Variant report

Variant	nsv832884
Chromosome Location	chr14:104610637-104665398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:73)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

No data

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:104630677..104633176-chr14:104635103..104637236,2	MCF-7	breast:
2	chr14:104609989..104612052-chr14:105021237..105023581,2	MCF-7	breast:
3	chr14:104623348..104624079-chr14:104760154..104761091,2	MCF-7	breast:
4	chr14:104649230..104653061-chr14:104657794..104660199,5	MCF-7	breast:
5	chr14:104612474..104614678-chr14:104620921..104622623,2	MCF-7	breast:
6	chr14:104646912..104648600-chr14:104679599..104681696,2	MCF-7	breast:
7	chr14:104617545..104619541-chr14:104760413..104762032,2	MCF-7	breast:
8	chr14:104630276..104632688-chr14:104639185..104641198,2	MCF-7	breast:
9	chr14:104650176..104652362-chr14:104808842..104810389,2	MCF-7	breast:
10	chr14:104644034..104647829-chr14:104648059..104652639,5	MCF-7	breast:
11	chr14:104628046..104630525-chr14:104634127..104635696,2	MCF-7	breast:
12	chr14:104607251..104609169-chr14:104611291..104612869,2	MCF-7	breast:
13	chr14:104611975..104614306-chr14:104614594..104616592,2	MCF-7	breast:
14	chr14:104637508..104640421-chr14:104649656..104651711,3	MCF-7	breast:
15	chr14:104602083..104606800-chr14:104649678..104656936,9	MCF-7	breast:
16	chr14:104637580..104639264-chr14:104654137..104656969,2	MCF-7	breast:
17	chr14:104648873..104651309-chr14:104652979..104655035,2	MCF-7	breast:
18	chr14:104648128..104650382-chr14:104654649..104656553,2	K562	blood:
19	chr14:104627021..104629659-chr14:104644533..104646486,2	MCF-7	breast:
20	chr14:104636638..104639934-chr14:104644485..104647895,3	MCF-7	breast:
21	chr14:104643343..104645021-chr14:104648909..104651142,2	K562	blood:
22	chr14:104655728..104658058-chr14:104665902..104667845,2	MCF-7	breast:
23	chr14:104603737..104606003-chr14:104636716..104639612,2	MCF-7	breast:
24	chr14:104603834..104608266-chr14:104611469..104617292,9	MCF-7	breast:
25	chr14:104611975..104614306-chr14:104614594..104616592,2	MCF-7	breast:
26	chr14:104643343..104645021-chr14:104648909..104651142,2	K562	blood:
27	chr14:104570906..104573518-chr14:104661055..104663991,2	MCF-7	breast:
28	chr14:104620973..104623022-chr14:104627568..104629644,2	MCF-7	breast:
29	chr14:104637508..104640421-chr14:104649656..104651711,3	MCF-7	breast:
30	chr14:104632447..104634396-chr14:104650392..104653194,2	K562	blood:
31	chr14:104637815..104640571-chr14:104677890..104680782,2	MCF-7	breast:
32	chr14:104654764..104655392-chr14:104812527..104813058,2	MCF-7	breast:
33	chr14:104630276..104632688-chr14:104639185..104641198,2	MCF-7	breast:
34	chr14:104652967..104655075-chr14:105050050..105051684,2	MCF-7	breast:
35	chr14:104627113..104628867-chr14:104628876..104631765,2	MCF-7	breast:
36	chr14:104625626..104628004-chr14:104636602..104638636,2	MCF-7	breast:
37	chr14:104649534..104651729-chr14:104660798..104662472,2	MCF-7	breast:
38	chr14:104641001..104643795-chr14:104659198..104661496,2	MCF-7	breast:
39	chr14:104620973..104623022-chr14:104627568..104629644,2	MCF-7	breast:
40	chr14:104627113..104628867-chr14:104628876..104631765,2	MCF-7	breast:
41	chr14:104604927..104606728-chr14:104610175..104612762,2	MCF-7	breast:
42	chr14:104632447..104634396-chr14:104650392..104653194,2	K562	blood:
43	chr14:104649570..104650550-chr3:64449241..64449782,2	MCF-7	breast:
44	chr14:104651259..104651765-chr14:104760560..104761404,2	MCF-7	breast:
45	chr14:104612474..104614678-chr14:104620921..104622623,2	MCF-7	breast:
46	chr14:104633441..104636247-chr14:104642417..104644360,2	MCF-7	breast:
47	chr14:104610504..104612427-chr14:105051437..105054279,2	MCF-7	breast:
48	chr14:104644824..104647219-chr14:104651116..104653195,2	K562	blood:
49	chr14:104654038..104657382-chr14:104659420..104664106,7	MCF-7	breast:
50	chr14:104654038..104657382-chr14:104659420..104664106,7	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPG-3	chr14:104632709-104632824	l_1077_chr14:104630225-104633148_lung
2	lnc-ASPG-3	chr14:104630226-104630291	l_1077_chr14:104630225-104633148_lung
3	lnc-ASPG-3	chr14:104632922-104633148	l_1077_chr14:104630225-104633148_lung
4	lnc-ASPG-3	chr14:104630871-104631102	l_1077_chr14:104630225-104633148_lung

