Variant report

Variant	nsv517302
Chromosome Location	chr5:177383782-177400248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:150)
CpG islands
(count:672)
Chromatin interactive
region (count:2)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:150 , 50 per page) page: 1 2 3

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	ATF1	chr5:177384217-177384416	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	CHD2	chr5:177385654-177386621	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr5:177385796-177386503	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr5:177400180-177400330	HVMF	connective:	n/a	n/a
10	CTCF	chr5:177388232-177388305	GM12891	blood:	n/a	n/a
11	CTCF	chr5:177388177-177388209	GM13976	blood:	n/a	n/a
12	CTCF	chr5:177387480-177387630	HEEpiC	esophagus:	n/a	n/a
13	E2F6	chr5:177395613-177396232	H1-hESC	embryonic stem cell:	n/a	n/a
14	EBF1	chr5:177388374-177388646	GM12878	blood:	n/a	n/a
15	EBF1	chr5:177388394-177388697	GM12878	blood:	n/a	n/a
16	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
17	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
18	ELK1	chr5:177396027-177396050	GM12878	blood:	n/a	n/a
19	EP300	chr5:177388723-177388889	GM12878	blood:	n/a	n/a
20	EP300	chr5:177388317-177389303	GM12878	blood:	n/a	n/a
21	EP300	chr5:177388433-177388700	GM12878	blood:	n/a	n/a
22	EP300	chr5:177385764-177386240	H1-hESC	embryonic stem cell:	n/a	n/a
23	FAM48A	chr5:177396793-177397111	GM12878	blood:	n/a	n/a
24	FOS	chr5:177397637-177398024	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr5:177397636-177398049	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr5:177394372-177394618	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
27	FOS	chr5:177394282-177394621	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
28	FOS	chr5:177400238-177400562	MCF10A-Er-Src	breast:	n/a	chr5:177400265-177400276
29	FOS	chr5:177397715-177398028	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:177397617-177398046	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:177394165-177394785	HUVEC	blood vessel:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
32	FOS	chr5:177394271-177394598	MCF10A-Er-Src	breast:	n/a	chr5:177394428-177394439 chr5:177394458-177394469
33	FOSL2	chr5:177388691-177389165	HepG2	liver:	n/a	n/a
34	FOSL2	chr5:177389312-177389669	HepG2	liver:	n/a	n/a
35	FOSL2	chr5:177388331-177389250	HepG2	liver:	n/a	n/a
36	FOXA2	chr5:177388382-177389064	A549	lung:	n/a	n/a
37	FOXP2	chr5:177388320-177388702	PFSK-1	brain:	n/a	n/a
38	GABPA	chr5:177389386-177389519	Hela-S3	cervix:	n/a	n/a
39	GABPA	chr5:177388381-177388699	Hela-S3	cervix:	n/a	n/a
40	GABPA	chr5:177388409-177389100	Hela-S3	cervix:	n/a	n/a
41	GTF2F1	chr5:177397487-177397595	H1-hESC	embryonic stem cell:	n/a	n/a
42	GTF2F1	chr5:177398471-177398542	H1-hESC	embryonic stem cell:	n/a	n/a
43	GTF2F1	chr5:177393896-177394069	H1-hESC	embryonic stem cell:	n/a	n/a
44	GTF2F1	chr5:177385951-177386465	H1-hESC	embryonic stem cell:	n/a	n/a
45	HDAC2	chr5:177385812-177386245	H1-hESC	embryonic stem cell:	n/a	n/a
46	HEY1	chr5:177388337-177389219	K562	blood:	n/a	n/a
47	HEY1	chr5:177388427-177388755	K562	blood:	n/a	n/a
48	HMGN3	chr5:177393339-177393373	K562	blood:	n/a	n/a
49	IRF4	chr5:177388325-177389308	GM12878	blood:	n/a	n/a
50	IRF4	chr5:177388273-177389569	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177387796-177387846	AG09319	gingival:	n/a
2	chr5:177387796-177387846	AG09319	gingival:	n/a
3	chr5:177396838-177396888	HRPEpiC	eye:	n/a
4	chr5:177396838-177396888	HCM	heart:	n/a
5	chr5:177391178-177391228	PFSK-1	brain:	n/a
6	chr5:177398433-177398483	HEK293	kidney:	embryo
7	chr5:177395755-177395805	AoSMC	blood vessel:	n/a
8	chr5:177391705-177391755	NH-A	brain:	n/a
9	chr5:177398433-177398483	SAEC	small airway:	n/a
10	chr5:177398429-177398479	HAEpiC	amniotic membrane:	n/a
11	chr5:177399722-177399772	SK-N-SH_RA	brain:	n/a
12	chr5:177399722-177399772	HUVEC	blood vessel:	n/a
13	chr5:177398433-177398483	T-47D	breast:	n/a
14	chr5:177398433-177398483	GM12892	blood:	n/a
15	chr5:177387597-177387647	AoSMC	blood vessel:	n/a
16	chr5:177391705-177391755	RPTEC	kidney:	n/a
17	chr5:177387682-177387732	HEK293	kidney:	embryo
18	chr5:177387796-177387846	ProgFib	skin:	n/a
19	chr5:177385478-177385528	HUVEC	blood vessel:	n/a
20	chr5:177387597-177387647	AG04450	lung:	fetal
21	chr5:177391178-177391228	H1-hESC	embryonic stem cell:	embryo
22	chr5:177385478-177385528	PANC-1	pancreas:	n/a
23	chr5:177387597-177387647	AG04449	skin:	fetal
24	chr5:177391178-177391228	RPTEC	kidney:	n/a
25	chr5:177398429-177398479	NHDF-neo	bronchial:	n/a
26	chr5:177395755-177395805	SK-N-MC	brain:	n/a
27	chr5:177385478-177385528	ECC-1	luminal epithelium:	n/a
28	chr5:177387682-177387732	HepG2	liver:	n/a
29	chr5:177395755-177395805	MCF-7	breast:	n/a
30	chr5:177398433-177398483	GM06990	blood:	n/a
31	chr5:177387597-177387647	HEEpiC	esophagus:	n/a
32	chr5:177396838-177396888	PrEC	prostate:	n/a
33	chr5:177391705-177391755	HRPEpiC	eye:	n/a
34	chr5:177395755-177395805	AG09309	skin:	n/a
35	chr5:177396838-177396888	H1-hESC	embryonic stem cell:	embryo
36	chr5:177387796-177387846	ovcar-3	ovarian:	n/a
37	chr5:177398429-177398479	NB4	blood:	n/a
38	chr5:177387682-177387732	PrEC	prostate:	n/a
39	chr5:177385478-177385528	IMR90	lung:	fetal
40	chr5:177391178-177391228	NB4	blood:	n/a
41	chr5:177391705-177391755	HepG2	liver:	n/a
42	chr5:177391178-177391228	HCPEpiC	choroid plexus:	n/a
43	chr5:177387597-177387647	HCPEpiC	choroid plexus:	n/a
44	chr5:177385478-177385528	SKMC	muscle:	n/a
45	chr5:177395755-177395805	AG10803	skin:	n/a
46	chr5:177387796-177387846	GM12878	blood:	n/a
47	chr5:177399722-177399772	K562	blood:	n/a
48	chr5:177387597-177387647	K562	blood:	n/a
49	chr5:177385478-177385528	GM06990	blood:	n/a
50	chr5:177387597-177387647	ProgFib	skin:	n/a

