Variant report

Variant	nsv883262
Chromosome Location	chr5:178861350-178944407
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	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
4	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr5:178867642-178867915	K562	blood:	n/a	chr5:178867741-178867750 chr5:178867742-178867751 chr5:178867742-178867751 chr5:178867743-178867752 chr5:178867736-178867757 chr5:178867740-178867753
6	BHLHE40	chr5:178868515-178868770	K562	blood:	n/a	chr5:178868635-178868644 chr5:178868636-178868645 chr5:178868634-178868647 chr5:178868630-178868651 chr5:178868636-178868645 chr5:178868637-178868646
7	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
8	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
9	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:178918772-178918946	K562	blood:	n/a	chr5:178918811-178918822
11	CEBPB	chr5:178882280-178882457	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:178918660-178918869	IMR90	lung:	n/a	chr5:178918811-178918822
13	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
14	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:178921088-178921413	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:178918785-178918864	HepG2	liver:	n/a	chr5:178918811-178918822
18	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:178901904-178902149	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
22	CEBPB	chr5:178901859-178902134	K562	blood:	n/a	n/a
23	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:178920783-178920906	K562	blood:	n/a	n/a
25	CEBPB	chr5:178898849-178899101	K562	blood:	n/a	n/a
26	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:178901917-178902069	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:178882230-178882319	A549	lung:	n/a	n/a
33	CEBPB	chr5:178913744-178914042	IMR90	lung:	n/a	chr5:178913860-178913871
34	CTCF	chr5:178921120-178921270	GM12867	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
35	CTCF	chr5:178921160-178921310	NHEK	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
36	CTCF	chr5:178921160-178921310	HEK293	kidney:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
37	CTCF	chr5:178921160-178921310	HEEpiC	esophagus:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
38	CTCF	chr5:178921180-178921330	GM12869	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
39	CTCF	chr5:178921140-178921290	AoAF	blood vessel:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
40	CTCF	chr5:178921985-178922175	GM19239	blood:	n/a	n/a
41	CTCF	chr5:178923000-178923150	WERI-Rb-1	eye:	n/a	chr5:178923029-178923037
42	CTCF	chr5:178922980-178923130	BE2_C	brain:	n/a	chr5:178923029-178923037
43	CTCF	chr5:178921079-178921382	Spleen_OC	spleen:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
44	CTCF	chr5:178921237-178921339	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:178921130-178921307	SK-N-SH_RA	brain:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
46	CTCF	chr5:178921180-178921330	HAc	cerebellar:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
47	CTCF	chr5:178922834-178923327	MCF-7	breast:	n/a	chr5:178923029-178923037
48	CTCF	chr5:178921160-178921310	HepG2	liver:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
49	CTCF	chr5:178921140-178921290	BJ	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
50	CTCF	chr5:178921240-178921346	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178902699-178902749	AG09319	gingival:	n/a
2	chr5:178902699-178902749	AG09319	gingival:	n/a
3	chr5:178902699-178902749	Hela-S3	cervix:	n/a
4	chr5:178903087-178903137	HCT-116	colon:	n/a
5	chr5:178902790-178902840	T-47D	breast:	n/a
6	chr5:178899812-178899862	T-47D	breast:	n/a
7	chr5:178903087-178903137	MCF-7	breast:	n/a
8	chr5:178882605-178882655	SK-N-SH	brain:	n/a
9	chr5:178902699-178902749	H1-hESC	embryonic stem cell:	embryo
10	chr5:178902699-178902749	BJ	skin:	n/a
11	chr5:178899789-178899839	ovcar-3	ovarian:	n/a
12	chr5:178913683-178913733	NHDF-neo	bronchial:	n/a
13	chr5:178902699-178902749	MCF10A-Er-Src	breast:	n/a
14	chr5:178902699-178902749	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:178882763-178882813	AG09319	gingival:	n/a
16	chr5:178882763-178882813	AG09309	skin:	n/a
17	chr5:178902956-178903006	MCF-7	breast:	n/a
18	chr5:178899789-178899839	ProgFib	skin:	n/a
19	chr5:178913683-178913733	U87	brain:	n/a
20	chr5:178903057-178903107	HepG2	liver:	n/a
21	chr5:178902699-178902749	PFSK-1	brain:	n/a
22	chr5:178899789-178899839	T-47D	breast:	n/a
23	chr5:178899850-178899900	GM12892	blood:	n/a
24	chr5:178913683-178913733	AG09319	gingival:	n/a
25	chr5:178903087-178903137	HNPCEpiC	eye:	n/a
26	chr5:178902699-178902749	MCF-7	breast:	n/a
27	chr5:178903057-178903107	MCF10A-Er-Src	breast:	n/a
28	chr5:178903057-178903107	SK-N-MC	brain:	n/a
29	chr5:178913683-178913733	MCF10A-Er-Src	breast:	n/a
30	chr5:178882605-178882655	NHBE	bronchial:	n/a
31	chr5:178902790-178902840	HAEpiC	amniotic membrane:	n/a
32	chr5:178902699-178902749	HAEpiC	amniotic membrane:	n/a
33	chr5:178902699-178902749	HCT-116	colon:	n/a
34	chr5:178902699-178902749	PANC-1	pancreas:	n/a
35	chr5:178902956-178903006	GM06990	blood:	n/a
36	chr5:178903087-178903137	HUVEC	blood vessel:	n/a