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF26A	hsa-miR-124-3p	chr14:104646343-104646364
2	KIF26A	hsa-miR-124-3p	chr14:104646357-104646363

Variant related genes	Relation type
ENSG00000258748	chromatin interactions
ENSG00000256050	chromatin interactions
ENSG00000166183	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000207568	chromatin interactions

Extended variants
information (count: 3147 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3147 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370834319	chr14:104610659-104610660	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs569910602	chr14:104610691-104610692	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374352434	chr14:104610728-104610729	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535845788	chr14:104610818-104610819	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs10142824	chr14:104610852-104610853	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs185752156	chr14:104610922-104610923	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs28529830	chr14:104610937-104610938	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138068694	chr14:104610945-104610946	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189310645	chr14:104610958-104610959	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565332125	chr14:104611013-104611014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369511317	chr14:104611062-104611063	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143549504	chr14:104611119-104611120	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs180898439	chr14:104611130-104611131	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573527213	chr14:104611132-104611133	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147157572	chr14:104611161-104611162	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183742540	chr14:104611173-104611174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534109883	chr14:104611195-104611196	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73358270	chr14:104611196-104611197	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564382667	chr14:104611243-104611244	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs72714966	chr14:104611260-104611261	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530393803	chr14:104611320-104611321	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs11626880	chr14:104611326-104611327	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566362417	chr14:104611350-104611351	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538590590	chr14:104611388-104611389	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35439917	chr14:104611432-104611433	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535163208	chr14:104611442-104611443	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551913361	chr14:104611467-104611468	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571420171	chr14:104611483-104611484	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs562821722	chr14:104611500-104611501	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs188802007	chr14:104611527-104611528	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs556939335	chr14:104611544-104611545	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113175982	chr14:104611547-104611548	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs573911570	chr14:104611549-104611550	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73358276	chr14:104611570-104611571	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552981629	chr14:104611586-104611587	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs572597336	chr14:104611598-104611599	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79856329	chr14:104611601-104611602	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564641227	chr14:104611602-104611603	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568933395	chr14:104611619-104611620	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544011510	chr14:104611652-104611653	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563814355	chr14:104611680-104611681	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529637292	chr14:104611700-104611701	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs35956368	chr14:104611761-104611762	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12887046	chr14:104611780-104611781	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528497574	chr14:104611787-104611788	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551867832	chr14:104611791-104611792	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571781977	chr14:104611828-104611829	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530943695	chr14:104611831-104611832	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181193613	chr14:104611853-104611854	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148808752	chr14:104611885-104611886	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104605800-104615400	Weak transcription	Gastric	stomach
2	chr14:104606000-104613800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:104606400-104615200	Weak transcription	Left Ventricle	heart
4	chr14:104606800-104614000	Weak transcription	Colonic Mucosa	Colon
5	chr14:104606800-104615400	Weak transcription	Right Atrium	heart
6	chr14:104607000-104613600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr14:104607000-104613800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:104607000-104614200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr14:104607000-104614400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:104607000-104614400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr14:104607000-104616200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr14:104607200-104611600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
13	chr14:104607200-104614200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr14:104607400-104613800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:104607600-104611200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:104607800-104611000	Weak transcription	Fetal Lung	lung
17	chr14:104607800-104613600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:104608400-104611600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr14:104609200-104615800	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr14:104609400-104611600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr14:104609600-104611600	Genic enhancers	Fetal Stomach	stomach
22	chr14:104609800-104610800	Enhancers	Right Ventricle	heart
23	chr14:104609800-104612800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr14:104609800-104615200	Weak transcription	Fetal Intestine Small	intestine
25	chr14:104610000-104611400	Weak transcription	Brain Germinal Matrix	brain
26	chr14:104610000-104613200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:104610400-104612400	Weak transcription	Fetal Brain Male	brain
28	chr14:104610400-104618000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:104610600-104611400	Weak transcription	Fetal Brain Female	brain
30	chr14:104610600-104617600	Enhancers	Spleen	Spleen
31	chr14:104610800-104611600	Weak transcription	Right Ventricle	heart
32	chr14:104611000-104611600	Enhancers	Fetal Lung	lung
33	chr14:104611200-104611400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:104611200-104611600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
35	chr14:104611400-104611800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:104611400-104611800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:104611400-104611800	Genic enhancers	Fetal Brain Female	brain
38	chr14:104611400-104617000	Enhancers	Brain Germinal Matrix	brain
39	chr14:104611400-104619200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr14:104611600-104612000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:104611600-104612200	Bivalent Enhancer	Fetal Stomach	stomach
42	chr14:104611600-104612200	Bivalent Enhancer	Right Ventricle	heart
43	chr14:104611600-104613400	Weak transcription	Fetal Lung	lung
44	chr14:104611600-104614200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr14:104611600-104618000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr14:104611800-104612000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:104611800-104612600	Enhancers	Fetal Brain Female	brain
48	chr14:104612000-104612200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:104612000-104613600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:104612000-104613600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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