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

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:

(count:11 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1006 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11249784	chr5:177383782-177383783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs560806854	chr5:177383795-177383796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370991870	chr5:177383812-177383813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192331165	chr5:177383815-177383816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545843961	chr5:177383827-177383828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564058046	chr5:177383875-177383876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531304897	chr5:177383886-177383887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549635206	chr5:177383895-177383896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183235665	chr5:177383925-177383926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529114873	chr5:177383953-177383954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188841704	chr5:177383958-177383959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527279207	chr5:177383996-177383997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192671765	chr5:177383997-177383998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56306562	chr5:177384016-177384017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539329953	chr5:177384024-177384025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183398490	chr5:177384049-177384050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13166816	chr5:177384084-177384085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538192377	chr5:177384094-177384095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71760340	chr5:177384138-177384139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148625501	chr5:177384141-177384142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369208744	chr5:177384142-177384143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150658170	chr5:177384143-177384144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556391091	chr5:177384151-177384152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539697951	chr5:177384177-177384178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59722055	chr5:177384212-177384213	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556723804	chr5:177384254-177384255	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533916721	chr5:177384294-177384295	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114988911	chr5:177384302-177384303	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554387247	chr5:177384309-177384310	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572811675	chr5:177384346-177384347	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186685995	chr5:177384364-177384365	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564744203	chr5:177384404-177384405	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531214560	chr5:177384405-177384406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386695406	chr5:177384417-177384418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28401381	chr5:177384418-177384419	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73807314	chr5:177384430-177384431	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191306215	chr5:177384431-177384432	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559136122	chr5:177384440-177384441	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532933011	chr5:177384464-177384465	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142311947	chr5:177384469-177384470	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7445906	chr5:177384514-177384515	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs4077204	chr5:177384542-177384543	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144409748	chr5:177384568-177384569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145926665	chr5:177384643-177384644	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs568489678	chr5:177384645-177384646	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs4077205	chr5:177384649-177384650	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs35713651	chr5:177384668-177384669	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs5873589	chr5:177384670-177384671	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs183862051	chr5:177384678-177384679	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs574510139	chr5:177384684-177384685	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:138 , 50 per page) page: 1 2 3

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	chr5:177371600-177383800	Weak transcription	Liver	Liver
4	chr5:177371600-177385200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr5:177371600-177389600	Weak transcription	Brain Germinal Matrix	brain
6	chr5:177371800-177384200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:177371800-177387400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr5:177371800-177387600	Weak transcription	Pancreas	Pancrea
9	chr5:177371800-177387800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:177371800-177388200	Weak transcription	Gastric	stomach
11	chr5:177371800-177390200	Weak transcription	Primary T cells from cord blood	blood
12	chr5:177371800-177390800	Weak transcription	Ovary	ovary
13	chr5:177371800-177392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr5:177371800-177394200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:177371800-177394200	Weak transcription	Right Ventricle	heart
16	chr5:177372000-177385200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:177372000-177385400	Weak transcription	NHDF-Ad	bronchial
18	chr5:177372200-177390000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:177372400-177385600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr5:177372600-177385600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:177372600-177388200	Weak transcription	Esophagus	oesophagus
22	chr5:177374200-177384400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:177374400-177385200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:177375200-177387600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:177375400-177385200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:177375400-177385200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr5:177378000-177388400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr5:177378600-177385200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr5:177378600-177387600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:177379200-177385800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:177379200-177386000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:177379200-177387600	Weak transcription	NHLF	lung
33	chr5:177379200-177392400	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr5:177382600-177383800	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr5:177382800-177384600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:177383200-177384800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr5:177383600-177384600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr5:177383800-177393600	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr5:177384200-177384400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr5:177384200-177384800	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:177384400-177385600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr5:177384400-177386800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:177384600-177384800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:177384600-177385000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr5:177384800-177385200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:177384800-177385400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:177385000-177389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr5:177385200-177386200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:177385200-177386400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:177385200-177386400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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