Variant report

Variant	nsv564907
Chromosome Location	chr14:65011509-65018663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:611)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:65016898-65017108	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr14:65015764-65016119	IMR90	lung:	n/a	chr14:65015925-65015936
3	CEBPB	chr14:65016989-65017055	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr14:65015867-65016107	HepG2	liver:	n/a	chr14:65015925-65015936
5	CEBPB	chr14:65015808-65016025	H1-hESC	embryonic stem cell:	n/a	chr14:65015925-65015936
6	CEBPB	chr14:65015748-65016753	Hela-S3	cervix:	n/a	chr14:65015925-65015936
7	CEBPB	chr14:65015798-65015979	K562	blood:	n/a	chr14:65015925-65015936
8	CHD2	chr14:65016418-65016760	Hela-S3	cervix:	n/a	chr14:65016637-65016647 chr14:65016625-65016635
9	CTCF	chr14:65016435-65016712	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr14:65016680-65016830	GM12874	blood:	n/a	n/a
11	CTCF	chr14:65016700-65016850	Caco-2	colon:	n/a	n/a
12	CTCF	chr14:65016824-65016860	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr14:65016804-65016844	NHEK	skin:	n/a	n/a
14	CTCF	chr14:65016680-65016830	GM12866	blood:	n/a	n/a
15	CTCF	chr14:65016770-65016855	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:65016751-65016885	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:65016799-65016800	NHEK	skin:	n/a	n/a
18	CTCF	chr14:65016700-65016850	GM12875	blood:	n/a	n/a
19	CTCF	chr14:65016738-65016905	MCF-7	breast:	n/a	n/a
20	E2F1	chr14:65016451-65016831	Hela-S3	cervix:	n/a	n/a
21	E2F6	chr14:65016482-65017304	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr14:65016523-65016748	K562	blood:	n/a	n/a
23	E2F6	chr14:65016431-65016947	H1-hESC	embryonic stem cell:	n/a	n/a
24	ELK1	chr14:65016551-65016763	Hela-S3	cervix:	n/a	n/a
25	ELK4	chr14:65016252-65016764	Hela-S3	cervix:	n/a	n/a
26	FOS	chr14:65015767-65016082	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr14:65015820-65016038	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA3	chr14:65017511-65017710	SH-SY5Y	brain:	n/a	n/a
29	GTF2F1	chr14:65016574-65016616	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr14:65015787-65016676	Hela-S3	cervix:	n/a	n/a
31	HA-E2F1	chr14:65016447-65016870	Hela-S3	cervix:	n/a	n/a
32	HA-E2F1	chr14:65016336-65016984	MCF-7	breast:	n/a	n/a
33	JUND	chr14:65015843-65016032	HepG2	liver:	n/a	n/a
34	JUND	chr14:65011392-65011619	HepG2	liver:	n/a	chr14:65011537-65011545 chr14:65011536-65011545 chr14:65011535-65011546 chr14:65011537-65011544
35	MAFK	chr14:65015949-65016077	HepG2	liver:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
36	MAFK	chr14:65015832-65016078	HepG2	liver:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
37	MAFK	chr14:65015787-65016232	Hela-S3	cervix:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
38	MAFK	chr14:65016509-65016826	Hela-S3	cervix:	n/a	n/a
39	MAX	chr14:65016400-65017057	MCF-7	breast:	n/a	n/a
40	MAX	chr14:65016921-65017121	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr14:65016522-65016824	K562	blood:	n/a	n/a
42	MAX	chr14:65016460-65016902	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr14:65016468-65017093	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr14:65016382-65016914	A549	lung:	n/a	n/a
45	MAX	chr14:65016344-65016854	Hela-S3	cervix:	n/a	n/a
46	MAX	chr14:65016507-65016901	A549	lung:	n/a	n/a
47	MAX	chr14:65016547-65016833	NB4	blood:	n/a	n/a
48	MAZ	chr14:65016516-65016783	Hela-S3	cervix:	n/a	n/a
49	MXI1	chr14:65016419-65016767	Hela-S3	cervix:	n/a	n/a
50	MYC	chr14:65016747-65016857	MCF-7	breast:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65016545-65016595	AG04449	skin:	fetal
2	chr14:65016545-65016595	AG04449	skin:	fetal
3	chr14:65016595-65016645	CMK	blood:	n/a
4	chr14:65016595-65016645	HCF	heart:	n/a
5	chr14:65017091-65017141	HMEC	breast:	n/a
6	chr14:65017091-65017141	SK-N-MC	brain:	n/a
7	chr14:65016591-65016641	AG04450	lung:	fetal
8	chr14:65016802-65016852	ovcar-3	ovarian:	n/a
9	chr14:65012783-65012833	Jurkat	blood:	n/a
10	chr14:65015998-65016048	NHDF-neo	bronchial:	n/a
11	chr14:65017091-65017141	Caco-2	colon:	n/a
12	chr14:65017091-65017141	Hela-S3	cervix:	n/a
13	chr14:65016545-65016595	IMR90	lung:	fetal
14	chr14:65016602-65016652	HEEpiC	esophagus:	n/a
15	chr14:65016517-65016567	SK-N-MC	brain:	n/a
16	chr14:65017091-65017141	T-47D	breast:	n/a
17	chr14:65016802-65016852	T-47D	breast:	n/a
18	chr14:65016802-65016852	HNPCEpiC	eye:	n/a
19	chr14:65016545-65016595	MCF-7	breast:	n/a
20	chr14:65016517-65016567	RPTEC	kidney:	n/a
21	chr14:65016258-65016308	SK-N-SH_RA	brain:	n/a
22	chr14:65016545-65016595	NT2-D1	testis:	n/a
23	chr14:65016802-65016852	HRE	kidney:	n/a
24	chr14:65016595-65016645	HUVEC	blood vessel:	n/a
25	chr14:65016545-65016595	AG09319	gingival:	n/a
26	chr14:65016517-65016567	HMEC	breast:	n/a
27	chr14:65016802-65016852	BE2_C	brain:	n/a
28	chr14:65016517-65016567	SK-N-SH	brain:	n/a
29	chr14:65017091-65017141	GM06990	blood:	n/a
30	chr14:65016602-65016652	SK-N-SH	brain:	n/a
31	chr14:65015998-65016048	NH-A	brain:	n/a
32	chr14:65016602-65016652	SKMC	muscle:	n/a
33	chr14:65012783-65012833	SKMC	muscle:	n/a
