Variant report

Variant	esv2760946
Chromosome Location	chr5:177379490-177401509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:673)
Chromatin interactive
region (count:2)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:177384217-177384416	K562	blood:	n/a	n/a
2	ATF1	chr5:177397729-177397797	K562	blood:	n/a	n/a
3	BACH1	chr5:177385596-177386218	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:177388724-177389177	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:177388361-177389261	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:177388404-177388659	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:177382431-177382600	GM12878	blood:	n/a	n/a
8	BHLHE40	chr5:177382002-177382214	GM12878	blood:	n/a	n/a
9	CHD2	chr5:177385654-177386621	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr5:177385796-177386503	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr5:177387480-177387630	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr5:177388232-177388305	GM12891	blood:	n/a	n/a
13	CTCF	chr5:177382307-177382384	GM13976	blood:	n/a	n/a
14	CTCF	chr5:177400180-177400330	HVMF	connective:	n/a	n/a
15	CTCF	chr5:177388177-177388209	GM13976	blood:	n/a	n/a
16	E2F6	chr5:177395613-177396232	H1-hESC	embryonic stem cell:	n/a	n/a
17	EBF1	chr5:177381879-177382718	GM12878	blood:	n/a	chr5:177382509-177382520
18	EBF1	chr5:177382341-177382610	GM12878	blood:	n/a	chr5:177382509-177382520
19	EBF1	chr5:177388374-177388646	GM12878	blood:	n/a	n/a
20	EBF1	chr5:177382327-177382652	GM12878	blood:	n/a	chr5:177382509-177382520
21	EBF1	chr5:177388394-177388697	GM12878	blood:	n/a	n/a
22	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
23	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
24	ELK1	chr5:177396027-177396050	GM12878	blood:	n/a	n/a
25	EP300	chr5:177388723-177388889	GM12878	blood:	n/a	n/a
26	EP300	chr5:177385764-177386240	H1-hESC	embryonic stem cell:	n/a	n/a
27	EP300	chr5:177388317-177389303	GM12878	blood:	n/a	n/a
28	EP300	chr5:177388433-177388700	GM12878	blood:	n/a	n/a
29	FAM48A	chr5:177396793-177397111	GM12878	blood:	n/a	n/a
30	FOS	chr5:177400252-177400562	MCF10A-Er-Src	breast:	n/a	chr5:177400265-177400276
31	FOS	chr5:177397637-177398024	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:177400301-177400512	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:177394282-177394621	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
34	FOS	chr5:177397617-177398046	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:177394165-177394785	HUVEC	blood vessel:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
36	FOS	chr5:177400238-177400562	MCF10A-Er-Src	breast:	n/a	chr5:177400265-177400276
37	FOS	chr5:177394372-177394618	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
38	FOS	chr5:177397636-177398049	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:177394271-177394598	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
40	FOS	chr5:177397715-177398028	MCF10A-Er-Src	breast:	n/a	n/a
