Variant report

Variant	nsv883265
Chromosome Location	chr5:178897725-178936722
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	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
4	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:178898849-178899101	K562	blood:	n/a	n/a
6	CEBPB	chr5:178901904-178902149	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:178918772-178918946	K562	blood:	n/a	chr5:178918811-178918822
8	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
9	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr5:178901859-178902134	K562	blood:	n/a	n/a
11	CEBPB	chr5:178918660-178918869	IMR90	lung:	n/a	chr5:178918811-178918822
12	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:178920783-178920906	K562	blood:	n/a	n/a
16	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:178913744-178914042	IMR90	lung:	n/a	chr5:178913860-178913871
18	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
20	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:178901917-178902069	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:178918785-178918864	HepG2	liver:	n/a	chr5:178918811-178918822
23	CEBPB	chr5:178921088-178921413	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr5:178921163-178921380	NHEK	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
29	CTCF	chr5:178921119-178921369	T-47D	breast:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
30	CTCF	chr5:178922960-178923110	HMEC	breast:	n/a	chr5:178923029-178923037
31	CTCF	chr5:178921180-178921330	SK-N-SH_RA	brain:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
32	CTCF	chr5:178921120-178921270	HL-60	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
33	CTCF	chr5:178922975-178923173	Hela-S3	cervix:	n/a	chr5:178923029-178923037
34	CTCF	chr5:178921179-178921353	ProgFib	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
35	CTCF	chr5:178921160-178921310	SAEC	small airway:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
36	CTCF	chr5:178921051-178921293	A549	lung:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
37	CTCF	chr5:178921160-178921310	HMF	breast:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
38	CTCF	chr5:178921089-178921358	GM13977	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
39	CTCF	chr5:178920993-178921351	T-47D	breast:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
40	CTCF	chr5:178921180-178921330	HVMF	connective:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
41	CTCF	chr5:178921180-178921330	GM12865	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
42	CTCF	chr5:178921183-178921347	GM19240	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
43	CTCF	chr5:178921120-178921270	SAEC	small airway:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
44	CTCF	chr5:178921160-178921310	GM12869	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
45	CTCF	chr5:178923100-178923250	WI-38	lung:	n/a	n/a
46	CTCF	chr5:178922880-178923030	GM06990	blood:	n/a	n/a
47	CTCF	chr5:178923000-178923150	WERI-Rb-1	eye:	n/a	chr5:178923029-178923037
48	CTCF	chr5:178921008-178921335	HepG2	liver:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
49	CTCF	chr5:178921200-178921350	GM12872	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
50	CTCF	chr5:178921160-178921310	GM12870	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178903057-178903107	T-47D	breast:	n/a
2	chr5:178902956-178903006	GM12891	blood:	n/a
3	chr5:178903087-178903137	Caco-2	colon:	n/a
4	chr5:178913683-178913733	LNCaP	prostate:	n/a
5	chr5:178899850-178899900	BE2_C	brain:	n/a
6	chr5:178902699-178902749	Jurkat	blood:	n/a
7	chr5:178899789-178899839	ECC-1	luminal epithelium:	n/a
8	chr5:178913683-178913733	IMR90	lung:	fetal
9	chr5:178902699-178902749	GM19239	blood:	n/a
10	chr5:178902956-178903006	HL-60	blood:	n/a
11	chr5:178903087-178903137	BJ	skin:	n/a
12	chr5:178902699-178902749	HAEpiC	amniotic membrane:	n/a
13	chr5:178899812-178899862	GM12891	blood:	n/a
14	chr5:178903057-178903107	HMEC	breast:	n/a
15	chr5:178899812-178899862	HCT-116	colon:	n/a
16	chr5:178902699-178902749	K562	blood:	n/a
17	chr5:178902956-178903006	HRPEpiC	eye:	n/a
18	chr5:178902790-178902840	HCM	heart:	n/a
19	chr5:178902699-178902749	ovcar-3	ovarian:	n/a
20	chr5:178903057-178903107	HRE	kidney:	n/a
21	chr5:178902956-178903006	HEK293	kidney:	embryo
22	chr5:178902790-178902840	NH-A	brain:	n/a
23	chr5:178899812-178899862	Caco-2	colon:	n/a
24	chr5:178899789-178899839	HEK293	kidney:	embryo
25	chr5:178913683-178913733	PANC-1	pancreas:	n/a
26	chr5:178902699-178902749	ECC-1	luminal epithelium:	n/a
27	chr5:178902956-178903006	Hepatocyte	liver:	n/a
28	chr5:178902956-178903006	AG09309	skin:	n/a
29	chr5:178899812-178899862	HAEpiC	amniotic membrane:	n/a
30	chr5:178902790-178902840	NT2-D1	testis:	n/a
31	chr5:178902956-178903006	SKMC	muscle:	n/a
32	chr5:178902790-178902840	H1-hESC	embryonic stem cell:	embryo
33	chr5:178899789-178899839	SK-N-MC	brain:	n/a
34	chr5:178902956-178903006	H1-hESC	embryonic stem cell:	embryo
35	chr5:178899789-178899839	HRCEpiC	kidney:	n/a
36	chr5:178902956-178903006	HMEC	breast:	n/a
37	chr5:178902956-178903006	HEEpiC	esophagus:	n/a
38	chr5:178899850-178899900	ovcar-3	ovarian:	n/a
39	chr5:178899850-178899900	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:178899789-178899839	BE2_C	brain:	n/a
41	chr5:178899850-178899900	HCF	heart:	n/a
42	chr5:178913683-178913733	HepG2	liver:	n/a
43	chr5:178902956-178903006	AG04449	skin:	fetal
44	chr5:178913683-178913733	PrEC	prostate:	n/a
45	chr5:178899812-178899862	IMR90	lung:	fetal
46	chr5:178899789-178899839	PrEC	prostate:	n/a
47	chr5:178913683-178913733	H1-hESC	embryonic stem cell:	embryo
48	chr5:178903057-178903107	AG09309	skin:	n/a
49	chr5:178899812-178899862	HRPEpiC	eye:	n/a
50	chr5:178913683-178913733	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
2	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
3	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
4	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
5	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
6	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
7	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
8	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:
9	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
10	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
11	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
12	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
13	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
14	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
15	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
16	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
17	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
18	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652