34	chr14:65016517-65016567	IMR90	lung:	fetal
35	chr14:65016258-65016308	Caco-2	colon:	n/a
36	chr14:65016602-65016652	H1-hESC	embryonic stem cell:	embryo
37	chr14:65016545-65016595	Jurkat	blood:	n/a
38	chr14:65016802-65016852	MCF10A-Er-Src	breast:	n/a
39	chr14:65016802-65016852	AG09319	gingival:	n/a
40	chr14:65016591-65016641	GM12878	blood:	n/a
41	chr14:65016802-65016852	SK-N-MC	brain:	n/a
42	chr14:65016591-65016641	SK-N-SH_RA	brain:	n/a
43	chr14:65016602-65016652	AG10803	skin:	n/a
44	chr14:65016258-65016308	HUVEC	blood vessel:	n/a
45	chr14:65016591-65016641	MCF10A-Er-Src	breast:	n/a
46	chr14:65016517-65016567	AG10803	skin:	n/a
47	chr14:65017091-65017141	GM12891	blood:	n/a
48	chr14:65017091-65017141	IMR90	lung:	fetal
49	chr14:65016591-65016641	GM19239	blood:	n/a
50	chr14:65012783-65012833	T-47D	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65006961..65009286-chr14:65016299..65018796,2	K562	blood:
2	chr14:64967941..64976890-chr14:65001097..65012463,31	MCF-7	breast:
3	chr14:65005138..65007971-chr14:65016762..65019337,2	MCF-7	breast:
4	chr14:65006007..65010466-chr14:65011368..65016510,6	MCF-7	breast:
5	chr14:65017028..65018763-chr14:65046297..65047824,2	MCF-7	breast:
6	chr14:64971147..64972847-chr14:65015662..65018406,2	MCF-7	breast:
7	chr14:65006111..65008789-chr14:65009033..65011662,5	MCF-7	breast:
8	chr14:65015799..65018122-chr20:55818007..55820214,2	MCF-7	breast:
9	chr14:65005373..65008937-chr14:65014849..65020282,8	MCF-7	breast:
10	chr14:64969437..64972776-chr14:65017251..65021474,5	MCF-7	breast:

No data

Variant related genes	Relation type
PPP1R36	TF binding region
ENSG00000259116	TF binding region
PPP1R36	CpG island
ENSG00000259116	CpG island
ENSG00000126803	chromatin interactions
ENSG00000259116	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000126804	chromatin interactions

Extended variants
information (count: 230 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:230 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2123463	chr14:65011509-65011510	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188334986	chr14:65011523-65011524	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs371909201	chr14:65011536-65011537	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs542146703	chr14:65011564-65011565	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs543095274	chr14:65011595-65011596	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs192264156	chr14:65011614-65011615	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs74894009	chr14:65011615-65011616	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs562970208	chr14:65011626-65011627	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs74056462	chr14:65011627-65011628	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs56357777	chr14:65011629-65011630	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs543759163	chr14:65011664-65011665	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs58644746	chr14:65011672-65011673	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539496232	chr14:65011708-65011709	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs552835649	chr14:65011811-65011812	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs572986469	chr14:65011886-65011887	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs541801078	chr14:65011945-65011946	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs150228153	chr14:65011961-65011962	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs75371963	chr14:65011982-65011983	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs375212955	chr14:65012001-65012002	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs34840868	chr14:65012050-65012051	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs575577348	chr14:65012074-65012075	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs375796597	chr14:65012077-65012078	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs564285386	chr14:65012103-65012104	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs368581222	chr14:65012173-65012174	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs143607264	chr14:65012187-65012188	Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs148921469	chr14:65012226-65012227	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs565581659	chr14:65012239-65012240	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs559380503	chr14:65012242-65012243	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs375021897	chr14:65012263-65012264	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs528566442	chr14:65012272-65012273	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs527975838	chr14:65012291-65012292	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs183731151	chr14:65012318-65012319	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs147036490	chr14:65012349-65012350	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs138168813	chr14:65012364-65012365	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs551016271	chr14:65012367-65012368	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs12889677	chr14:65012449-65012450	