spleen	Spleen
24	chr5:176923200-176925000	Active TSS	Gastric	stomach
25	chr5:176923200-176925000	Active TSS	A549	lung
26	chr5:176923200-176925000	Active TSS	NHDF-Ad	bronchial
27	chr5:176923200-176925200	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr5:176923200-176925200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:176923200-176925600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr5:176923200-176925600	Active TSS	H9 Cell Line	embryonic stem cell
31	chr5:176923200-176925600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr5:176923200-176925600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:176923400-176924000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr5:176923400-176924200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr5:176923400-176924200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr5:176923400-176924400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:176923400-176924800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:176923400-176924800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr5:176923400-176925000	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr5:176923400-176925000	Active TSS	NH-A	brain
41	chr5:176923400-176925200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:176923400-176925200	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr5:176923400-176925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:176923400-176925200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:176923400-176925200	Active TSS	Rectal Smooth Muscle	rectum
46	chr5:176923400-176925400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:176923400-176925400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:176923400-176925400	Flanking Active TSS	Dnd41	blood
49	chr5:176923400-176925600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:176923400-176925600	Active TSS	Fetal Kidney	kidney

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