Variant related genes	Relation type
RN7SL71P	TF binding region
RN7SL71P	CpG island
ENSG00000264205	chromatin interactions
ENSG00000176783	chromatin interactions

Extended variants
information (count: 1887 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1887 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4700827	chr5:178897725-178897726	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561868623	chr5:178897727-178897728	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs4700828	chr5:178897747-178897748	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs193227930	chr5:178897750-178897751	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185194486	chr5:178897807-178897808	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567567699	chr5:178897830-178897831	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142447101	chr5:178897851-178897852	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369345921	chr5:178897876-178897877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569708066	chr5:178897877-178897878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10668637	chr5:178897913-178897914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538087150	chr5:178897962-178897963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550337260	chr5:178897970-178897971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs75793779	chr5:178898000-178898001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377671992	chr5:178898014-178898015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190093104	chr5:178898042-178898043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536157799	chr5:178898046-178898047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200976070	chr5:178898055-178898056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545958708	chr5:178898056-178898057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554463244	chr5:178898058-178898059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572487926	chr5:178898060-178898061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201970441	chr5:178898061-178898062	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539814152	chr5:178898063-178898064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369536654	chr5:178898089-178898090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181553779	chr5:178898117-178898118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576466580	chr5:178898134-178898135	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543292758	chr5:178898217-178898218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530477663	chr5:178898225-178898226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7736974	chr5:178898259-178898260	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs540938307	chr5:178898302-178898303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559189358	chr5:178898303-178898304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34811414	chr5:178898314-178898315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113839084	chr5:178898329-178898330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7700470	chr5:178898330-178898331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7723903	chr5:178898342-178898343	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546817171	chr5:178898345-178898346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567037078	chr5:178898351-178898352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188582733	chr5:178898360-178898361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7704302	chr5:178898380-178898381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58569602	chr5:178898381-178898382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs552259110	chr5:178898402-178898403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180989643	chr5:178898405-178898406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548131061	chr5:178898410-178898411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs386695630	chr5:178898412-178898413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7703214	chr5:178898413-178898414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558123033	chr5:178898436-178898437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569505539	chr5:178898441-178898442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7723752	chr5:178898458-178898459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568600221	chr5:178898463-178898464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77689327	chr5:178898488-178898489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs70997690	chr5:178898502-178898503	Weak transcription	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178897400-178897800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:178897600-178899600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:178897800-178902200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:178899600-178900000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178899800-178900000	Enhancers	Brain Germinal Matrix	brain
6	chr5:178899800-178900000	Enhancers	Placenta	Placenta
7	chr5:178899800-178900000	Enhancers	Pancreas	Pancrea
8	chr5:178900000-178902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:178900000-178902200	Weak transcription	Placenta	Placenta
10	chr5:178900200-178901400	Weak transcription	Brain Germinal Matrix	brain
11	chr5:178900800-178902200	Enhancers	Fetal Lung	lung
12	chr5:178901400-178903200	Enhancers	Brain Germinal Matrix	brain
13	chr5:178901800-178902800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:178901800-178903200	Enhancers	Fetal Brain Male	brain
15	chr5:178902000-178902400	Enhancers	Primary hematopoietic stem cells	blood
16	chr5:178902000-178902800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr5:178902000-178902800	Enhancers	Fetal Brain Female	brain
18	chr5:178902000-178902800	Enhancers	HSMMtube	muscle
19	chr5:178902000-178903200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr5:178902000-178903200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:178902000-178903400	Enhancers	Fetal Kidney	kidney
22	chr5:178902200-178902400	Bivalent Enhancer	Brain Angular Gyrus	brain
23	chr5:178902200-178902600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:178902200-178902600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr5:178902200-178902600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:178902200-178902600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr5:178902200-178902600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr5:178902200-178902600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr5:178902200-178902600	Flanking Active TSS	Fetal Lung	lung
30	chr5:178902200-178902600	Enhancers	Fetal Muscle Leg	muscle
31	chr5:178902200-178902600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr5:178902200-178902800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:178902200-178902800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr5:178902200-178902800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:178902200-178902800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr5:178902200-178902800	Enhancers	Placenta	Placenta
37	chr5:178902200-178902800	Enhancers	Fetal Stomach	stomach
38	chr5:178902200-178902800	Enhancers	Spleen	Spleen
39	chr5:178902200-178903200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:178902200-178903200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:178902400-178902800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:178902400-178902800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:178902600-178903200	Enhancers	Fetal Lung	lung
44	chr5:178902800-178905200	Weak transcription	Spleen	Spleen
45	chr5:178902800-178918000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:178903200-178911600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:178905200-178905800	Enhancers	Spleen	Spleen
48	chr5:178905800-178908800	Weak transcription	Spleen	Spleen
49	chr5:178908800-178910000	Enhancers	Spleen	Spleen
50	chr5:178909200-178909800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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