Variant report

Variant	esv2763926
Chromosome Location	chr5:177390075-177401509
allele	n/a
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	ATF1	chr5:177397729-177397797	K562	blood:	n/a	n/a
2	CTCF	chr5:177400180-177400330	HVMF	connective:	n/a	n/a
3	E2F6	chr5:177395613-177396232	H1-hESC	embryonic stem cell:	n/a	n/a
4	EGR1	chr5:177392990-177393314	K562	blood:	n/a	chr5:177393182-177393192 chr5:177393180-177393194 chr5:177393182-177393192 chr5:177393186-177393193 chr5:177393179-177393194 chr5:177393180-177393193 chr5:177393183-177393192 chr5:177393181-177393192 chr5:177393180-177393193 chr5:177393180-177393193
5	EGR1	chr5:177393017-177393316	K562	blood:	n/a	chr5:177393182-177393192 chr5:177393180-177393194 chr5:177393182-177393192 chr5:177393186-177393193 chr5:177393179-177393194 chr5:177393180-177393193 chr5:177393183-177393192 chr5:177393181-177393192 chr5:177393180-177393193 chr5:177393180-177393193
6	ELK1	chr5:177396027-177396050	GM12878	blood:	n/a	n/a
7	FAM48A	chr5:177396793-177397111	GM12878	blood:	n/a	n/a
8	FOS	chr5:177397636-177398049	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr5:177394271-177394598	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
10	FOS	chr5:177394372-177394618	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
11	FOS	chr5:177397637-177398024	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr5:177400238-177400562	MCF10A-Er-Src	breast:	n/a	chr5:177400265-177400276
13	FOS	chr5:177397715-177398028	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr5:177400301-177400512	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr5:177394282-177394621	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
16	FOS	chr5:177394165-177394785	HUVEC	blood vessel:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
17	FOS	chr5:177400252-177400562	MCF10A-Er-Src	breast:	n/a	chr5:177400265-177400276
18	FOS	chr5:177397617-177398046	MCF10A-Er-Src	breast:	n/a	n/a
19	GTF2F1	chr5:177398471-177398542	H1-hESC	embryonic stem cell:	n/a	n/a
20	GTF2F1	chr5:177393896-177394069	H1-hESC	embryonic stem cell:	n/a	n/a
21	GTF2F1	chr5:177397487-177397595	H1-hESC	embryonic stem cell:	n/a	n/a
22	HMGN3	chr5:177393339-177393373	K562	blood:	n/a	n/a
23	JUND	chr5:177397840-177397932	K562	blood:	n/a	chr5:177397866-177397877
24	JUND	chr5:177397756-177398021	HepG2	liver:	n/a	chr5:177397866-177397877
25	MAFF	chr5:177398645-177398823	HepG2	liver:	n/a	chr5:177398782-177398800 chr5:177398741-177398759
26	MAFF	chr5:177397620-177397786	K562	blood:	n/a	n/a
27	MAFF	chr5:177397589-177397813	HepG2	liver:	n/a	n/a
28	MAFK	chr5:177397560-177397850	HepG2	liver:	n/a	n/a
29	MAFK	chr5:177398613-177398771	IMR90	lung:	n/a	n/a
30	MAFK	chr5:177398620-177398811	HepG2	liver:	n/a	n/a
31	MAFK	chr5:177398653-177398681	HepG2	liver:	n/a	n/a
32	MAFK	chr5:177397525-177397847	HepG2	liver:	n/a	n/a
33	MAX	chr5:177395662-177395890	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAX	chr5:177395830-177395965	NB4	blood:	n/a	n/a
35	MAZ	chr5:177395722-177395843	HepG2	liver:	n/a	n/a
36	NFIC	chr5:177394340-177394980	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr5:177398189-177398247	A549	lung:	n/a	n/a
38	POLR2A	chr5:177395942-177395955	MCF-7	breast:	n/a	n/a
39	POLR2A	chr5:177395978-177396009	MCF-7	breast:	n/a	n/a
40	POLR2A	chr5:177398201-177398338	A549	lung:	n/a	n/a
41	POLR2A	chr5:177395963-177395975	MCF-7	breast:	n/a	n/a
42	POLR2A	chr5:177399102-177399164	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr5:177398969-177399042	Gliobla	brain:	n/a	n/a
44	POLR2A	chr5:177396012-177396019	MCF-7	breast:	n/a	n/a
45	POLR2A	chr5:177398229-177398312	A549	lung:	n/a	n/a
46	POLR2A	chr5:177398231-177398319	A549	lung:	n/a	n/a
47	POLR2A	chr5:177398268-177398306	K562	blood:	n/a	n/a
48	RFX5	chr5:177391731-177391769	K562	blood:	n/a	n/a
49	STAT3	chr5:177394393-177394599	MCF10A-Er-Src	breast:	n/a	n/a
50	TCF12	chr5:177394291-177394890	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177396838-177396888	GM12878	blood:	n/a
2	chr5:177396838-177396888	GM12878	blood:	n/a
3	chr5:177398429-177398479	K562	blood:	n/a
4	chr5:177396838-177396888	HEK293	kidney:	embryo
5	chr5:177396838-177396888	PFSK-1	brain:	n/a
6	chr5:177391705-177391755	HRPEpiC	eye:	n/a
7	chr5:177398433-177398483	HAEpiC	amniotic membrane:	n/a
8	chr5:177391178-177391228	SKMC	muscle:	n/a
9	chr5:177395755-177395805	CMK	blood:	n/a
10	chr5:177398433-177398483	RPTEC	kidney:	n/a
11	chr5:177391178-177391228	ovcar-3	ovarian:	n/a
12	chr5:177396838-177396888	HMEC	breast:	n/a
13	chr5:177396838-177396888	A549	lung:	n/a
14	chr5:177391705-177391755	AG04450	lung:	fetal
15	chr5:177396838-177396888	MCF10A-Er-Src	breast:	n/a
16	chr5:177391178-177391228	Hepatocyte	liver:	n/a
17	chr5:177391705-177391755	HCF	heart:	n/a
18	chr5:177398433-177398483	IMR90	lung:	fetal
19	chr5:177396838-177396888	HIPEpiC	eye:	n/a
20	chr5:177399722-177399772	RPTEC	kidney:	n/a
21	chr5:177399722-177399772	HUVEC	blood vessel:	n/a
22	chr5:177395755-177395805	HRE	kidney:	n/a
