Variant report

Variant	nsv823352
Chromosome Location	chr5:178279625-178296623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:1101)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178286713-178287002	HepG2	liver:	n/a	n/a
2	ATF1	chr5:178286762-178287220	K562	blood:	n/a	n/a
3	ATF2	chr5:178286589-178286974	GM12878	blood:	n/a	n/a
4	ATF3	chr5:178286654-178287084	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr5:178286755-178287144	K562	blood:	n/a	n/a
6	BACH1	chr5:178286831-178287481	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr5:178286705-178287046	K562	blood:	n/a	n/a
8	BCLAF1	chr5:178286646-178287185	GM12878	blood:	n/a	n/a
9	BCLAF1	chr5:178286652-178287189	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:178286715-178287439	HepG2	liver:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
11	BHLHE40	chr5:178281482-178281689	HepG2	liver:	n/a	n/a
12	BHLHE40	chr5:178281355-178281697	K562	blood:	n/a	n/a
13	BHLHE40	chr5:178286636-178287416	K562	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
14	BHLHE40	chr5:178286530-178287352	GM12878	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
15	BRCA1	chr5:178286778-178287148	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:178286775-178286962	HepG2	liver:	n/a	n/a
17	CBX3	chr5:178286504-178287357	HCT-116	colon:	n/a	n/a
18	CBX3	chr5:178286622-178287208	K562	blood:	n/a	n/a
19	CCNT2	chr5:178281392-178281608	K562	blood:	n/a	n/a
20	CCNT2	chr5:178286759-178287496	K562	blood:	n/a	n/a
21	CEBPB	chr5:178286811-178287376	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:178293795-178293858	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:178285796-178285889	K562	blood:	n/a	n/a
24	CEBPD	chr5:178281357-178281709	K562	blood:	n/a	n/a
25	CEBPD	chr5:178286868-178287258	HepG2	liver:	n/a	n/a
26	CHD1	chr5:178286816-178287274	GM12878	blood:	n/a	n/a
27	CHD2	chr5:178286711-178287474	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr5:178286713-178287176	HepG2	liver:	n/a	n/a
29	CHD2	chr5:178281396-178281607	K562	blood:	n/a	n/a
30	CHD2	chr5:178286747-178287356	GM12878	blood:	n/a	n/a
31	CHD2	chr5:178286719-178287176	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr5:178286820-178287177	K562	blood:	n/a	n/a
33	CREB1	chr5:178286648-178287231	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr5:178286681-178287337	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr5:178286704-178287340	GM12878	blood:	n/a	n/a
36	CREB1	chr5:178286710-178287214	A549	lung:	n/a	n/a
37	CREB1	chr5:178286629-178287486	HepG2	liver:	n/a	n/a
38	CTCF	chr5:178286880-178287030	HVMF	connective:	n/a	n/a
39	CTCF	chr5:178287000-178287150	HAc	cerebellar:	n/a	n/a
40	CTCF	chr5:178286907-178286908	Gliobla	brain:	n/a	n/a
41	CTCF	chr5:178286831-178286988	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr5:178286869-178286966	GM12878	blood:	n/a	n/a
43	CTCF	chr5:178286780-178286930	GM12872	blood:	n/a	n/a
44	CTCF	chr5:178295575-178295582	GM13976	blood:	n/a	n/a
45	CTCF	chr5:178286861-178286906	Gliobla	brain:	n/a	n/a
46	CTCF	chr5:178286820-178286970	HRE	kidney:	n/a	n/a
47	CTCF	chr5:178286860-178287010	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr5:178286780-178286930	HFF	foreskin:	n/a	n/a
49	CTCF	chr5:178286800-178286950	BE2_C	brain:	n/a	n/a
50	CTCF	chr5:178286880-178287030	HMEC	breast:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178287767-178287817	GM06990	blood:	n/a
2	chr5:178288687-178288737	HRPEpiC	eye:	n/a
3	chr5:178286920-178286970	H1-hESC	embryonic stem cell:	embryo
4	chr5:178287767-178287817	GM06990	blood:	n/a
5	chr5:178288687-178288737	HRPEpiC	eye:	n/a
6	chr5:178286920-178286970	H1-hESC	embryonic stem cell:	embryo
7	chr5:178286892-178286942	HEEpiC	esophagus:	n/a
8	chr5:178283861-178283911	HCPEpiC	choroid plexus:	n/a
9	chr5:178286875-178286925	K562	blood:	n/a
10	chr5:178286857-178286907	SKMC	muscle:	n/a
11	chr5:178288625-178288675	SK-N-SH_RA	brain:	n/a
12	chr5:178283861-178283911	HL-60	blood:	n/a
13	chr5:178286875-178286925	GM12878	blood:	n/a
14	chr5:178287544-178287594	SK-N-MC	brain:	n/a
15	chr5:178286626-178286676	HMEC	breast:	n/a
16	chr5:178286626-178286676	IMR90	lung:	fetal
17	chr5:178285999-178286049	NHDF-neo	bronchial:	n/a
18	chr5:178287112-178287162	ovcar-3	ovarian:	n/a
19	chr5:178285999-178286049	HUVEC	blood vessel:	n/a
20	chr5:178286892-178286942	GM12878	blood:	n/a
21	chr5:178286920-178286970	ECC-1	luminal epithelium:	n/a
22	chr5:178286875-178286925	IMR90	lung:	fetal
23	chr5:178287112-178287162	HUVEC	blood vessel:	n/a
24	chr5:178288650-178288700	AoSMC	blood vessel:	n/a
25	chr5:178287544-178287594	NT2-D1	testis:	n/a
26	chr5:178287767-178287817	HUVEC	blood vessel:	n/a
27	chr5:178286892-178286942	Hepatocyte	liver:	n/a
28	chr5:178287767-178287817	HepG2	liver:	n/a
29	chr5:178283861-178283911	AG09309	skin:	n/a
30	chr5:178286920-178286970	NH-A	brain:	n/a
31	chr5:178286920-178286970	HRPEpiC	eye:	n/a
32	chr5:178288650-178288700	HL-60	blood:	n/a
33	chr5:178287544-178287594	HEEpiC	esophagus:	n/a
34	chr5:178285999-178286049	HMEC	breast:	n/a
35	chr5:178286892-178286942	ovcar-3	ovarian:	n/a
36	chr5:178286857-178286907	GM12891	blood:	n/a
