Variant report

Variant	nsv9155
Chromosome Location	chr14:78118162-78133830
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	BACH1	chr14:78126520-78126677	K562	blood:	n/a	n/a
2	BHLHE40	chr14:78121372-78121649	K562	blood:	n/a	n/a
3	BHLHE40	chr14:78121360-78121629	GM12878	blood:	n/a	n/a
4	BRCA1	chr14:78121264-78121535	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:78126135-78126558	IMR90	lung:	n/a	chr14:78126264-78126275
6	CEBPB	chr14:78129894-78130081	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:78126152-78126438	K562	blood:	n/a	chr14:78126264-78126275
8	CEBPB	chr14:78129812-78130132	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:78126148-78126484	A549	lung:	n/a	chr14:78126264-78126275
10	CEBPB	chr14:78126126-78126512	HepG2	liver:	n/a	chr14:78126264-78126275
11	CEBPB	chr14:78129732-78130172	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:78126192-78126435	Hela-S3	cervix:	n/a	chr14:78126264-78126275
13	CEBPD	chr14:78131600-78131840	K562	blood:	n/a	n/a
14	CTCF	chr14:78121420-78121570	MCF-7	breast:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
15	CTCF	chr14:78119943-78120043	GM10266	blood:	n/a	chr14:78119998-78120011
16	CTCF	chr14:78121400-78121550	HRPEpiC	eye:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
17	CTCF	chr14:78121197-78121808	A549	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
18	CTCF	chr14:78119900-78120050	BJ	skin:	n/a	chr14:78119998-78120011
19	CTCF	chr14:78121440-78121590	HFF	foreskin:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
20	CTCF	chr14:78121420-78121570	AoAF	blood vessel:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
21	CTCF	chr14:78119920-78120070	Caco-2	colon:	n/a	chr14:78119998-78120011
22	CTCF	chr14:78121460-78121610	GM12872	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
23	CTCF	chr14:78121440-78121590	GM12868	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
24	CTCF	chr14:78119940-78120090	HCFaa	heart:	n/a	chr14:78119998-78120011
25	CTCF	chr14:78119920-78120070	HEEpiC	esophagus:	n/a	chr14:78119998-78120011
26	CTCF	chr14:78121440-78121590	RPTEC	kidney:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
27	CTCF	chr14:78119900-78120050	HCPEpiC	choroid plexus:	n/a	chr14:78119998-78120011
28	CTCF	chr14:78121363-78121676	A549	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
29	CTCF	chr14:78119836-78120099	HepG2	liver:	n/a	chr14:78119998-78120011
30	CTCF	chr14:78119900-78120050	BE2_C	brain:	n/a	chr14:78119998-78120011
31	CTCF	chr14:78121460-78121610	HVMF	connective:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
32	CTCF	chr14:78121420-78121570	AG09309	skin:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
33	CTCF	chr14:78121460-78121610	NHEK	skin:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
34	CTCF	chr14:78119900-78120050	GM12873	blood:	n/a	chr14:78119998-78120011
35	CTCF	chr14:78121420-78121570	SAEC	small airway:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
36	CTCF	chr14:78121368-78121666	LNCaP	prostate:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
37	CTCF	chr14:78121420-78121570	HEEpiC	esophagus:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
38	CTCF	chr14:78121391-78121693	K562	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
39	CTCF	chr14:78121340-78121490	A549	lung:	n/a	n/a
40	CTCF	chr14:78121420-78121570	HMF	breast:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
41	CTCF	chr14:78119924-78120085	MCF-7	breast:	n/a	chr14:78119998-78120011
42	CTCF	chr14:78121460-78121610	HFF-Myc	foreskin:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
43	CTCF	chr14:78121373-78121661	A549	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
44	CTCF	chr14:78119954-78120048	GM12892	blood:	n/a	chr14:78119998-78120011
45	CTCF	chr14:78119940-78120090	HCT-116	colon:	n/a	chr14:78119998-78120011
46	CTCF	chr14:78119940-78120090	K562	blood:	n/a	chr14:78119998-78120011
47	CTCF	chr14:78119704-78120226	K562	blood:	n/a	chr14:78119998-78120011
48	CTCF	chr14:78120240-78120390	BE2_C	brain:	n/a	n/a
49	CTCF	chr14:78119835-78120118	IMR90	lung:	n/a	chr14:78119998-78120011
50	CTCF	chr14:78121371-78121634	HepG2	liver:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78128179-78128229	GM12892	blood:	n/a
2	chr14:78128179-78128229	SK-N-SH	brain:	n/a
3	chr14:78121495-78121545	HMEC	breast:	n/a
4	chr14:78128179-78128229	HRCEpiC	kidney:	n/a
5	chr14:78128179-78128229	A549	lung:	n/a
6	chr14:78121495-78121545	SAEC	small airway:	n/a
7	chr14:78121495-78121545	Hela-S3	cervix:	n/a
8	chr14:78121495-78121545	PANC-1	pancreas:	n/a
9	chr14:78128179-78128229	NHBE	bronchial:	n/a
10	chr14:78121495-78121545	GM12878	blood:	n/a
11	chr14:78128179-78128229	ProgFib	skin:	n/a
12	chr14:78121495-78121545	HEK293	kidney:	embryo
13	chr14:78128179-78128229	ECC-1	luminal epithelium:	n/a
14	chr14:78128179-78128229	SK-N-SH_RA	brain:	n/a
15	chr14:78121495-78121545	GM19239	blood:	n/a
16	chr14:78121495-78121545	ECC-1	luminal epithelium:	n/a
17	chr14:78121495-78121545	SKMC	muscle:	n/a
18	chr14:78121495-78121545	LNCaP	prostate:	n/a
19	chr14:78121495-78121545	CMK	blood:	n/a
20	chr14:78128179-78128229	LNCaP	prostate:	n/a
21	chr14:78121495-78121545	H1-hESC	embryonic stem cell:	embryo
22	chr14:78121495-78121545	HRPEpiC	eye:	n/a
23	chr14:78128179-78128229	AG10803	skin:	n/a
24	chr14:78121495-78121545	Hepatocyte	liver:	n/a
25	chr14:78121495-78121545	Caco-2	colon:	n/a
