Variant report

Variant	esv3324620
Chromosome Location	chr14:105614932-105617780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:428)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:105617724-105617869	MCF-7	breast:	n/a	n/a
2	CTCF	chr14:105617774-105617835	GM19238	blood:	n/a	n/a
3	CTCF	chr14:105617733-105617877	MCF-7	breast:	n/a	n/a
4	CTCF	chr14:105617757-105617860	GM19239	blood:	n/a	n/a
5	CTCF	chr14:105617724-105617853	GM12892	blood:	n/a	n/a
6	CTCF	chr14:105617724-105617837	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr14:105617731-105617866	Gliobla	brain:	n/a	n/a
8	CTCF	chr14:105617725-105617883	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr14:105617700-105617850	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr14:105617724-105617863	NHEK	skin:	n/a	n/a
11	CTCF	chr14:105617750-105617882	MCF-7	breast:	n/a	n/a
12	CTCF	chr14:105617724-105617855	GM12891	blood:	n/a	n/a
13	EGR1	chr14:105615946-105616154	K562	blood:	n/a	chr14:105616112-105616125
14	ESR1	chr14:105616589-105617029	ECC-1	luminal epithelium:	n/a	chr14:105616912-105616929
15	ESR1	chr14:105616710-105617013	ECC-1	luminal epithelium:	n/a	chr14:105616912-105616929
16	POLR2A	chr14:105615131-105615157	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr14:105615786-105615926	HUVEC	blood vessel:	n/a	n/a
18	ZBTB7A	chr14:105615738-105616105	ECC-1	luminal epithelium:	n/a	n/a
19	ZBTB7A	chr14:105616403-105616831	ECC-1	luminal epithelium:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105615401-105615451	ProgFib	skin:	n/a
2	chr14:105615401-105615451	ProgFib	skin:	n/a
3	chr14:105615401-105615451	GM12878	blood:	n/a
4	chr14:105617080-105617130	AG09319	gingival:	n/a
5	chr14:105616988-105617038	AoSMC	blood vessel:	n/a
6	chr14:105615401-105615451	HepG2	liver:	n/a
7	chr14:105617575-105617625	RPTEC	kidney:	n/a
8	chr14:105617080-105617130	PANC-1	pancreas:	n/a
9	chr14:105617080-105617130	Hepatocyte	liver:	n/a
10	chr14:105617080-105617130	H1-hESC	embryonic stem cell:	embryo
11	chr14:105616988-105617038	Hela-S3	cervix:	n/a
12	chr14:105617080-105617130	HAEpiC	amniotic membrane:	n/a
13	chr14:105617575-105617625	LNCaP	prostate:	n/a
14	chr14:105617575-105617625	ProgFib	skin:	n/a
15	chr14:105617575-105617625	A549	lung:	n/a
16	chr14:105617575-105617625	GM06990	blood:	n/a
17	chr14:105617080-105617130	A549	lung:	n/a
18	chr14:105616988-105617038	AG09319	gingival:	n/a
19	chr14:105615401-105615451	GM12892	blood:	n/a
20	chr14:105615459-105615509	AG10803	skin:	n/a
21	chr14:105617308-105617358	HEEpiC	esophagus:	n/a
22	chr14:105615459-105615509	A549	lung:	n/a
23	chr14:105616988-105617038	HUVEC	blood vessel:	n/a
24	chr14:105617575-105617625	AG10803	skin:	n/a
25	chr14:105617080-105617130	HEK293	kidney:	embryo
26	chr14:105617080-105617130	HIPEpiC	eye:	n/a
27	chr14:105617080-105617130	HepG2	liver:	n/a
28	chr14:105617308-105617358	Caco-2	colon:	n/a
29	chr14:105617308-105617358	HCM	heart:	n/a
30	chr14:105617308-105617358	U87	brain:	n/a
31	chr14:105617575-105617625	T-47D	breast:	n/a
32	chr14:105617575-105617625	NHBE	bronchial:	n/a
33	chr14:105617080-105617130	AG04449	skin:	fetal
34	chr14:105615459-105615509	NB4	blood:	n/a
35	chr14:105617173-105617223	SK-N-SH	brain:	n/a
36	chr14:105616988-105617038	HCF	heart:	n/a
37	chr14:105615401-105615451	HCF	heart:	n/a
38	chr14:105615459-105615509	HRPEpiC	eye:	n/a
39	chr14:105617173-105617223	PFSK-1	brain:	n/a
40	chr14:105615401-105615451	Hepatocyte	liver:	n/a
41	chr14:105617080-105617130	AG09309	skin:	n/a
42	chr14:105617575-105617625	CMK	blood:	n/a
43	chr14:105617173-105617223	AG09319	gingival:	n/a
44	chr14:105617173-105617223	GM06990	blood:	n/a
45	chr14:105615401-105615451	U87	brain:	n/a
46	chr14:105617080-105617130	HNPCEpiC	eye:	n/a
47	chr14:105615401-105615451	NT2-D1	testis:	n/a
48	chr14:105616988-105617038	HCT-116	colon:	n/a
49	chr14:105615401-105615451	H1-hESC	embryonic stem cell:	embryo
50	chr14:105615401-105615451	AG04450	lung:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
2	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
3	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
4	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
5	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
6	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
7	chr14:105438558..105440399-chr14:105616229..105618880,2	MCF-7	breast:
8	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431

