Variant report

Variant	esv15328
Chromosome Location	chr14:35605540-35614541
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	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
3	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
4	CEBPB	chr14:35612279-35612564	HepG2	liver:	n/a	chr14:35612414-35612425
5	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:35613295-35613593	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:35612292-35612467	HepG2	liver:	n/a	chr14:35612414-35612425
8	CHD2	chr14:35613402-35613558	GM12878	blood:	n/a	n/a
9	CTCF	chr14:35609977-35610231	Pancreas_OC	pancreas:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
10	CTCF	chr14:35609900-35610050	AG09309	skin:	n/a	n/a
11	CTCF	chr14:35609735-35610610	SK-N-SH	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
12	CTCF	chr14:35610049-35610215	A549	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
13	CTCF	chr14:35610000-35610150	HEEpiC	esophagus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
14	CTCF	chr14:35610020-35610170	AoAF	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
15	CTCF	chr14:35610060-35610210	GM12864	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
16	CTCF	chr14:35610040-35610190	HL-60	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
17	CTCF	chr14:35610042-35610185	SK-N-SH_RA	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
18	CTCF	chr14:35610000-35610150	NHDF-neo	bronchial:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
19	CTCF	chr14:35609980-35610130	Hela-S3	cervix:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
20	CTCF	chr14:35610043-35610153	GM10248	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
21	CTCF	chr14:35609921-35610231	H1-hESC	embryonic stem cell:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
22	CTCF	chr14:35610040-35610190	WI-38	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
23	CTCF	chr14:35610060-35610210	HCM	heart:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
24	CTCF	chr14:35610004-35610180	A549	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
25	CTCF	chr14:35610040-35610190	GM06990	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
26	CTCF	chr14:35609700-35609850	HMEC	breast:	n/a	n/a
27	CTCF	chr14:35609280-35609430	AG10803	skin:	n/a	n/a
28	CTCF	chr14:35609980-35610130	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
29	CTCF	chr14:35610040-35610176	LNCaP	prostate:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
30	CTCF	chr14:35610040-35610190	GM12878	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
31	CTCF	chr14:35610000-35610150	HPF	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
32	CTCF	chr14:35610039-35610198	GM13977	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
33	CTCF	chr14:35610018-35610210	Kidney_OC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
34	CTCF	chr14:35610040-35610190	GM12801	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
35	CTCF	chr14:35610000-35610150	HRE	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
36	CTCF	chr14:35609963-35610210	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
37	CTCF	chr14:35610029-35610031	LNCaP	prostate:	n/a	n/a
38	CTCF	chr14:35609960-35610110	HMEC	breast:	n/a	n/a
39	CTCF	chr14:35609857-35610436	IMR90	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
40	CTCF	chr14:35610082-35610179	LNCaP	prostate:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
41	CTCF	chr14:35610040-35610190	HPAF	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
42	CTCF	chr14:35610004-35610248	Medullo	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
43	CTCF	chr14:35610031-35610194	GM12878	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
44	CTCF	chr14:35610040-35610190	RPTEC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
45	CTCF	chr14:35609980-35610130	AG04449	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
46	CTCF	chr14:35609950-35610327	HCT-116	colon:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
47	CTCF	chr14:35610040-35610190	HCPEpiC	choroid plexus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
48	CTCF	chr14:35610020-35610170	HVMF	connective:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
49	CTCF	chr14:35609980-35610130	HCPEpiC	choroid plexus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
50	CTCF	chr14:35609980-35610130	GM12864	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129

No.	Distal block	Cell Line	Cell type
1	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
2	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
3	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
4	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
5	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
6	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
7	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
8	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
9	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
10	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
11	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366

Variant related genes	Relation type
ENSG00000241052	TF binding region
ENSG00000100906	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000100890	chromatin interactions

