Variant report

Variant	nsv976349
Chromosome Location	chr14:68171328-68181608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:68171192-68171429	K562	blood:	n/a	n/a
2	BHLHE40	chr14:68171303-68171647	K562	blood:	n/a	n/a
3	CBX3	chr14:68174702-68174949	K562	blood:	n/a	n/a
4	CBX3	chr14:68176987-68177344	HCT-116	colon:	n/a	n/a
5	CBX3	chr14:68177056-68177272	K562	blood:	n/a	n/a
6	CBX3	chr14:68176929-68177374	HCT-116	colon:	n/a	n/a
7	CBX3	chr14:68174636-68174984	K562	blood:	n/a	n/a
8	CEBPB	chr14:68176114-68176358	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:68176148-68176288	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr14:68171271-68171481	GM10248	blood:	n/a	n/a
11	CTCF	chr14:68171260-68171410	NHLF	lung:	n/a	n/a
12	CTCF	chr14:68171217-68171527	Medullo	brain:	n/a	n/a
13	CTCF	chr14:68171300-68171450	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr14:68171320-68171470	AG04449	skin:	n/a	n/a
15	CTCF	chr14:68171320-68171470	Caco-2	colon:	n/a	n/a
16	CTCF	chr14:68171320-68171470	HFF	foreskin:	n/a	n/a
17	CTCF	chr14:68171300-68171450	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr14:68171643-68171729	GM19238	blood:	n/a	n/a
19	CTCF	chr14:68171300-68171450	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr14:68171206-68171554	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr14:68171190-68171459	ECC-1	luminal epithelium:	n/a	n/a
22	CTCF	chr14:68171270-68171451	GM19239	blood:	n/a	n/a
23	CTCF	chr14:68171280-68171430	HMEC	breast:	n/a	n/a
24	CTCF	chr14:68171280-68171430	HL-60	blood:	n/a	n/a
25	CTCF	chr14:68171260-68171410	WI-38	lung:	n/a	n/a
26	CTCF	chr14:68171206-68171450	K562	blood:	n/a	n/a
27	CTCF	chr14:68171300-68171450	HMF	breast:	n/a	n/a
28	CTCF	chr14:68171300-68171450	HPF	lung:	n/a	n/a
29	CTCF	chr14:68171300-68171450	GM12875	blood:	n/a	n/a
30	CTCF	chr14:68171300-68171450	HMEC	breast:	n/a	n/a
31	CTCF	chr14:68171260-68171410	GM12866	blood:	n/a	n/a
32	CTCF	chr14:68171274-68171491	LNCaP	prostate:	n/a	n/a
33	CTCF	chr14:68171280-68171430	HEK293	kidney:	n/a	n/a
34	CTCF	chr14:68171280-68171430	GM12868	blood:	n/a	n/a
35	CTCF	chr14:68171320-68171470	GM12801	blood:	n/a	n/a
36	CTCF	chr14:68171166-68171540	T-47D	breast:	n/a	n/a
37	CTCF	chr14:68171260-68171410	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr14:68171300-68171450	NHEK	skin:	n/a	n/a
39	CTCF	chr14:68171340-68171490	HCM	heart:	n/a	n/a
40	CTCF	chr14:68171224-68171516	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:68171320-68171470	GM12866	blood:	n/a	n/a
42	CTCF	chr14:68171261-68171494	HepG2	liver:	n/a	n/a
43	CTCF	chr14:68171178-68171529	A549	lung:	n/a	n/a
44	CTCF	chr14:68171340-68171490	GM12864	blood:	n/a	n/a
45	CTCF	chr14:68171225-68171507	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr14:68171300-68171450	BJ	skin:	n/a	n/a
47	CTCF	chr14:68171320-68171470	NHEK	skin:	n/a	n/a
48	CTCF	chr14:68171300-68171450	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr14:68171280-68171430	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr14:68171280-68171430	GM12867	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:68171536-68171586	AG04449	skin:	fetal
2	chr14:68171536-68171586	BE2_C	brain:	n/a
3	chr14:68171536-68171586	H1-hESC	embryonic stem cell:	embryo
4	chr14:68171536-68171586	GM12891	blood:	n/a
