Variant report

Variant	nsv832786
Chromosome Location	chr14:46279053-46427777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:561)
CpG islands
(count:306)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
4	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
5	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
7	BATF	chr14:46368023-46368235	GM12878	blood:	n/a	n/a
8	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
9	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
10	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
11	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
12	BCL11A	chr14:46338183-46338481	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:46337580-46337867	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:46337474-46337979	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
16	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
17	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
18	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
21	CEBPB	chr14:46388459-46388948	MCF-7	breast:	n/a	chr14:46388709-46388720
22	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
23	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr14:46388540-46388897	IMR90	lung:	n/a	chr14:46388709-46388720
25	CEBPB	chr14:46388507-46388949	MCF-7	breast:	n/a	chr14:46388709-46388720
26	CEBPB	chr14:46388556-46388893	A549	lung:	n/a	chr14:46388709-46388720
27	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
28	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
29	CEBPB	chr14:46309406-46309962	A549	lung:	n/a	chr14:46309800-46309811
30	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
31	CREB1	chr14:46337522-46338032	GM12878	blood:	n/a	n/a
32	CTCF	chr14:46399900-46399971	GM13976	blood:	n/a	n/a
33	CTCF	chr14:46307960-46308110	GM12873	blood:	n/a	chr14:46307991-46308009 chr14:46307993-46308014
34	CTCF	chr14:46279440-46279590	NHEK	skin:	n/a	n/a
35	CTCF	chr14:46279800-46279950	HMEC	breast:	n/a	n/a
36	CTCF	chr14:46308009-46308027	HepG2	liver:	n/a	n/a
37	CTCF	chr14:46279820-46279970	GM12873	blood:	n/a	n/a
38	CTCF	chr14:46340382-46340386	HepG2	liver:	n/a	n/a
39	CTCF	chr14:46409620-46409770	BE2_C	brain:	n/a	n/a
40	CTCF	chr14:46409506-46409974	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:46279800-46279950	HAc	cerebellar:	n/a	n/a
42	CTCF	chr14:46340320-46340470	GM12871	blood:	n/a	n/a
43	CTCF	chr14:46340240-46340390	GM12864	blood:	n/a	n/a
44	CTCF	chr14:46409440-46409590	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:46340300-46340450	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:46340340-46340490	GM12864	blood:	n/a	n/a
47	CTCF	chr14:46409740-46409890	RPTEC	kidney:	n/a	n/a
48	CTCF	chr14:46279800-46279950	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr14:46307900-46308050	SAEC	small airway:	n/a	chr14:46307991-46308009 chr14:46307993-46308014
50	CTCF	chr14:46279746-46279994	T-47D	breast:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46283117-46283167	SAEC	small airway:	n/a
2	chr14:46283117-46283167	SAEC	small airway:	n/a
3	chr14:46283117-46283167	BJ	skin:	n/a
4	chr14:46283117-46283167	LNCaP	prostate:	n/a
5	chr14:46283117-46283167	MCF-7	breast:	n/a