37	chr5:178902956-178903006	AG04450	lung:	fetal
38	chr5:178882605-178882655	SKMC	muscle:	n/a
39	chr5:178899850-178899900	ovcar-3	ovarian:	n/a
40	chr5:178902699-178902749	HUVEC	blood vessel:	n/a
41	chr5:178902956-178903006	HepG2	liver:	n/a
42	chr5:178899789-178899839	AG04450	lung:	fetal
43	chr5:178902699-178902749	HCM	heart:	n/a
44	chr5:178882763-178882813	U87	brain:	n/a
45	chr5:178903057-178903107	Jurkat	blood:	n/a
46	chr5:178899789-178899839	ECC-1	luminal epithelium:	n/a
47	chr5:178913683-178913733	HRPEpiC	eye:	n/a
48	chr5:178903057-178903107	CMK	blood:	n/a
49	chr5:178902956-178903006	GM19239	blood:	n/a
50	chr5:178899850-178899900	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
2	chr5:178882272..178884920-chr5:179049238..179052060,2	K562	blood:
3	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
4	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
5	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
6	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
7	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:
8	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
9	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
10	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
11	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
12	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
13	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
14	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
15	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
16	chr5:178871548..178873217-chr5:178880850..178883062,2	MCF-7	breast:
17	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
18	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
19	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
20	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS2-2	chr5:178893834-178894126	NONHSAT105584
2	lnc-HNRNPH1-3	chr5:178942465-178942580	ENSG00000253652
3	lnc-RUFY1-1	chr5:178882416-178882818	XLOC_004674
4	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652
5	lnc-RUFY1-1	chr5:178882939-178883096	XLOC_004674

Variant related genes	Relation type
ENSG00000250674	TF binding region
ENSG00000253652	TF binding region
RN7SL71P	TF binding region
ENSG00000250674	CpG island
ENSG00000253652	CpG island
RN7SL71P	CpG island
ENSG00000264205	chromatin interactions
ENSG00000250674	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000176783	chromatin interactions

Extended variants
information (count: 3787 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3787 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7714843	chr5:178861350-178861351	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558909356	chr5:178861381-178861382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577348244	chr5:178861400-178861401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73808436	chr5:178861412-178861413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73808437	chr5:178861451-178861452	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs3987735	chr5:178861485-178861486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374870726	chr5:178861486-178861487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574787525	chr5:178861508-178861509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541824610	chr5:178861582-178861583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74533268	chr5:178861585-178861586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565167980	chr5:178861587-178861588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191540907	chr5:178861605-178861606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545863178	chr5:178861606-178861607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7714961	chr5:178861614-178861615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7714972	chr5:178861641-178861642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375627288	chr5:178861676-178861677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111698306	chr5:178861683-178861684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112487293	chr5:178861703-178861704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112676816	chr5:178861728-178861729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12653425	chr5:178861732-178861733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs565654811	chr5:178861743-178861744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539570072	chr5:178861744-178861745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35404276	chr5:178861746-178861747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557819428	chr5:178861772-178861773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570999097	chr5:178861773-178861774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538431350	chr5:178861774-178861775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556435053	chr5:178861784-178861785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574801278	chr5:178861786-178861787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374092964	chr5:178861796-178861797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192548117	chr5:178861797-178861798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113572567	