26	chr14:78128179-78128229	HNPCEpiC	eye:	n/a
27	chr14:78128179-78128229	HEK293	kidney:	embryo
28	chr14:78121495-78121545	MCF-7	breast:	n/a
29	chr14:78121495-78121545	SK-N-SH_RA	brain:	n/a
30	chr14:78121495-78121545	NB4	blood:	n/a
31	chr14:78128179-78128229	RPTEC	kidney:	n/a
32	chr14:78128179-78128229	Caco-2	colon:	n/a
33	chr14:78121495-78121545	ovcar-3	ovarian:	n/a
34	chr14:78128179-78128229	K562	blood:	n/a
35	chr14:78121495-78121545	HL-60	blood:	n/a
36	chr14:78128179-78128229	HCF	heart:	n/a
37	chr14:78121495-78121545	HCF	heart:	n/a
38	chr14:78128179-78128229	AG04449	skin:	fetal
39	chr14:78128179-78128229	GM19239	blood:	n/a
40	chr14:78121495-78121545	IMR90	lung:	fetal
41	chr14:78128179-78128229	PANC-1	pancreas:	n/a
42	chr14:78128179-78128229	IMR90	lung:	fetal
43	chr14:78121495-78121545	HCPEpiC	choroid plexus:	n/a
44	chr14:78128179-78128229	SK-N-MC	brain:	n/a
45	chr14:78128179-78128229	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:78121495-78121545	NH-A	brain:	n/a
47	chr14:78128179-78128229	HIPEpiC	eye:	n/a
48	chr14:78128179-78128229	AoSMC	blood vessel:	n/a
49	chr14:78121495-78121545	HEEpiC	esophagus:	n/a
50	chr14:78128179-78128229	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:78121033..78121732-chr14:78283460..78284088,3	MCF-7	breast:
2	chr14:78128574..78130138-chr14:78174155..78175845,2	MCF-7	breast:
3	chr14:78116603..78122891-chr14:78172785..78176058,7	MCF-7	breast:
4	chr14:78123704..78125775-chr14:78174228..78176042,2	MCF-7	breast:
5	chr11:63997554..63998377-chr14:78125701..78126201,2	MCF-7	breast:
6	chr14:78081876..78084095-chr14:78119324..78121053,2	MCF-7	breast:
7	chr14:78132831..78134732-chr14:78142365..78145336,2	MCF-7	breast:
8	chr14:78129873..78132369-chr14:78135143..78137756,2	MCF-7	breast:
9	chr14:78126065..78127777-chr14:78174399..78177097,2	K562	blood:
10	chr14:78133661..78136302-chr14:78138970..78141654,2	K562	blood:
11	chr14:78121069..78121988-chr14:78173226..78174334,8	MCF-7	breast:
12	chr14:78083002..78083811-chr14:78120998..78121918,2	MCF-7	breast:
13	chr14:78126563..78128785-chr14:78225454..78227609,2	K562	blood:
14	chr14:78125349..78126859-chr14:78170133..78172097,2	K562	blood:
15	chr14:78124444..78126288-chr14:78139672..78142055,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALKBH1-2	chr14:78119170-78119398	NONHSAT037995
2	lnc-ALKBH1-1	chr14:78123810-78123921	XLOC_011082
3	lnc-ALKBH1-1	chr14:78123809-78123921	NONHSAT037996
4	lnc-ALKBH1-1	chr14:78122343-78122594	XLOC_011082
5	lnc-ALKBH1-1	chr14:78122342-78122594	NONHSAT037996

Variant related genes	Relation type
COX6CP11	TF binding region
COX6CP11	CpG island
ENSG00000110011	chromatin interactions
ENSG00000100603	chromatin interactions
ENSG00000100601	chromatin interactions
ENSG00000197734	chromatin interactions
ENSG00000100596	chromatin interactions
ENSG00000119705	chromatin interactions

Extended variants
information (count: 648 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17825229	chr14:78118174-78118175	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562508123	chr14:78118216-78118217	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs61236691	chr14:78118217-78118218	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372684594	chr14:78118218-78118219	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531204991	chr14:78118226-78118227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs397829119	chr14:78118233-78118234	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548290377	chr14:78118287-78118288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12881619	chr14:78118334-78118335	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182741885	chr14:78118377-78118378	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76023729	chr14:78118419-78118420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570267680	chr14:78118450-78118451	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139982428	chr14:78118474-78118475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs77320936	chr14:78118509-78118510	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
14	rs568959828	chr14:78118529-78118530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs537830417	chr14:78118536-78118537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs187074035	chr14:78118549-78118550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567446261	chr14:78118552-78118553	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs574853344	chr14:78118555-78118556	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201508695	chr14:78118562-78118563	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs192857804	chr14:78118563-78118564	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373803076	chr14:78118573-78118574	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201421277	chr14:78118574-78118575	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373124082	chr14:78118576-78118577	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs577503911	chr14:78118579-78118580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs199969316	chr14:78118586-78118587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs547819866	chr14:78118587-78118588	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563152858	chr14:78118616-78118617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73305429	chr14:78118678-78118679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541474756	