5	chr14:68171536-68171586	GM19239	blood:	n/a
6	chr14:68171536-68171586	SK-N-MC	brain:	n/a
7	chr14:68171536-68171586	HRPEpiC	eye:	n/a
8	chr14:68171536-68171586	HCM	heart:	n/a
9	chr14:68171536-68171586	HL-60	blood:	n/a
10	chr14:68171536-68171586	HAEpiC	amniotic membrane:	n/a
11	chr14:68171536-68171586	LNCaP	prostate:	n/a
12	chr14:68171536-68171586	NB4	blood:	n/a
13	chr14:68171536-68171586	GM12892	blood:	n/a
14	chr14:68171536-68171586	Hela-S3	cervix:	n/a
15	chr14:68171536-68171586	NT2-D1	testis:	n/a
16	chr14:68171536-68171586	HEEpiC	esophagus:	n/a
17	chr14:68171536-68171586	HCPEpiC	choroid plexus:	n/a
18	chr14:68171536-68171586	NHBE	bronchial:	n/a
19	chr14:68171536-68171586	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:68171536-68171586	HRCEpiC	kidney:	n/a
21	chr14:68171536-68171586	AG04450	lung:	fetal
22	chr14:68171536-68171586	HRE	kidney:	n/a
23	chr14:68171536-68171586	HCF	heart:	n/a
24	chr14:68171536-68171586	IMR90	lung:	fetal
25	chr14:68171536-68171586	SAEC	small airway:	n/a
26	chr14:68171536-68171586	MCF10A-Er-Src	breast:	n/a
27	chr14:68171536-68171586	NHDF-neo	bronchial:	n/a
28	chr14:68171536-68171586	PFSK-1	brain:	n/a
29	chr14:68171536-68171586	MCF-7	breast:	n/a
30	chr14:68171536-68171586	PrEC	prostate:	n/a
31	chr14:68171536-68171586	ovcar-3	ovarian:	n/a
32	chr14:68171536-68171586	HEK293	kidney:	embryo
33	chr14:68171536-68171586	AG10803	skin:	n/a
34	chr14:68171536-68171586	HepG2	liver:	n/a
35	chr14:68171536-68171586	ProgFib	skin:	n/a
36	chr14:68171536-68171586	HNPCEpiC	eye:	n/a
37	chr14:68171536-68171586	PANC-1	pancreas:	n/a
38	chr14:68171536-68171586	RPTEC	kidney:	n/a
39	chr14:68171536-68171586	AG09309	skin:	n/a
40	chr14:68171536-68171586	T-47D	breast:	n/a
41	chr14:68171536-68171586	GM06990	blood:	n/a
42	chr14:68171536-68171586	Hepatocyte	liver:	n/a
43	chr14:68171536-68171586	Jurkat	blood:	n/a
44	chr14:68171536-68171586	HUVEC	blood vessel:	n/a
45	chr14:68171536-68171586	K562	blood:	n/a
46	chr14:68171536-68171586	HMEC	breast:	n/a
47	chr14:68171536-68171586	AoSMC	blood vessel:	n/a
48	chr14:68171536-68171586	CMK	blood:	n/a
49	chr14:68171536-68171586	AG09319	gingival:	n/a
50	chr14:68171536-68171586	NH-A	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:68133599..68134168-chr14:68170909..68171445,2	MCF-7	breast:
2	chr14:68083632..68084176-chr14:68170942..68171834,2	K562	blood:
3	chr14:68050285..68051265-chr14:68171010..68171830,2	MCF-7	breast:
4	chr14:68139698..68142484-chr14:68169874..68172946,4	MCF-7	breast:
5	chr14:68085030..68085991-chr14:68170815..68171645,4	MCF-7	breast:
6	chr14:67090731..67091375-chr14:68170944..68171444,2	MCF-7	breast:
7	chr14:68181604..68183336-chr14:68184866..68187768,3	K562	blood:
8	chr14:68161792..68164356-chr14:68169236..68171815,2	MCF-7	breast:
9	chr14:68085038..68085996-chr14:68170872..68171824,5	K562	blood:
10	chr14:67993411..67993949-chr14:68170946..68171642,2	MCF-7	breast:
11	chr14:68049889..68051990-chr14:68169863..68172640,4	MCF-7	breast:
12	chr14:68065457..68068095-chr14:68169119..68171833,2	MCF-7	breast:
13	chr14:68050450..68051460-chr14:68170491..68171891,10	K562	blood:
14	chr14:68171220..68171774-chr14:68232579..68233209,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARG2-8	chr14:68181262-68181422	NONHSAT037467
2	lnc-ARG2-7	chr14:68172671-68172972	NONHSAT037466