37	chr5:178288687-178288737	PrEC	prostate:	n/a
38	chr5:178286892-178286942	AG09319	gingival:	n/a
39	chr5:178286875-178286925	SKMC	muscle:	n/a
40	chr5:178287112-178287162	NB4	blood:	n/a
41	chr5:178286920-178286970	PrEC	prostate:	n/a
42	chr5:178286735-178286785	HRCEpiC	kidney:	n/a
43	chr5:178291250-178291300	NHBE	bronchial:	n/a
44	chr5:178287767-178287817	ovcar-3	ovarian:	n/a
45	chr5:178288359-178288409	PANC-1	pancreas:	n/a
46	chr5:178287445-178287495	GM12878	blood:	n/a
47	chr5:178288625-178288675	SK-N-MC	brain:	n/a
48	chr5:178286626-178286676	Caco-2	colon:	n/a
49	chr5:178287445-178287495	HIPEpiC	eye:	n/a
50	chr5:178286857-178286907	AG04449	skin:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178157412..178158250-chr5:178286406..178286923,4	MCF-7	breast:
2	chr5:178157446..178157947-chr5:178286420..178286940,2	MCF-7	breast:
3	chr5:178152146..178155385-chr5:178293103..178294784,3	MCF-7	breast:
4	chr5:178286202..178288333-chr5:178295235..178296864,2	MCF-7	breast:
5	chr5:177640785..177642286-chr5:178288319..178291268,2	K562	blood:
6	chr5:178285646..178289279-chr5:178321547..178324884,4	MCF-7	breast:
7	chr5:178285911..178288443-chr5:178294689..178296630,2	K562	blood:
8	chr5:178290096..178292803-chr5:178294356..178296794,2	K562	blood:
9	chr5:178157230..178157844-chr5:178286636..178287441,3	MCF-7	breast:
10	chr5:178279881..178281408-chr5:178284466..178287127,2	MCF-7	breast:
11	chr5:178157243..178158078-chr5:178286943..178287443,2	MCF-7	breast:
12	chr5:178266086..178268148-chr5:178277968..178280958,2	MCF-7	breast:
13	chr5:178285700..178288538-chr5:178289208..178291375,4	MCF-7	breast:
14	chr5:178053391..178055177-chr5:178285758..178288394,2	MCF-7	breast:
15	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
16	chr5:178156014..178158845-chr5:178285994..178289826,5	MCF-7	breast:
17	chr5:178290096..178292803-chr5:178294356..178296794,2	K562	blood:
18	chr5:178154802..178159439-chr5:178284936..178288781,7	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF354B	TF binding region
ZNF354B	CpG island
ENSG00000178338	chromatin interactions
ENSG00000113240	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000198939	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000253725	chromatin interactions

Extended variants
information (count: 851 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189124715	chr5:178279655-178279656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs62393041	chr5:178279663-178279664	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs140472927	chr5:178279850-178279851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561413285	chr5:178279868-178279869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528272348	chr5:178279869-178279870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546850203	chr5:178279875-178279876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs13185338	chr5:178279883-178279884	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs571533189	chr5:178279904-178279905	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs143669004	chr5:178279921-178279922	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13168290	chr5:178279927-178279928	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs568844688	chr5:178279929-178279930	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs535912110	chr5:178279941-178279942	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554243487	chr5:178279950-178279951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566260136	chr5:178279969-178279970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374872558	chr5:178280000-178280001	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs28526638	chr5:178280025-178280026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553170308	chr5:178280026-178280027	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150243322	chr5:178280069-178280070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369583212	chr5:178280070-178280071	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181067392	chr5:178280111-178280112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs9716846	chr5:178280188-178280189	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs113936390	chr5:178280249-178280250	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs368516322	chr5:178280252-178280253	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544565573	chr5:178280253-178280254	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs550682270	chr5:178280258-178280259	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs398093917	chr5:178280260-178280261	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201911758	chr5:178280261-178280262	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377011477	chr5:178280265-178280266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12655480	chr5:178280271-178280272	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs112637606	chr5:178280306-178280307	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs12658098	chr5:178280334-178280335	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs139292998	chr5:178280380-178280381	