Variant report

Variant	esv32836
Chromosome Location	chr14:78119497-78124958
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	BHLHE40	chr14:78121372-78121649	K562	blood:	n/a	n/a
2	BHLHE40	chr14:78121360-78121629	GM12878	blood:	n/a	n/a
3	BRCA1	chr14:78121264-78121535	HepG2	liver:	n/a	n/a
4	CTCF	chr14:78121363-78121631	Lung_OC	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
5	CTCF	chr14:78119845-78120088	HepG2	liver:	n/a	chr14:78119998-78120011
6	CTCF	chr14:78121420-78121570	AG09309	skin:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
7	CTCF	chr14:78121760-78121910	GM12871	blood:	n/a	n/a
8	CTCF	chr14:78121283-78121710	IMR90	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
9	CTCF	chr14:78119880-78120030	HUVEC	blood vessel:	n/a	chr14:78119998-78120011
10	CTCF	chr14:78121460-78121610	Caco-2	colon:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
11	CTCF	chr14:78119900-78120050	WI-38	lung:	n/a	chr14:78119998-78120011
12	CTCF	chr14:78121420-78121570	AG04450	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
13	CTCF	chr14:78119900-78120050	SAEC	small airway:	n/a	chr14:78119998-78120011
14	CTCF	chr14:78119941-78120086	MCF-7	breast:	n/a	chr14:78119998-78120011
15	CTCF	chr14:78119920-78120070	HCM	heart:	n/a	chr14:78119998-78120011
16	CTCF	chr14:78121420-78121570	GM12878	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
17	CTCF	chr14:78119780-78119930	HRE	kidney:	n/a	n/a
18	CTCF	chr14:78121361-78121613	GM10266	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
19	CTCF	chr14:78121420-78121570	HepG2	liver:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
20	CTCF	chr14:78121368-78121818	MCF-7	breast:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
21	CTCF	chr14:78119943-78120043	GM10266	blood:	n/a	chr14:78119998-78120011
22	CTCF	chr14:78121380-78121661	MCF-7	breast:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
23	CTCF	chr14:78121391-78121693	K562	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
24	CTCF	chr14:78121440-78121590	HepG2	liver:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
25	CTCF	chr14:78120820-78120970	WI-38	lung:	n/a	n/a
26	CTCF	chr14:78121440-78121590	A549	lung:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
27	CTCF	chr14:78121181-78121208	GM19240	blood:	n/a	n/a
28	CTCF	chr14:78120000-78120150	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr14:78121420-78121570	GM12869	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
30	CTCF	chr14:78121400-78121550	HL-60	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
31	CTCF	chr14:78121440-78121590	HCT-116	colon:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
32	CTCF	chr14:78119924-78120085	MCF-7	breast:	n/a	chr14:78119998-78120011
33	CTCF	chr14:78121400-78121550	HVMF	connective:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
34	CTCF	chr14:78119900-78120050	HVMF	connective:	n/a	chr14:78119998-78120011
35	CTCF	chr14:78119960-78120110	NHLF	lung:	n/a	chr14:78119998-78120011
36	CTCF	chr14:78119940-78120090	HCT-116	colon:	n/a	chr14:78119998-78120011
37	CTCF	chr14:78121360-78121510	HMEC	breast:	n/a	n/a
38	CTCF	chr14:78119980-78120130	AG09309	skin:	n/a	chr14:78119998-78120011
39	CTCF	chr14:78121460-78121610	HEK293	kidney:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
40	CTCF	chr14:78119920-78120070	BJ	skin:	n/a	chr14:78119998-78120011
41	CTCF	chr14:78119920-78120070	AG04449	skin:	n/a	chr14:78119998-78120011
42	CTCF	chr14:78120931-78121947	SK-N-SH	brain:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
43	CTCF	chr14:78120080-78120230	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr14:78121440-78121590	GM12873	blood:	n/a	chr14:78121501-78121522 chr14:78121504-78121512 chr14:78121499-78121517
45	CTCF	chr14:78119880-78120030	GM12865	blood:	n/a	chr14:78119998-78120011
46	CTCF	chr14:78121735-78121749	GM19239	blood:	n/a	n/a
47	CTCF	chr14:78119880-78120030	GM12864	blood:	n/a	chr14:78119998-78120011
48	CTCF	chr14:78119920-78120070	Hela-S3	cervix:	n/a	chr14:78119998-78120011
49	CTCF	chr14:78119900-78120050	NHEK	skin:	n/a	chr14:78119998-78120011
50	CTCF	chr14:78119980-78120130	HBMEC	blood vessel:	n/a	chr14:78119998-78120011