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560073242	chr14:65012528-65012529	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs112129406	chr14:65012559-65012560	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs567845419	chr14:65012581-65012582	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539607785	chr14:65012729-65012730	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547222017	chr14:65012749-65012750	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77842555	chr14:65012783-65012784	Enhancers Weak transcription Flanking Active TSS	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs74947527	chr14:65012784-65012785	Enhancers Weak transcription Flanking Active TSS	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs8016361	chr14:65012791-65012792	Enhancers Weak transcription Flanking Active TSS	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs575160695	chr14:65012817-65012818	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs550322064	chr14:65012851-65012852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538140598	chr14:65012981-65012982	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111859135	chr14:65012995-65012996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs577877660	chr14:65013016-65013017	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143769655	chr14:65013053-65013054	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Hematopoietic stem cell	20738155	CNVD
Cancer	17440070	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65005800-65011600	Active TSS	Brain Anterior Caudate	brain
2	chr14:65005800-65012000	Active TSS	Brain Angular Gyrus	brain
3	chr14:65005800-65012000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:65006000-65012000	Active TSS	Brain Substantia Nigra	brain
5	chr14:65006400-65012000	Active TSS	Brain Cingulate Gyrus	brain
6	chr14:65006400-65012400	Active TSS	Brain Hippocampus Middle	brain
7	chr14:65008200-65011800	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr14:65008600-65016200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:65008800-65011600	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr14:65009000-65016200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:65009200-65011600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:65009200-65012200	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr14:65009400-65011600	Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr14:65009400-65012000	Active TSS	H1 Cell Line	embryonic stem cell
15	chr14:65009400-65013000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:65009400-65016600	Weak transcription	Gastric	stomach
17	chr14:65009600-65012000	Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr14:65009600-65016200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr14:65009800-65012200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:65010200-65015600	Weak transcription	Psoas Muscle	Psoas
21	chr14:65010400-65015800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr14:65010400-65015800	Weak transcription	Stomach Smooth Muscle	stomach
23	chr14:65010400-65016600	Weak transcription	Aorta	Aorta
24	chr14:65010600-65012000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr14:65010600-65012000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:65010600-65012000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr14:65010800-65011600	Flanking Active TSS	A549	lung
28	chr14:65010800-65011800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr14:65011000-65011600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr14:65011000-65011600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr14:65011200-65011600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr14:65011200-65011600	Flanking Active TSS	NHLF	lung
33	chr14:65011200-65015800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:65011400-65011600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr14:65011400-65011600	Enhancers	Colon Smooth Muscle	Colon
36	chr14:65011400-65011800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr14:65011400-65011800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr14:65011400-65012600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr14:65011400-65015800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:65011400-65016000	Weak transcription	NHDF-Ad	bronchial
41	chr14:65011600-65011800	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr14:65011600-65011800	Active TSS	A549	lung
43	chr14:65011600-65012200	Weak transcription	Brain Anterior Caudate	brain
44	chr14:65011600-65012400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr14:65011600-65016000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:65011600-65016000	Weak transcription	Colon Smooth Muscle	Colon
47	chr14:65011600-65016000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr14:65011600-65016000	Weak transcription	NHLF	lung
49	chr14:65011600-65016200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr14:65011800-65012000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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