Variant report

Variant	rs11547064
Chromosome Location	chr5:179228893-179228894
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:179228858-179229201	K562	blood:	n/a	n/a
2	PAX5	chr5:179228780-179229121	GM12878	blood:	n/a	n/a
3	POLR2A	chr5:179228753-179229087	A549	lung:	n/a	n/a
4	IRF4	chr5:179228767-179229177	GM12878	blood:	n/a	n/a
5	POLR2A	chr5:179228800-179231391	K562	blood:	n/a	n/a
6	YY1	chr5:179228799-179229170	GM12878	blood:	n/a	n/a
7	RUNX3	chr5:179228851-179229123	GM12878	blood:	n/a	n/a
8	RAD21	chr5:179228752-179229209	HepG2	liver:	n/a	n/a
9	MAX	chr5:179228770-179229232	A549	lung:	n/a	n/a
10	MAX	chr5:179228713-179229168	H1-hESC	embryonic stem cell:	n/a	n/a
11	SMC3	chr5:179228867-179229234	HepG2	liver:	n/a	n/a
12	POLR2A	chr5:179228149-179229233	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:179228841-179229104	HepG2	liver:	n/a	n/a
14	CTCF	chr5:179228893-179229074	MCF-7	breast:	n/a	n/a
15	RAD21	chr5:179228820-179229205	A549	lung:	n/a	n/a
16	RAD21	chr5:179228851-179229341	SK-N-SH	brain:	n/a	n/a
17	POLR2A	chr5:179228764-179229233	GM12892	blood:	n/a	n/a
18	CTCF	chr5:179228857-179229291	K562	blood:	n/a	chr5:179229196-179229205
19	CTCF	chr5:179228828-179229142	GM19240	blood:	n/a	n/a
20	CTCF	chr5:179228865-179229107	Pancreas_OC	pancreas:	n/a	n/a
21	USF1	chr5:179228844-179229231	H1-hESC	embryonic stem cell:	n/a	n/a
22	ELF1	chr5:179228753-179229118	GM12878	blood:	n/a	n/a
23	POLR2A	chr5:179228692-179229348	PANC-1	pancreas:	n/a	n/a
24	SMC3	chr5:179228750-179229589	SK-N-SH	brain:	n/a	n/a
25	CTCF	chr5:179228642-179229262	HCT-116	colon:	n/a	chr5:179229196-179229205
26	RAD21	chr5:179228727-179229427	HCT-116	colon:	n/a	chr5:179229358-179229372
27	POLR2A	chr5:179228870-179229192	HCT-116	colon:	n/a	n/a
28	MTA3	chr5:179228784-179229339	GM12878	blood:	n/a	n/a
29	POLR2A	chr5:179228636-179229280	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr5:179228182-179229253	GM12878	blood:	n/a	n/a
31	CTCF	chr5:179228860-179229010	NB4	blood:	n/a	n/a
32	CTCF	chr5:179228405-179229422	A549	lung:	n/a	chr5:179229354-179229367 chr5:179229196-179229205
33	EP300	chr5:179228871-179229147	GM12878	blood:	n/a	n/a
34	POLR2A	chr5:179224667-179233676	HL-60	blood:	n/a	n/a
35	CTCF	chr5:179228746-179229205	H1-hESC	embryonic stem cell:	n/a	chr5:179229196-179229205
36	POLR2A	chr5:179228739-179229166	GM12892	blood:	n/a	n/a
37	POLR2A	chr5:179228777-179229045	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr5:179227663-179229654	PANC-1	pancreas:	n/a	n/a
39	CTCF	chr5:179228868-179229122	GM13977	blood:	n/a	n/a
40	CTCF	chr5:179228860-179229010	AG09309	skin:	n/a	n/a
41	NFATC1	chr5:179228736-179229123	GM12878	blood:	n/a	n/a
42	CTCF	chr5:179228842-179229135	NHEK	skin:	n/a	n/a
43	POLR2A	chr5:179228765-179229433	GM12891	blood:	n/a	n/a
44	NANOG	chr5:179228753-179229094	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr5:179228118-179229843	HL-60	blood:	n/a	n/a
46	USF1	chr5:179228868-179229246	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:179228842-179229128	A549	lung:	n/a	n/a
48	PBX3	chr5:179228753-179229150	A549	lung:	n/a	n/a
49	POLR2A	chr5:179228874-179229111	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr5:179228779-179229232	GM12878	blood:	n/a	chr5:179229196-179229205