41	FOSL2	chr5:177389312-177389669	HepG2	liver:	n/a	n/a
42	FOSL2	chr5:177388331-177389250	HepG2	liver:	n/a	n/a
43	FOSL2	chr5:177388691-177389165	HepG2	liver:	n/a	n/a
44	FOXA2	chr5:177388382-177389064	A549	lung:	n/a	n/a
45	FOXP2	chr5:177388320-177388702	PFSK-1	brain:	n/a	n/a
46	GABPA	chr5:177388409-177389100	Hela-S3	cervix:	n/a	n/a
47	GABPA	chr5:177389386-177389519	Hela-S3	cervix:	n/a	n/a
48	GABPA	chr5:177388381-177388699	Hela-S3	cervix:	n/a	n/a
49	GTF2F1	chr5:177393896-177394069	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr5:177385951-177386465	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177387597-177387647	NHDF-neo	bronchial:	n/a
2	chr5:177387682-177387732	HAEpiC	amniotic membrane:	n/a
3	chr5:177387597-177387647	NHDF-neo	bronchial:	n/a
4	chr5:177387682-177387732	HAEpiC	amniotic membrane:	n/a
5	chr5:177395755-177395805	Hela-S3	cervix:	n/a
6	chr5:177391705-177391755	AoSMC	blood vessel:	n/a
7	chr5:177391705-177391755	ProgFib	skin:	n/a
8	chr5:177385478-177385528	HUVEC	blood vessel:	n/a
9	chr5:177395755-177395805	GM12878	blood:	n/a
10	chr5:177398429-177398479	GM12891	blood:	n/a
11	chr5:177387682-177387732	HRE	kidney:	n/a
12	chr5:177387597-177387647	AG09309	skin:	n/a
13	chr5:177399722-177399772	HIPEpiC	eye:	n/a
14	chr5:177399722-177399772	HAEpiC	amniotic membrane:	n/a
15	chr5:177391705-177391755	MCF10A-Er-Src	breast:	n/a
16	chr5:177396838-177396888	AG09309	skin:	n/a
17	chr5:177398429-177398479	HNPCEpiC	eye:	n/a
18	chr5:177395755-177395805	BE2_C	brain:	n/a
19	chr5:177396838-177396888	NB4	blood:	n/a
20	chr5:177391178-177391228	PANC-1	pancreas:	n/a
21	chr5:177391705-177391755	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:177396838-177396888	AG09319	gingival:	n/a
23	chr5:177398433-177398483	AG10803	skin:	n/a
24	chr5:177396838-177396888	T-47D	breast:	n/a
25	chr5:177387682-177387732	HRPEpiC	eye:	n/a
26	chr5:177399722-177399772	HNPCEpiC	eye:	n/a
27	chr5:177396838-177396888	HRPEpiC	eye:	n/a
28	chr5:177398429-177398479	NT2-D1	testis:	n/a
29	chr5:177391178-177391228	NB4	blood:	n/a
30	chr5:177396838-177396888	HCF	heart:	n/a
31	chr5:177391705-177391755	HMEC	breast:	n/a
32	chr5:177387796-177387846	Caco-2	colon:	n/a
33	chr5:177387682-177387732	NH-A	brain:	n/a
34	chr5:177396838-177396888	HRE	kidney:	n/a
35	chr5:177398429-177398479	RPTEC	kidney:	n/a
36	chr5:177398433-177398483	HCT-116	colon:	n/a
37	chr5:177391178-177391228	T-47D	breast:	n/a
38	chr5:177387682-177387732	HRCEpiC	kidney:	n/a
39	chr5:177399722-177399772	AG09309	skin:	n/a
40	chr5:177395755-177395805	NHBE	bronchial:	n/a
41	chr5:177395755-177395805	GM12892	blood:	n/a
42	chr5:177391705-177391755	Jurkat	blood:	n/a
43	chr5:177387682-177387732	A549	lung:	n/a
44	chr5:177387682-177387732	BE2_C	brain:	n/a
45	chr5:177398433-177398483	GM19239	blood:	n/a
46	chr5:177387597-177387647	Caco-2	colon:	n/a
47	chr5:177387682-177387732	HNPCEpiC	eye:	n/a
48	chr5:177387597-177387647	HL-60	blood:	n/a
49	chr5:177398433-177398483	CMK	blood:	n/a
50	chr5:177387682-177387732	PrEC	prostate:	n/a