6	chr14:46300358-46300408	HIPEpiC	eye:	n/a
7	chr14:46300358-46300408	MCF-7	breast:	n/a
8	chr14:46283117-46283167	H1-hESC	embryonic stem cell:	embryo
9	chr14:46300358-46300408	NB4	blood:	n/a
10	chr14:46358279-46358329	BE2_C	brain:	n/a
11	chr14:46358279-46358329	HEK293	kidney:	embryo
12	chr14:46300358-46300408	HRPEpiC	eye:	n/a
13	chr14:46358139-46358189	HMEC	breast:	n/a
14	chr14:46283172-46283222	NH-A	brain:	n/a
15	chr14:46358279-46358329	NT2-D1	testis:	n/a
16	chr14:46283172-46283222	AoSMC	blood vessel:	n/a
17	chr14:46283172-46283222	Jurkat	blood:	n/a
18	chr14:46283172-46283222	HCM	heart:	n/a
19	chr14:46358279-46358329	H1-hESC	embryonic stem cell:	embryo
20	chr14:46358139-46358189	HCM	heart:	n/a
21	chr14:46300358-46300408	SK-N-SH_RA	brain:	n/a
22	chr14:46283172-46283222	HNPCEpiC	eye:	n/a
23	chr14:46358279-46358329	HUVEC	blood vessel:	n/a
24	chr14:46283172-46283222	NT2-D1	testis:	n/a
25	chr14:46283117-46283167	ovcar-3	ovarian:	n/a
26	chr14:46283117-46283167	HIPEpiC	eye:	n/a
27	chr14:46358139-46358189	HEEpiC	esophagus:	n/a
28	chr14:46358139-46358189	SK-N-SH	brain:	n/a
29	chr14:46358279-46358329	HCM	heart:	n/a
30	chr14:46300358-46300408	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:46358139-46358189	HEK293	kidney:	embryo
32	chr14:46283172-46283222	IMR90	lung:	fetal
33	chr14:46300358-46300408	IMR90	lung:	fetal
34	chr14:46300358-46300408	ovcar-3	ovarian:	n/a
35	chr14:46300358-46300408	HL-60	blood:	n/a
36	chr14:46283172-46283222	SKMC	muscle:	n/a
37	chr14:46283172-46283222	HCPEpiC	choroid plexus:	n/a
38	chr14:46283172-46283222	CMK	blood:	n/a
39	chr14:46283117-46283167	NHBE	bronchial:	n/a
40	chr14:46283172-46283222	ECC-1	luminal epithelium:	n/a
41	chr14:46358279-46358329	AG09319	gingival:	n/a
42	chr14:46283117-46283167	PrEC	prostate:	n/a
43	chr14:46358139-46358189	HCF	heart:	n/a
44	chr14:46358139-46358189	CMK	blood:	n/a
45	chr14:46283172-46283222	ovcar-3	ovarian:	n/a
46	chr14:46358279-46358329	HAEpiC	amniotic membrane:	n/a
47	chr14:46283117-46283167	HMEC	breast:	n/a
48	chr14:46358139-46358189	LNCaP	prostate:	n/a
49	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
50	chr14:46283117-46283167	GM12878	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
2	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
3	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
4	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
5	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
6	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
7	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
8	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
9	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
10	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
11	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
12	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
13	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
14	chr12:122908054..122908892-chr14:46408991..46409734,2	MCF-7	breast:
15	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
16	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46410146-46410221	ENSG00000258700
2	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
3	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675