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179228859-179228909	Hepatocyte	liver:	n/a
2	chr5:179228859-179228909	GM06990	blood:	n/a
3	chr5:179228859-179228909	NHDF-neo	bronchial:	n/a
4	chr5:179228859-179228909	AG04449	skin:	fetal
5	chr5:179228859-179228909	ovcar-3	ovarian:	n/a
6	chr5:179228859-179228909	GM12891	blood:	n/a
7	chr5:179228859-179228909	HCF	heart:	n/a
8	chr5:179228859-179228909	NH-A	brain:	n/a
9	chr5:179228859-179228909	NT2-D1	testis:	n/a
10	chr5:179228859-179228909	Caco-2	colon:	n/a
11	chr5:179228859-179228909	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:179228859-179228909	ECC-1	luminal epithelium:	n/a
13	chr5:179228859-179228909	GM12878	blood:	n/a
14	chr5:179228859-179228909	U87	brain:	n/a
15	chr5:179228859-179228909	HEEpiC	esophagus:	n/a
16	chr5:179228859-179228909	HCM	heart:	n/a
17	chr5:179228859-179228909	HUVEC	blood vessel:	n/a
18	chr5:179228859-179228909	GM12892	blood:	n/a
19	chr5:179228859-179228909	HRCEpiC	kidney:	n/a
20	chr5:179228859-179228909	Hela-S3	cervix:	n/a
21	chr5:179228859-179228909	PFSK-1	brain:	n/a
22	chr5:179228859-179228909	IMR90	lung:	fetal
23	chr5:179228859-179228909	AG09309	skin:	n/a
24	chr5:179228859-179228909	RPTEC	kidney:	n/a
25	chr5:179228859-179228909	BE2_C	brain:	n/a
26	chr5:179228859-179228909	HNPCEpiC	eye:	n/a
27	chr5:179228859-179228909	H1-hESC	embryonic stem cell:	embryo
28	chr5:179228859-179228909	LNCaP	prostate:	n/a
29	chr5:179228859-179228909	HAEpiC	amniotic membrane:	n/a
30	chr5:179228859-179228909	AG10803	skin:	n/a
31	chr5:179228859-179228909	Jurkat	blood:	n/a
32	chr5:179228859-179228909	HCPEpiC	choroid plexus:	n/a
33	chr5:179228859-179228909	HepG2	liver:	n/a
34	chr5:179228859-179228909	BJ	skin:	n/a
35	chr5:179228859-179228909	HL-60	blood:	n/a
36	chr5:179228859-179228909	HCT-116	colon:	n/a
37	chr5:179228859-179228909	SKMC	muscle:	n/a
38	chr5:179228859-179228909	AoSMC	blood vessel:	n/a
39	chr5:179228859-179228909	SAEC	small airway:	n/a
40	chr5:179228859-179228909	HMEC	breast:	n/a
41	chr5:179228859-179228909	HRPEpiC	eye:	n/a
42	chr5:179228859-179228909	HRE	kidney:	n/a
43	chr5:179228859-179228909	K562	blood:	n/a
44	chr5:179228859-179228909	HEK293	kidney:	embryo
45	chr5:179228859-179228909	AG04450	lung:	fetal
46	chr5:179228859-179228909	MCF10A-Er-Src	breast:	n/a
47	chr5:179228859-179228909	SK-N-MC	brain:	n/a
48	chr5:179228859-179228909	ProgFib	skin:	n/a
49	chr5:179228859-179228909	CMK	blood:	n/a
50	chr5:179228859-179228909	PrEC	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179227703..179229883-chr5:179285735..179289127,3	K562	blood:
2	chr5:179125163..179127622-chr5:179228110..179231035,2	K562	blood:
3	chr5:179227831..179231343-chr5:179333679..179336075,3	MCF-7	breast:
4	chr5:179227703..179229883-chr5:179285735..179288229,2	K562	blood:
5	chr5:179159678..179161359-chr5:179228559..179231556,2	MCF-7	breast:
6	chr5:179049178..179050682-chr5:179227339..179229062,2	MCF-7	breast:
7	chr5:179197599..179200377-chr5:179228822..179231191,2	MCF-7	breast:

No data

Variant related genes	Relation type
MGAT4B	TF binding region
MIR1229	TF binding region
SQSTM1	TF binding region
MIR1229	CpG island
MGAT4B	CpG island
SQSTM1	CpG island
ENSG00000127022	Chromatin interaction
ENSG00000169045	Chromatin interaction
ENSG00000161021	Chromatin interaction
ENSG00000245317	Chromatin interaction
ENSG00000197226	Chromatin interaction
ENSG00000161010	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs58773990	0.89[AMR][1000 genomes]
rs73351608	0.89[AMR][1000 genomes]
rs73351620	0.89[AMR][1000 genomes]