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

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

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM153C-4	chr5:177390828-177390961	ENSG00000249684.1
2	lnc-FAM153C-2	chr5:177389519-177390144	XLOC_004670
3	lnc-FAM153C-4	chr5:177386720-177387150	ENSG00000249684.1
4	lnc-FAM153C-4	chr5:177384610-177384680	ENSG00000249684.1
5	lnc-FAM153C-4	chr5:177384610-177384751	ENSG00000249684.1
6	lnc-PROP1-2	chr5:177388524-177388667	XLOC_005099
7	lnc-FAM153C-4	chr5:177384610-177384760	ENSG00000249684.1
8	lnc-FAM153C-5	chr5:177384610-177384979	NONHSAT105484
9	lnc-PROP1-2	chr5:177388755-177388871	XLOC_005099
10	lnc-FAM153C-2	chr5:177389362-177389432	XLOC_004670
11	lnc-FAM153C-4	chr5:177384610-177384680	ENSG00000249684.1
12	lnc-FAM153C-4	chr5:177380166-177380293	ENSG00000249684.1

No data

Variant related genes	Relation type
ENSG00000249684	TF binding region
SUDS3P1	TF binding region
ENSG00000249684	CpG island
SUDS3P1	CpG island
ENSG00000175309	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72648823	chr5:177379495-177379496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142372272	chr5:177379496-177379497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376098265	chr5:177379504-177379505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74993175	chr5:177379521-177379522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201677559	chr5:177379533-177379534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189276467	chr5:177379536-177379537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575891386	chr5:177379574-177379575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111960884	chr5:177379588-177379589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75703505	chr5:177379618-177379619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13178827	chr5:177379645-177379646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs113489187	chr5:177379649-177379650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13168110	chr5:177379653-177379654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182075645	chr5:177379656-177379657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111844012	chr5:177379691-177379692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13156056	chr5:177379746-177379747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13156062	chr5:177379757-177379758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28680744	chr5:177379760-177379761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13156075	chr5:177379780-177379781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113518333	chr5:177379783-177379784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78397414	chr5:177379786-177379787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76949389	chr5:177379789-177379790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190762484	chr5:177379799-177379800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13172040	chr5:177379802-177379803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547194514	chr5:177379893-177379894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143759723	chr5:177379936-177379937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73807310	chr5:177379946-177379947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572320038	chr5:177379976-177379977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61661905	chr5:177379996-177379997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186251539	chr5:177380010-177380011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151099605	chr5:177380029-177380030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4540200	chr5:177380048-177380049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs191492420	chr5:177380049-177380050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145316717	chr5:177380056-177380057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371816918	chr5:177380080-177380081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535812801	chr5:177380081-177380082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553980622	chr5:177380082-177380083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572465494	chr5:177380083-177380084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546462332	chr5:177380120-177380121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558382433	chr5:177380129-177380130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182400912	chr5:177380130-177380131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544141404	chr5:177380133-177380134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562376726	chr5:177380136-177380137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11740554	chr5:177380181-177380182	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs142307331	chr5:177380191-177380192	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs369931712	chr5:177380196-177380197	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs559222251	chr5:177380206-177380207	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs532859186	chr5:177380228-177380229	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs559103674	chr5:177380231-177380232	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs551189040	chr5:177380234-177380235	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs187885051	chr5:177380251-177380252	Weak 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:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177368200-177396400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:177371000-177381800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:177371000-177393000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:177371600-177383800	Weak transcription	Liver	Liver
5	chr5:177371600-177385200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:177371600-177389600	Weak transcription	Brain Germinal Matrix	brain
7	chr5:177371800-177380600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr5:177371800-177384200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:177371800-177387400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:177371800-177387600	Weak transcription	Pancreas	Pancrea
11	chr5:177371800-177387800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:177371800-177388200	Weak transcription	Gastric	stomach
13	chr5:177371800-177390200	Weak transcription	Primary T cells from cord blood	blood
14	chr5:177371800-177390800	Weak transcription	Ovary	ovary
15	chr5:177371800-177392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr5:177371800-177394200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:177371800-177394200	Weak transcription	Right Ventricle	heart
18	chr5:177372000-177381800	Weak transcription	Lung	lung
19	chr5:177372000-177382800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr5:177372000-177385200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:177372000-177385400	Weak transcription	NHDF-Ad	bronchial
22	chr5:177372200-177390000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:177372400-177385600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:177372600-177385600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:177372600-177388200	Weak transcription	Esophagus	oesophagus
26	chr5:177374200-177384400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr5:177374400-177385200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr5:177375200-177387600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:177375400-177385200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr5:177375400-177385200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:177375600-177381000	Weak transcription	Thymus	Thymus
32	chr5:177378000-177388400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr5:177378600-177385200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr5:177378600-177387600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr5:177379000-177383000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr5:177379000-177383200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr5:177379200-177382600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr5:177379200-177383000	Weak transcription	Fetal Stomach	stomach
39	chr5:177379200-177385800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:177379200-177386000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr5:177379200-177387600	Weak transcription	NHLF	lung
42	chr5:177379200-177392400	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr5:177379400-177379600	Weak transcription	Spleen	Spleen
44	chr5:177381800-177382800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:177382600-177383800	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr5:177382800-177383200	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr5:177382800-177384600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:177383200-177383600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr5:177383200-177384800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr5:177383600-177384600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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