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78354004	chr5:178280419-178280420	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576289129	chr5:178280442-178280443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532267021	chr5:178280482-178280483	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs386695535	chr5:178280485-178280486	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs62393042	chr5:178280487-178280488	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529673823	chr5:178280489-178280490	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12659592	chr5:178280499-178280500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs145828240	chr5:178280534-178280535	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533642432	chr5:178280546-178280547	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs62393043	chr5:178280560-178280561	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138739452	chr5:178280561-178280562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538907110	chr5:178280573-178280574	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115793351	chr5:178280582-178280583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552601877	chr5:178280598-178280599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545076678	chr5:178280654-178280655	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184353525	chr5:178280658-178280659	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536613855	chr5:178280734-178280735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs555026126	chr5:178280757-178280758	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178263600-178286400	Weak transcription	Right Atrium	heart
2	chr5:178266400-178281600	Weak transcription	Placenta	Placenta
3	chr5:178281400-178281600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178281400-178281600	Bivalent Enhancer	K562	blood
5	chr5:178281400-178281800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr5:178281400-178281800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:178281600-178281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:178281600-178281800	Enhancers	K562	blood
9	chr5:178281600-178282000	Enhancers	Placenta	Placenta
10	chr5:178281800-178282400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:178282000-178286400	Weak transcription	K562	blood
12	chr5:178282000-178286600	Weak transcription	Placenta	Placenta
13	chr5:178282400-178286600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:178284200-178286600	Weak transcription	HSMMtube	muscle
15	chr5:178285800-178286200	Enhancers	HepG2	liver
16	chr5:178285800-178286800	Flanking Active TSS	Dnd41	blood
17	chr5:178286000-178286200	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr5:178286000-178286600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr5:178286000-178287600	Active TSS	Rectal Mucosa Donor 31	rectum
20	chr5:178286000-178288400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr5:178286200-178286400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:178286200-178286400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:178286200-178286400	Enhancers	Primary T cells from cord blood	blood
24	chr5:178286200-178286400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr5:178286200-178286400	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr5:178286200-178286400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr5:178286200-178286400	Flanking Active TSS	HepG2	liver
28	chr5:178286200-178286400	Enhancers	HMEC	breast
29	chr5:178286200-178286400	Enhancers	HUVEC	blood vessel
30	chr5:178286200-178286600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:178286200-178286600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr5:178286200-178286600	Enhancers	Brain Cingulate Gyrus	brain
33	chr5:178286200-178286800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr5:178286200-178286800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr5:178286200-178287600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:178286200-178287600	Active TSS	Stomach Mucosa	stomach
37	chr5:178286200-178287600	Active TSS	A549	lung
38	chr5:178286200-178287800	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr5:178286400-178286600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:178286400-178286600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:178286400-178286600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:178286400-178286600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:178286400-178286600	Enhancers	Primary B cells from peripheral blood	blood
44	chr5:178286400-178286600	Active TSS	Primary T cells fromperipheralblood	blood
45	chr5:178286400-178286600	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr5:178286400-178286600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr5:178286400-178286600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:178286400-178286600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:178286400-178286600	Enhancers	Brain Substantia Nigra	brain
50	chr5:178286400-178286600	Enhancers	Fetal Intestine Large	intestine

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