23	chr5:177399722-177399772	AG10803	skin:	n/a
24	chr5:177398429-177398479	ProgFib	skin:	n/a
25	chr5:177398429-177398479	HEEpiC	esophagus:	n/a
26	chr5:177391178-177391228	HCT-116	colon:	n/a
27	chr5:177398429-177398479	NHBE	bronchial:	n/a
28	chr5:177398429-177398479	HNPCEpiC	eye:	n/a
29	chr5:177395755-177395805	HCT-116	colon:	n/a
30	chr5:177399722-177399772	NB4	blood:	n/a
31	chr5:177391705-177391755	Hepatocyte	liver:	n/a
32	chr5:177399722-177399772	IMR90	lung:	fetal
33	chr5:177398429-177398479	GM19239	blood:	n/a
34	chr5:177395755-177395805	AG04450	lung:	fetal
35	chr5:177391178-177391228	AG04449	skin:	fetal
36	chr5:177391178-177391228	IMR90	lung:	fetal
37	chr5:177396838-177396888	HCM	heart:	n/a
38	chr5:177391178-177391228	K562	blood:	n/a
39	chr5:177396838-177396888	CMK	blood:	n/a
40	chr5:177398429-177398479	SK-N-SH	brain:	n/a
41	chr5:177391705-177391755	ECC-1	luminal epithelium:	n/a
42	chr5:177398429-177398479	A549	lung:	n/a
43	chr5:177399722-177399772	U87	brain:	n/a
44	chr5:177398429-177398479	HUVEC	blood vessel:	n/a
45	chr5:177396838-177396888	HCPEpiC	choroid plexus:	n/a
46	chr5:177395755-177395805	Jurkat	blood:	n/a
47	chr5:177398433-177398483	CMK	blood:	n/a
48	chr5:177391178-177391228	HUVEC	blood vessel:	n/a
49	chr5:177398429-177398479	HIPEpiC	eye:	n/a
50	chr5:177398433-177398483	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177399899..177402240-chr5:177658876..177660987,2	K562	blood:
2	chr5:177389362..177391423-chr5:177551819..177554278,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM153C-2	chr5:177389519-177390144	XLOC_004670
2	lnc-FAM153C-4	chr5:177390828-177390961	ENSG00000249684.1

Variant related genes	Relation type
SUDS3P1	TF binding region
SUDS3P1	CpG island
ENSG00000175309	chromatin interactions

Extended variants
information (count: 628 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6898048	chr5:177390075-177390076	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147155098	chr5:177390079-177390080	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
3	rs552622387	chr5:177390127-177390128	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
4	rs374836206	chr5:177390144-177390145	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
5	rs557641167	chr5:177390206-177390207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140402008	chr5:177390246-177390247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4580789	chr5:177390271-177390272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs117243247	chr5:177390300-177390301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543877540	chr5:177390337-177390338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201497841	chr5:177390340-177390341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562072880	chr5:177390352-177390353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555206880	chr5:177390380-177390381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529254105	chr5:177390409-177390410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536873993	chr5:177390414-177390415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547931765	chr5:177390415-177390416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559579841	chr5:177390444-177390445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557403283	chr5:177390479-177390480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181478704	chr5:177390481-177390482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6601190	chr5:177390482-177390483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369231687	chr5:177390495-177390496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186116198	chr5:177390507-177390508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537358465	chr5:177390508-177390509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549220201	chr5:177390511-177390512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190239188	chr5:177390527-177390528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6874403	chr5:177390533-177390534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373481333	chr5:177390555-177390556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537013823	chr5:177390597-177390598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577642618	chr5:177390599-177390600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553448706	chr5:177390607-177390608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112705628	chr5:177390625-177390626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147781642	chr5:177390629-177390630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575467808	chr5:177390633-177390634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182822762	chr5:177390647-177390648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573277326	chr5:177390661-177390662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542943829	chr5:177390671-177390672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561136062	