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	nsv949554	chr5:178832325-179309513	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
2	nsv883270	chr5:178951106-179350387	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
3	nsv531997	chr5:179107599-179588082	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	339 gene(s)	inside rSNPs	diseases
4	nsv469579	chr5:179184831-179360191	Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
5	nsv883274	chr5:179186397-179310330	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
6	nsv883275	chr5:179193598-179267783	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
7	nsv883276	chr5:179193598-179310330	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS 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 miRNA target site	178 gene(s)	inside rSNPs	diseases
8	nsv883277	chr5:179193598-179350387	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
9	nsv823361	chr5:179213324-179251243	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
10	nsv600660	chr5:179214251-179231248	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription 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	149 gene(s)	inside rSNPs	diseases
11	nsv883278	chr5:179214818-179238794	Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	154 gene(s)	inside rSNPs	diseases
12	nsv883279	chr5:179214818-179248774	Enhancers Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
13	nsv870188	chr5:179218824-179235424	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	154 gene(s)	inside rSNPs	diseases
14	nsv600662	chr5:179220010-179231248	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
15	nsv883280	chr5:179220010-179238794	Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking 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	154 gene(s)	inside rSNPs	diseases
16	nsv883281	chr5:179220010-179250500	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
17	nsv883282	chr5:179220638-179231248	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
18	nsv883283	chr5:179220638-179231681	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
19	nsv883284	chr5:179220638-179246415	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription 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 miRNA	158 gene(s)	inside rSNPs	diseases
20	nsv600665	chr5:179221789-179231248	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
21	nsv600666	chr5:179221789-179231681	Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
22	nsv600667	chr5:179223023-179229039	Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	148 gene(s)	inside rSNPs	diseases
23	nsv883285	chr5:179223023-179238794	Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	153 gene(s)	inside rSNPs	diseases
24	nsv600668	chr5:179227865-179242581	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr5:179223800-179229600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:179223800-179231600	Weak transcription	Fetal Kidney	kidney
3	chr5:179223800-179231600	Weak transcription	Psoas Muscle	Psoas
4	chr5:179224000-179229000	Strong transcription	A549	lung
5	chr5:179224000-179229000	Strong transcription	NHLF	lung
6	chr5:179224000-179229200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:179224000-179229200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr5:179224000-179229200	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr5:179224000-179229400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:179224000-179229600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:179224000-179230000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:179224000-179230000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:179224000-179230000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr5:179224000-179230800	Weak transcription	Right Atrium	heart
15	chr5:179224000-179232200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr5:179224200-179229000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:179224200-179229000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr5:179224200-179229000	Weak transcription	GM12878-XiMat	blood
19	chr5:179224200-179229600	Weak transcription	NH-A	brain
20	chr5:179224200-179230000	Strong transcription	Brain Germinal Matrix	brain
21	chr5:179224400-179229000	Strong transcription	Gastric	stomach
22	chr5:179224400-179229000	Weak transcription	Hela-S3	cervix
23	chr5:179224400-179229200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:179224400-179229200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:179224400-179229200	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr5:179224400-179229600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:179225400-179229200	Strong transcription	Fetal Intestine Large	intestine
28	chr5:179226200-179232200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:179226800-179233200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr5:179227000-179229400	Weak transcription	Primary B cells from cord blood	blood
31	chr5:179227000-179230800	Weak transcription	Fetal Brain Male	brain
32	chr5:179227200-179229000	Weak transcription	Stomach Mucosa	stomach
33	chr5:179227200-179230200	Weak transcription	HUVEC	blood vessel
34	chr5:179227200-179231000	Weak transcription	HSMMtube	muscle
35	chr5:179227200-179231800	Weak transcription	Brain Substantia Nigra	brain
36	chr5:179227400-179229000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr5:179227400-179229000	Weak transcription	NHDF-Ad	bronchial
38	chr5:179227400-179230200	Weak transcription	Thymus	Thymus
39	chr5:179227600-179229200	Weak transcription	Brain Angular Gyrus	brain
40	chr5:179227600-179230000	Weak transcription	Primary T cells from cord blood	blood
41	chr5:179227600-179230000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr5:179227600-179230000	Weak transcription	HSMM	muscle
43	chr5:179227600-179230200	Weak transcription	Fetal Lung	lung
44	chr5:179227600-179232000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr5:179227800-179229400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:179227800-179232000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:179227800-179232200	Enhancers	Fetal Heart	heart
48	chr5:179228000-179229600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr5:179228000-179229800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:179228000-179230800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood

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