chr5:178861802-178861803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112141936	chr5:178861805-178861806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181825872	chr5:178861825-178861826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375538589	chr5:178861828-178861829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186889089	chr5:178861829-178861830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149918768	chr5:178861875-178861876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546389074	chr5:178861877-178861878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145253771	chr5:178861879-178861880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7732728	chr5:178861889-178861890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs532949744	chr5:178861977-178861978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73808438	chr5:178862021-178862022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575465789	chr5:178862036-178862037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538846627	chr5:178862076-178862077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78785939	chr5:178862125-178862126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375001055	chr5:178862143-178862144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142478518	chr5:178862173-178862174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568286543	chr5:178862177-178862178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146505227	chr5:178862178-178862179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554026816	chr5:178862187-178862188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73808439	chr5:178862222-178862223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178860400-178864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:178862600-178862800	Enhancers	Fetal Lung	lung
3	chr5:178862800-178863000	Bivalent Enhancer	Right Ventricle	heart
4	chr5:178862800-178864200	Weak transcription	Fetal Lung	lung
5	chr5:178863000-178866200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:178863000-178866600	Enhancers	Spleen	Spleen
7	chr5:178863200-178863400	Enhancers	Placenta	Placenta
8	chr5:178863200-178863600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr5:178863400-178863800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:178863400-178864000	Weak transcription	Placenta	Placenta
11	chr5:178863600-178867200	Bivalent Enhancer	Fetal Stomach	stomach
12	chr5:178863800-178864200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:178864000-178866400	Enhancers	Placenta	Placenta
14	chr5:178864200-178864800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:178864200-178865000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:178864200-178865200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:178864200-178865200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr5:178864200-178865400	Enhancers	Fetal Muscle Leg	muscle
19	chr5:178864200-178867400	Enhancers	Fetal Lung	lung
20	chr5:178864400-178865600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:178864400-178865800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr5:178864400-178866200	Enhancers	Ovary	ovary
23	chr5:178864600-178864800	Enhancers	Fetal Intestine Small	intestine
24	chr5:178864600-178866000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:178864800-178865000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
26	chr5:178864800-178865800	Enhancers	Placenta Amnion	Placenta Amnion
27	chr5:178865000-178866600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:178865000-178867600	Enhancers	Fetal Brain Male	brain
29	chr5:178865400-178867200	Enhancers	Fetal Brain Female	brain
30	chr5:178865600-178867600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:178866000-178866200	Enhancers	Fetal Muscle Leg	muscle
32	chr5:178866800-178867000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr5:178867600-178867800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:178872600-178873800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:178877400-178880200	Enhancers	Brain Germinal Matrix	brain
36	chr5:178877600-178879600	Enhancers	Fetal Brain Female	brain
37	chr5:178877600-178880000	Enhancers	Fetal Brain Male	brain
38	chr5:178878400-178879200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr5:178878400-178879200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr5:178878400-178879400	Enhancers	Brain Substantia Nigra	brain
41	chr5:178878600-178879000	Enhancers	Brain Angular Gyrus	brain
42	chr5:178878800-178879000	Bivalent Enhancer	Fetal Stomach	stomach
43	chr5:178878800-178879200	Enhancers	Brain Cingulate Gyrus	brain
44	chr5:178878800-178879800	ZNF genes & repeats	Spleen	Spleen
45	chr5:178879800-178880200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:178880200-178880600	Weak transcription	Spleen	Spleen
47	chr5:178880200-178881600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:178881000-178881200	Enhancers	Fetal Stomach	stomach
49	chr5:178881200-178882600	Weak transcription	Fetal Stomach	stomach
50	chr5:178881400-178881600	Enhancers	Ovary	ovary

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