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78121495-78121545	HNPCEpiC	eye:	n/a
2	chr14:78121495-78121545	HNPCEpiC	eye:	n/a
3	chr14:78121495-78121545	U87	brain:	n/a
4	chr14:78121495-78121545	HRPEpiC	eye:	n/a
5	chr14:78121495-78121545	MCF-7	breast:	n/a
6	chr14:78121495-78121545	SK-N-SH	brain:	n/a
7	chr14:78121495-78121545	Hepatocyte	liver:	n/a
8	chr14:78121495-78121545	GM12878	blood:	n/a
9	chr14:78121495-78121545	Jurkat	blood:	n/a
10	chr14:78121495-78121545	AoSMC	blood vessel:	n/a
11	chr14:78121495-78121545	NHDF-neo	bronchial:	n/a
12	chr14:78121495-78121545	SAEC	small airway:	n/a
13	chr14:78121495-78121545	ECC-1	luminal epithelium:	n/a
14	chr14:78121495-78121545	A549	lung:	n/a
15	chr14:78121495-78121545	LNCaP	prostate:	n/a
16	chr14:78121495-78121545	HCT-116	colon:	n/a
17	chr14:78121495-78121545	MCF10A-Er-Src	breast:	n/a
18	chr14:78121495-78121545	PFSK-1	brain:	n/a
19	chr14:78121495-78121545	NB4	blood:	n/a
20	chr14:78121495-78121545	NT2-D1	testis:	n/a
21	chr14:78121495-78121545	HAEpiC	amniotic membrane:	n/a
22	chr14:78121495-78121545	SKMC	muscle:	n/a
23	chr14:78121495-78121545	GM19239	blood:	n/a
24	chr14:78121495-78121545	HIPEpiC	eye:	n/a
25	chr14:78121495-78121545	HEK293	kidney:	embryo
26	chr14:78121495-78121545	ovcar-3	ovarian:	n/a
27	chr14:78121495-78121545	GM06990	blood:	n/a
28	chr14:78121495-78121545	HCF	heart:	n/a
29	chr14:78121495-78121545	HEEpiC	esophagus:	n/a
30	chr14:78121495-78121545	HMEC	breast:	n/a
31	chr14:78121495-78121545	AG09309	skin:	n/a
32	chr14:78121495-78121545	PANC-1	pancreas:	n/a
33	chr14:78121495-78121545	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:78121495-78121545	SK-N-SH_RA	brain:	n/a
35	chr14:78121495-78121545	AG04449	skin:	fetal
36	chr14:78121495-78121545	K562	blood:	n/a
37	chr14:78121495-78121545	RPTEC	kidney:	n/a
38	chr14:78121495-78121545	HCM	heart:	n/a
39	chr14:78121495-78121545	BJ	skin:	n/a
40	chr14:78121495-78121545	AG04450	lung:	fetal
41	chr14:78121495-78121545	CMK	blood:	n/a
42	chr14:78121495-78121545	Caco-2	colon:	n/a
43	chr14:78121495-78121545	NH-A	brain:	n/a
44	chr14:78121495-78121545	AG09319	gingival:	n/a
45	chr14:78121495-78121545	IMR90	lung:	fetal
46	chr14:78121495-78121545	PrEC	prostate:	n/a
47	chr14:78121495-78121545	HUVEC	blood vessel:	n/a
48	chr14:78121495-78121545	HRCEpiC	kidney:	n/a
49	chr14:78121495-78121545	HCPEpiC	choroid plexus:	n/a
50	chr14:78121495-78121545	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:78081876..78084095-chr14:78119324..78121053,2	MCF-7	breast:
2	chr14:78116603..78122891-chr14:78172785..78176058,7	MCF-7	breast:
3	chr14:78121033..78121732-chr14:78283460..78284088,3	MCF-7	breast:
4	chr14:78123704..78125775-chr14:78174228..78176042,2	MCF-7	breast:
5	chr14:78121069..78121988-chr14:78173226..78174334,8	MCF-7	breast:
6	chr14:78124444..78126288-chr14:78139672..78142055,2	K562	blood:
7	chr14:78083002..78083811-chr14:78120998..78121918,2	MCF-7	breast:

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

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

Extended variants
information (count: 239 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:239 , 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	rs573440885	chr14:78119500-78119501	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs7150435	chr14:78119534-78119535	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534159620	chr14:78119650-78119651	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547943473	chr14:78119676-78119677	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs570973366	chr14:78119684-78119685	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs373621458	chr14:78119715-78119716	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs371545534	chr14:78119719-78119720	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs539911568	chr14:78119729-78119730	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs185108018	chr14:78119761-78119762	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs556797717	chr14:78119763-78119764	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs116950581	chr14:78119785-78119786	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs558157122	chr14:78119786-78119787	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs535814222	chr14:78119793-78119794	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs145233870	chr14:78119795-78119796	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs57287529	chr14:78119821-78119822	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs61292971	chr14:78119842-78119843	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs397963848	chr14:78119843-78119844	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs571974901	chr14:78119851-78119852	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs2886123	chr14:78119878-78119879	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs113868459	chr14:78119881-78119882	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs577342657	chr14:78119907-78119908	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs148073297	chr14:78119912-78119913	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141790162	chr14:78119932-78119933	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs12886970	chr14:78119950-78119951	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12881530	chr14:78119978-78119979	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs559580496	chr14:78119980-78119981	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs528360290	chr14:78120004-78120005	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs547834233	chr14:78120012-78120013	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs570812371	chr14:78120023-78120024	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs539947276	chr14:78120027-78120028	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs550240332	chr14:78120062-78120063	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs4479155	chr14:78120104-78120105	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189293099	chr14:78120146-78120147	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs541508032	chr14:78120169-78120170	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs7145210	chr14:78120184-78120185	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572424487	chr14:78120238-78120239	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs17752274	chr14:78120249-78120250	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs7144314	chr14:78120251-78120252	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs557336408	chr14:78120277-78120278	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs577179438	chr14:78120307-78120308	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs550585828	chr14:78120371-78120372	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs181634845	chr14:78120410-78120411	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs560966077	chr14:78120433-78120434	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs184414385	chr14:78120453-78120454	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs138599251	chr14:78120492-78120493	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs7144524	chr14:78120523-78120524	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528397118	chr14:78120532-78120533	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs189890417	chr14:78120550-78120551	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs571468617	chr14:78120560-78120561	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs564511924	chr14:78120561-78120562	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 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:161 , 50 per page) page: 1 2 3 4

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

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