Extended variants
information (count: 305 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540810935	chr14:35605566-35605567	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs35468265	chr14:35605567-35605568	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs202181058	chr14:35605571-35605572	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs200188288	chr14:35605577-35605578	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs368023807	chr14:35605578-35605579	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs186934052	chr14:35605582-35605583	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs542986986	chr14:35605588-35605589	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs563257138	chr14:35605601-35605602	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs200990493	chr14:35605629-35605630	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs532233118	chr14:35605658-35605659	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs543190887	chr14:35605667-35605668	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552350645	chr14:35605675-35605676	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs561351944	chr14:35605679-35605680	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs148856694	chr14:35605711-35605712	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs528277870	chr14:35605741-35605742	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs548426907	chr14:35605743-35605744	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs531956112	chr14:35605755-35605756	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568542123	chr14:35605760-35605761	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs191398104	chr14:35605800-35605801	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs112214339	chr14:35605803-35605804	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs571168027	chr14:35605827-35605828	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs539794072	chr14:35605832-35605833	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs553623359	chr14:35605859-35605860	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs202215277	chr14:35605868-35605869	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs4981267	chr14:35605876-35605877	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs137919771	chr14:35605914-35605915	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs554265992	chr14:35605924-35605925	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs143724145	chr14:35606006-35606007	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs201410697	chr14:35606011-35606012	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs4981268	chr14:35606016-35606017	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532504808	chr14:35606029-35606030	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs562896474	chr14:35606127-35606128	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs185691925	chr14:35606281-35606282	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs190215757	chr14:35606312-35606313	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs193167734	chr14:35606436-35606437	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs145216150	chr14:35606478-35606479	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs185047741	chr14:35606486-35606487	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs147230667	chr14:35606567-35606568	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs562175117	chr14:35606574-35606575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs567009460	chr14:35606594-35606595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs148240124	chr14:35606627-35606628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs551095008	chr14:35606633-35606634	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs370691027	chr14:35606660-35606661	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs28462285	chr14:35606810-35606811	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188852318	chr14:35606822-35606823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs141276504	chr14:35606832-35606833	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs548341393	chr14:35606894-35606895	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs150775307	chr14:35606930-35606931	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs535687553	chr14:35607014-35607015	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs368330596	chr14:35607064-35607065	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
2	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
5	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
6	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr14:35593200-35625200	Weak transcription	NH-A	brain
8	chr14:35593200-35625600	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:35593200-35627800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr14:35593200-35635400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr14:35593400-35613200	Weak transcription	Osteobl	bone
12	chr14:35593400-35617200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr14:35594000-35615800	Weak transcription	HUVEC	blood vessel
14	chr14:35594400-35629000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr14:35594600-35609600	Weak transcription	Colonic Mucosa	Colon
16	chr14:35595200-35613200	Weak transcription	K562	blood
17	chr14:35596000-35623600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr14:35597400-35625000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr14:35597600-35625000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr14:35597800-35615400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:35598000-35609800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:35599400-35607200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:35600400-35605600	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr14:35601400-35606000	Strong transcription	Thymus	Thymus
25	chr14:35601400-35607600	Strong transcription	Fetal Muscle Leg	muscle
26	chr14:35601400-35609200	Strong transcription	Fetal Thymus	thymus
27	chr14:35601600-35605600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:35601600-35607400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:35601600-35609600	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr14:35602000-35606600	Strong transcription	Primary T cells from cord blood	blood
31	chr14:35602000-35609600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr14:35602400-35609200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:35602800-35605600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr14:35602800-35606000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:35603000-35605600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:35603000-35607400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr14:35603000-35609400	Strong transcription	HepG2	liver
38	chr14:35603000-35625200	Weak transcription	HSMM	muscle
39	chr14:35603200-35605600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:35603200-35606000	Strong transcription	Fetal Intestine Small	intestine
41	chr14:35603200-35609200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr14:35603200-35623200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr14:35603200-35663400	Weak transcription	Fetal Lung	lung
44	chr14:35603400-35605600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:35603400-35625200	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr14:35603600-35607200	Strong transcription	GM12878-XiMat	blood
47	chr14:35603600-35621600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr14:35604000-35605600	Strong transcription	Hela-S3	cervix
49	chr14:35604000-35606400	Weak transcription	Right Atrium	heart
50	chr14:35604000-35609400	Weak transcription	NHLF	lung

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