chr14:78118687-78118688	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184665185	chr14:78118696-78118697	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs527396042	chr14:78118703-78118704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs139826903	chr14:78118710-78118711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533152957	chr14:78118717-78118718	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs547050655	chr14:78118738-78118739	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570357009	chr14:78118753-78118754	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532960986	chr14:78118801-78118802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs527603494	chr14:78118809-78118810	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs59451206	chr14:78118895-78118896	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12881757	chr14:78118912-78118913	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs201236443	chr14:78118936-78118937	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535707337	chr14:78118965-78118966	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554689707	chr14:78118969-78118970	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75832085	chr14:78118971-78118972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
44	rs534072257	chr14:78118997-78118998	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554303743	chr14:78119011-78119012	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs144696868	chr14:78119029-78119030	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs79777106	chr14:78119037-78119038	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373793035	chr14:78119046-78119047	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs146688666	chr14:78119126-78119127	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76040962	chr14:78119146-78119147	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78114600-78118600	Weak transcription	HepG2	liver
2	chr14:78115400-78120000	Weak transcription	Fetal Intestine Large	intestine
3	chr14:78115600-78120000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr14:78115600-78120800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr14:78116000-78119800	Weak transcription	Adipose Nuclei	Adipose
6	chr14:78118400-78118800	Enhancers	GM12878-XiMat	blood
7	chr14:78118400-78120200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:78118600-78119800	Enhancers	HepG2	liver
9	chr14:78119600-78120200	Enhancers	K562	blood
10	chr14:78119600-78122000	Enhancers	Pancreas	Pancrea
11	chr14:78119600-78123200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr14:78119800-78120200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:78119800-78120200	Flanking Active TSS	HepG2	liver
14	chr14:78119800-78120800	Enhancers	Placenta	Placenta
15	chr14:78119800-78121200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:78119800-78121400	Enhancers	Primary hematopoietic stem cells	blood
17	chr14:78119800-78121400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr14:78119800-78121400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:78119800-78121800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:78119800-78122000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:78119800-78122000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr14:78119800-78125400	Enhancers	Adipose Nuclei	Adipose
23	chr14:78120000-78120200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:78120000-78120200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:78120000-78120200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr14:78120000-78120200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:78120000-78120400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr14:78120000-78120400	Enhancers	Primary T cells from cord blood	blood
29	chr14:78120000-78120400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:78120000-78120800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr14:78120000-78121400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr14:78120000-78121800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr14:78120000-78121800	Enhancers	Primary B cells from cord blood	blood
34	chr14:78120000-78121800	Enhancers	Duodenum Mucosa	Duodenum
35	chr14:78120000-78122000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr14:78120000-78122000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:78120000-78122000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:78120000-78122000	Enhancers	Fetal Intestine Large	intestine
39	chr14:78120000-78122200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr14:78120200-78120400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr14:78120200-78120400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr14:78120200-78120400	Enhancers	Fetal Brain Female	brain
43	chr14:78120200-78120600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:78120200-78120600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr14:78120200-78120600	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr14:78120200-78120600	Enhancers	Fetal Thymus	thymus
47	chr14:78120200-78120600	Active TSS	HepG2	liver
48	chr14:78120200-78120800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:78120200-78120800	Enhancers	Fetal Muscle Leg	muscle
50	chr14:78120200-78120800	Weak transcription	K562	blood

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