chr5:177390672-177390673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545674892	chr5:177390673-177390674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541418104	chr5:177390674-177390675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6601191	chr5:177390678-177390679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187550808	chr5:177390690-177390691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531105213	chr5:177390720-177390721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78693149	chr5:177390724-177390725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377696329	chr5:177390749-177390750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73807316	chr5:177390777-177390778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563735060	chr5:177390803-177390804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530982601	chr5:177390813-177390814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148477325	chr5:177390853-177390854	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs373233410	chr5:177390865-177390866	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs567604793	chr5:177390874-177390875	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs114104337	chr5:177390880-177390881	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177368200-177396400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:177371000-177393000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr5:177371800-177390200	Weak transcription	Primary T cells from cord blood	blood
4	chr5:177371800-177390800	Weak transcription	Ovary	ovary
5	chr5:177371800-177392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr5:177371800-177394200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:177371800-177394200	Weak transcription	Right Ventricle	heart
8	chr5:177379200-177392400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr5:177383800-177393600	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:177386400-177393600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:177386400-177394400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:177386600-177395600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:177386800-177395800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr5:177388400-177391200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:177388400-177397400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr5:177388400-177411400	Weak transcription	Gastric	stomach
17	chr5:177388600-177393200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr5:177388800-177390800	Weak transcription	Esophagus	oesophagus
19	chr5:177390000-177390200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:177390200-177390800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:177390800-177391000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:177390800-177391600	Strong transcription	Esophagus	oesophagus
23	chr5:177391000-177391200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:177391000-177391600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr5:177391200-177391800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:177391200-177402400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:177391600-177392000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr5:177391600-177393200	Weak transcription	Esophagus	oesophagus
29	chr5:177391800-177395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:177393000-177393200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr5:177393000-177394200	Enhancers	Fetal Brain Male	brain
32	chr5:177393200-177393400	Enhancers	Esophagus	oesophagus
33	chr5:177393200-177393800	Enhancers	Pancreas	Pancrea
34	chr5:177393600-177395200	Enhancers	HUVEC	blood vessel
35	chr5:177393800-177394800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr5:177394000-177394800	Enhancers	NHEK	skin
37	chr5:177394200-177394600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:177394200-177394800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:177394600-177394800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:177395600-177396000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:177395600-177396000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:177395600-177396200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:177395800-177396000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr5:177396200-177397800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:177397400-177398600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr5:177397800-177398400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:177398000-177398200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:177398000-177398600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr5:177398200-177398600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
50	chr5:177398200-177398600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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