No data

Variant related genes	Relation type
ENSG00000264420	TF binding region
LINC00871	TF binding region
ENSG00000264420	CpG island
LINC00871	CpG island

Extended variants
information (count: 1872 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1872 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529840927	chr14:46279077-46279078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539091069	chr14:46279092-46279093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148425787	chr14:46279182-46279183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561567971	chr14:46279202-46279203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142586605	chr14:46279203-46279204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547227312	chr14:46279219-46279220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571860313	chr14:46279284-46279285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558953946	chr14:46279290-46279291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565925059	chr14:46279336-46279337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146423053	chr14:46279352-46279353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550583633	chr14:46279389-46279390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140754097	chr14:46279471-46279472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10483584	chr14:46279473-46279474	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187704951	chr14:46279489-46279490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144612000	chr14:46279493-46279494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533755007	chr14:46279500-46279501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146868874	chr14:46279514-46279515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116609779	chr14:46279528-46279529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140628783	chr14:46279541-46279542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556226884	chr14:46279592-46279593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574572582	chr14:46279600-46279601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541953575	chr14:46279662-46279663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554939482	chr14:46279667-46279668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75874068	chr14:46279687-46279688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573346763	chr14:46279694-46279695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35109221	chr14:46279697-46279698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116480569	chr14:46279745-46279746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192637434	chr14:46279746-46279747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150451674	chr14:46279755-46279756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138294342	chr14:46279780-46279781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183517413	chr14:46279796-46279797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149587435	chr14:46279816-46279817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200868034	chr14:46279846-46279847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377722405	chr14:46279849-46279850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35789172	chr14:46279851-46279852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143264903	chr14:46279891-46279892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551936124	chr14:46279918-46279919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs137899461	chr14:46279939-46279940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139152152	chr14:46279945-46279946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187808845	chr14:46279955-46279956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552113797	chr14:46279964-46279965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142964956	chr14:46280009-46280010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568939809	chr14:46280021-46280022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192335230	chr14:46280161-46280162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35442619	chr14:46280201-46280202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs67267417	chr14:46280240-46280241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs574440810	chr14:46280246-46280247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80195399	chr14:46280251-46280252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147462993	chr14:46280272-46280273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140802158	chr14:46280315-46280316	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46277000-46279200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr14:46277400-46279200	Weak transcription	Fetal Heart	heart
3	chr14:46277800-46279800	Enhancers	Stomach Mucosa	stomach
4	chr14:46278200-46279400	Weak transcription	GM12878-XiMat	blood
5	chr14:46278200-46280600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:46278400-46279400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:46278400-46279400	Weak transcription	HMEC	breast
8	chr14:46278600-46279200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:46278800-46280400	Enhancers	Colon Smooth Muscle	Colon
10	chr14:46278800-46280800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:46279000-46280800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr14:46279000-46281200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr14:46279200-46280000	Enhancers	Fetal Lung	lung
14	chr14:46279200-46280200	Enhancers	Fetal Heart	heart
15	chr14:46279200-46280600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:46279200-46280600	Enhancers	Rectal Smooth Muscle	rectum
17	chr14:46279200-46280800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr14:46279400-46279600	Enhancers	GM12878-XiMat	blood
19	chr14:46279400-46279800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:46279400-46279800	Enhancers	Primary hematopoietic stem cells	blood
21	chr14:46279400-46279800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:46279400-46280000	Enhancers	HMEC	breast
23	chr14:46279400-46280200	Enhancers	NHEK	skin
24	chr14:46279400-46280600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:46279600-46280000	Weak transcription	GM12878-XiMat	blood
26	chr14:46280000-46280400	Enhancers	GM12878-XiMat	blood
27	chr14:46280200-46280800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:46287200-46289600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr14:46306400-46306800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr14:46306800-46307800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr14:46307800-46308800	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr14:46308000-46308600	Enhancers	Fetal Brain Male	brain
33	chr14:46308200-46308600	Enhancers	GM12878-XiMat	blood
34	chr14:46309200-46310000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:46315200-46316600	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr14:46333600-46334600	Active TSS	GM12878-XiMat	blood
37	chr14:46334600-46334800	Flanking Active TSS	GM12878-XiMat	blood
38	chr14:46334800-46335000	Active TSS	GM12878-XiMat	blood
39	chr14:46335000-46335600	Enhancers	GM12878-XiMat	blood
40	chr14:46335600-46335800	Flanking Active TSS	GM12878-XiMat	blood
41	chr14:46335600-46336200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:46335800-46336000	Enhancers	GM12878-XiMat	blood
43	chr14:46336000-46336200	Flanking Active TSS	GM12878-XiMat	blood
44	chr14:46336200-46336400	Active TSS	GM12878-XiMat	blood
45	chr14:46336200-46336800	Enhancers	Fetal Heart	heart
46	chr14:46336200-46338600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:46336400-46336600	Flanking Active TSS	GM12878-XiMat	blood
48	chr14:46336600-46337000	Active TSS	GM12878-XiMat	blood
49	chr14:46337000-46337600	Flanking Active TSS	GM12878-XiMat	blood
50	chr14:46337600-46337800	Enhancers	GM12878-XiMat	blood

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