No data

Variant related genes	Relation type
JAG2	TF binding region
JAG2	CpG island
ENSG00000184916	chromatin interactions
ENSG00000183828	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2242635	chr14:105614974-105614975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374858897	chr14:105615008-105615009	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587649970	chr14:105615014-105615015	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75980785	chr14:105615021-105615022	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2242634	chr14:105615026-105615027	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs188931696	chr14:105615071-105615072	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs370664484	chr14:105615089-105615090	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs587721157	chr14:105615110-105615111	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149164867	chr14:105615133-105615134	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs375091434	chr14:105615140-105615141	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587757658	chr14:105615152-105615153	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201209535	chr14:105615205-105615206	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200423307	chr14:105615206-105615207	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs374705973	chr14:105615209-105615210	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201802549	chr14:105615210-105615211	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368881790	chr14:105615217-105615218	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs587644459	chr14:105615228-105615229	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372133737	chr14:105615237-105615238	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587624930	chr14:105615238-105615239	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs200017039	chr14:105615254-105615255	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373732223	chr14:105615255-105615256	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201049510	chr14:105615257-105615258	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371745064	chr14:105615262-105615263	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587760128	chr14:105615290-105615291	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376127608	chr14:105615344-105615345	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145041298	chr14:105615359-105615360	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138823032	chr14:105615368-105615369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201468009	chr14:105615370-105615371	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369686885	chr14:105615381-105615382	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs141987287	chr14:105615389-105615390	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs145627661	chr14:105615397-105615398	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs138503062	chr14:105615402-105615403	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs200911938	chr14:105615404-105615405	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs372399094	chr14:105615413-105615414	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142004780	chr14:105615422-105615423	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587752292	chr14:105615433-105615434	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs36024978	chr14:105615449-105615450	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs368900540	chr14:105615451-105615452	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs375459787	chr14:105615463-105615464	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs587684260	chr14:105615471-105615472	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs587740355	chr14:105615474-105615475	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs587621733	chr14:105615477-105615478	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs370004206	chr14:105615482-105615483	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374294516	chr14:105615495-105615496	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs377414264	chr14:105615504-105615505	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs368778866	chr14:105615514-105615515	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199566648	chr14:105615529-105615530	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs202068896	chr14:105615534-105615535	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374569282	chr14:105615543-105615544	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs150669646	chr14:105615593-105615594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
4	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
6	chr14:105607000-105615200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:105607000-105615400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr14:105607000-105618200	Strong transcription	Gastric	stomach
9	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:105607200-105616000	Strong transcription	HMEC	breast
11	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
12	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
13	chr14:105607600-105616000	Strong transcription	Fetal Intestine Small	intestine
14	chr14:105607600-105617600	Strong transcription	Skeletal Muscle Male	skeletal muscle
15	chr14:105607600-105625400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
17	chr14:105608000-105618000	Strong transcription	Adipose Nuclei	Adipose
18	chr14:105608200-105616400	Strong transcription	Right Ventricle	heart
19	chr14:105608800-105618400	Strong transcription	Lung	lung
20	chr14:105609000-105615000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:105609600-105618800	Weak transcription	Placenta	Placenta
23	chr14:105609600-105622000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
25	chr14:105610200-105625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:105611200-105615800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
27	chr14:105611800-105616000	Strong transcription	NHEK	skin
28	chr14:105612000-105615800	Strong transcription	Left Ventricle	heart
29	chr14:105612800-105615200	Strong transcription	A549	lung
30	chr14:105612800-105621000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:105613400-105615000	Weak transcription	Esophagus	oesophagus
32	chr14:105613400-105623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
34	chr14:105613600-105618400	Weak transcription	HSMMtube	muscle
35	chr14:105613600-105619200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr14:105613800-105615600	Strong transcription	Fetal Muscle Leg	muscle
38	chr14:105613800-105615800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr14:105613800-105616600	Weak transcription	Brain Germinal Matrix	brain
40	chr14:105613800-105616600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr14:105614000-105620200	Weak transcription	Fetal Brain Female	brain
43	chr14:105614000-105621600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:105614000-105622000	Weak transcription	Brain Hippocampus Middle	brain
45	chr14:105614200-105615400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:105614600-105616000	Genic enhancers	Spleen	Spleen
47	chr14:105614600-105619000	Strong transcription	Fetal Stomach	stomach
48	chr14:105614800-105616800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:105615000-105615200	ZNF genes & repeats	Esophagus	oesophagus
50	chr14:105615200-105615600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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