No data

Variant related genes	Relation type
RPL21P9	TF binding region
RDH12	TF binding region
RN7SL369P	TF binding region
RPL21P9	CpG island
RDH12	CpG island
RN7SL369P	CpG island
ENSG00000201529	chromatin interactions
ENSG00000054690	chromatin interactions
ENSG00000139988	chromatin interactions
ENSG00000072042	chromatin interactions
ENSG00000100564	chromatin interactions
ENSG00000100568	chromatin interactions

Extended variants
information (count: 347 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:347 , 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	rs12147616	chr14:68171340-68171341	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143446862	chr14:68171382-68171383	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs76336046	chr14:68171432-68171433	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs535979681	chr14:68171505-68171506	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs141584046	chr14:68171541-68171542	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs572427724	chr14:68171600-68171601	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs184712192	chr14:68171629-68171630	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs117569446	chr14:68171633-68171634	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs368378559	chr14:68171656-68171657	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs551205310	chr14:68171675-68171676	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs569737652	chr14:68171695-68171696	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs544022113	chr14:68171696-68171697	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs12882315	chr14:68171728-68171729	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs574425217	chr14:68171834-68171835	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs541929113	chr14:68171839-68171840	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs112998406	chr14:68171868-68171869	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs12435352	chr14:68171890-68171891	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34074397	chr14:68171928-68171929	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs112313306	chr14:68172029-68172030	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564039211	chr14:68172098-68172099	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs76820548	chr14:68172107-68172108	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369047471	chr14:68172219-68172220	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs143974932	chr14:68172247-68172248	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568274893	chr14:68172255-68172256	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs535019119	chr14:68172328-68172329	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs535550634	chr14:68172358-68172359	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs547878151	chr14:68172433-68172434	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566031927	chr14:68172472-68172473	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539838774	chr14:68172479-68172480	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558223591	chr14:68172487-68172488	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs530345066	chr14:68172634-68172635	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187561129	chr14:68172669-68172670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs555650347	chr14:68172677-68172678	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs574190367	chr14:68172697-68172698	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs147282774	chr14:68172714-68172715	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs373413139	chr14:68172746-68172747	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs553837386	chr14:68172778-68172779	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs571858961	chr14:68172794-68172795	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs56024347	chr14:68172800-68172801	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs535679765	chr14:68172832-68172833	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs563773185	chr14:68172879-68172880	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs1117516	chr14:68172894-68172895	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140817332	chr14:68172914-68172915	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs368884790	chr14:68172959-68172960	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs73276639	chr14:68172963-68172964	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557558098	chr14:68172968-68172969	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs149786584	chr14:68172996-68172997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192165425	chr14:68173185-68173186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533497551	chr14:68173202-68173203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551777796	chr14:68173204-68173205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68162600-68171400	Weak transcription	Aorta	Aorta
2	chr14:68162600-68171600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:68168800-68171400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:68170400-68171400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr14:68170400-68172000	Enhancers	Liver	Liver
6	chr14:68171000-68171400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr14:68171000-68171400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:68171000-68171800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:68171000-68172000	Enhancers	Stomach Mucosa	stomach
10	chr14:68171000-68172400	Enhancers	A549	lung
11	chr14:68171200-68171400	Flanking Active TSS	Brain Angular Gyrus	brain
12	chr14:68171200-68171600	Enhancers	Duodenum Mucosa	Duodenum
13	chr14:68171200-68171800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr14:68171200-68171800	Enhancers	HepG2	liver
15	chr14:68171200-68171800	Enhancers	K562	blood
16	chr14:68171200-68172000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:68171200-68172000	Flanking Active TSS	Brain Substantia Nigra	brain
18	chr14:68171200-68172200	Enhancers	Brain Hippocampus Middle	brain
19	chr14:68171200-68172200	Enhancers	HMEC	breast
20	chr14:68171200-68172400	Enhancers	Brain Anterior Caudate	brain
21	chr14:68171200-68172400	Enhancers	Hela-S3	cervix
22	chr14:68171400-68171600	Enhancers	Aorta	Aorta
23	chr14:68171400-68171600	Active TSS	Brain Angular Gyrus	brain
24	chr14:68171400-68171600	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr14:68171400-68171600	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr14:68171400-68171800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:68171400-68171800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr14:68171400-68172200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:68171400-68172200	Enhancers	NHEK	skin
30	chr14:68171600-68171800	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr14:68171600-68171800	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr14:68171600-68171800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:68171600-68171800	Enhancers	Rectal Smooth Muscle	rectum
34	chr14:68171600-68172200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:68171600-68172200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:68171600-68172200	Enhancers	Brain Cingulate Gyrus	brain
37	chr14:68171800-68172000	Enhancers	Brain Angular Gyrus	brain
38	chr14:68171800-68181600	Weak transcription	K562	blood
39	chr14:68172000-68172200	Enhancers	Brain Substantia Nigra	brain
40	chr14:68172000-68175600	Weak transcription	Liver	Liver
41	chr14:68172400-68176000	Weak transcription	Hela-S3	cervix
42	chr14:68175600-68177000	Enhancers	Liver	Liver
43	chr14:68176000-68176400	Enhancers	Hela-S3	cervix
44	chr14:68176200-68177000	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr14:68176400-68176600	Flanking Active TSS	Hela-S3	cervix
46	chr14:68176400-68177000	Enhancers	Fetal Intestine Large	intestine
47	chr14:68176600-68176800	Enhancers	Hela-S3	cervix
48	chr14:68176800-68177000	Flanking Active TSS	Hela-S3	cervix
49	chr14:68177000-68177400	Weak transcription	Fetal Intestine Small	intestine
50	chr14:68177000-68177400	Enhancers	Hela-S3	cervix

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