Variant report

Variant	esv1804050
Chromosome Location	chr13:98076911-98096882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:958)
CpG islands
(count:795)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:98088135-98088438	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:98085366-98086241	HepG2	liver:	n/a	n/a
3	ATF2	chr13:98085038-98086272	GM12878	blood:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
4	ATF2	chr13:98085096-98085777	H1-hESC	embryonic stem cell:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
5	ATF2	chr13:98085147-98086057	H1-hESC	embryonic stem cell:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
6	ATF2	chr13:98085304-98086176	GM12878	blood:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
7	ATF3	chr13:98085226-98085687	GM12878	blood:	n/a	chr13:98085404-98085424
8	ATF3	chr13:98085219-98085630	H1-hESC	embryonic stem cell:	n/a	chr13:98085404-98085424
9	ATF3	chr13:98086060-98086274	K562	blood:	n/a	n/a
10	BACH1	chr13:98085062-98085771	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr13:98086880-98086884	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr13:98088051-98088390	GM12878	blood:	n/a	n/a
13	BATF	chr13:98088019-98088387	GM12878	blood:	n/a	n/a
14	BCL3	chr13:98084855-98085657	A549	lung:	n/a	n/a
15	BCLAF1	chr13:98084876-98085864	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:98084588-98086514	GM12878	blood:	n/a	chr13:98085193-98085209
17	BHLHE40	chr13:98088016-98088399	GM12878	blood:	n/a	n/a
18	BHLHE40	chr13:98083830-98083878	K562	blood:	n/a	n/a
19	BHLHE40	chr13:98086852-98087065	K562	blood:	n/a	n/a
20	BHLHE40	chr13:98085211-98086183	K562	blood:	n/a	n/a
21	BHLHE40	chr13:98085153-98086201	HepG2	liver:	n/a	chr13:98085193-98085209
22	BHLHE40	chr13:98082020-98082280	HepG2	liver:	n/a	n/a
23	BHLHE40	chr13:98081971-98082315	K562	blood:	n/a	n/a
24	BRCA1	chr13:98085288-98085593	HepG2	liver:	n/a	n/a
25	BRCA1	chr13:98085482-98085634	GM12878	blood:	n/a	n/a
26	BRCA1	chr13:98085034-98085254	GM12878	blood:	n/a	n/a
27	BRCA1	chr13:98085978-98086076	GM12878	blood:	n/a	n/a
28	BRCA1	chr13:98085144-98086211	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr13:98085254-98085632	K562	blood:	n/a	n/a
30	CBX3	chr13:98085076-98085717	K562	blood:	n/a	n/a
31	CCNT2	chr13:98085530-98087217	K562	blood:	n/a	n/a
32	CEBPB	chr13:98078963-98079325	HepG2	liver:	n/a	chr13:98079122-98079133
33	CEBPB	chr13:98081808-98082253	Hela-S3	cervix:	n/a	chr13:98081990-98082001
34	CEBPB	chr13:98081818-98082167	K562	blood:	n/a	chr13:98081990-98082001
35	CEBPB	chr13:98081819-98082180	HepG2	liver:	n/a	chr13:98081990-98082001
36	CEBPB	chr13:98092897-98093350	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:98084807-98086028	IMR90	lung:	n/a	n/a
38	CEBPB	chr13:98085277-98086202	GM12878	blood:	n/a	n/a
39	CEBPB	chr13:98081913-98082069	K562	blood:	n/a	chr13:98081990-98082001
40	CEBPB	chr13:98081840-98082135	K562	blood:	n/a	chr13:98081990-98082001
41	CEBPB	chr13:98091589-98091815	HepG2	liver:	n/a	n/a
42	CEBPB	chr13:98081808-98082195	IMR90	lung:	n/a	chr13:98081990-98082001
43	CEBPB	chr13:98081826-98082176	A549	lung:	n/a	chr13:98081990-98082001
44	CEBPD	chr13:98086329-98086647	HepG2	liver:	n/a	n/a
45	CHD1	chr13:98084569-98086399	IMR90	lung:	n/a	n/a
46	CHD1	chr13:98085472-98086164	GM12878	blood:	n/a	n/a
47	CHD1	chr13:98085761-98086057	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr13:98086757-98087423	GM12878	blood:	n/a	n/a
49	CHD1	chr13:98084629-98085170	GM12878	blood:	n/a	n/a
50	CHD1	chr13:98087990-98088419	GM12878	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:98092033-98092083	HRCEpiC	kidney:	n/a
2	chr13:98085947-98085997	SKMC	muscle:	n/a
3	chr13:98092033-98092083	HRCEpiC	kidney:	n/a
4	chr13:98085947-98085997	SKMC	muscle:	n/a
5	chr13:98085949-98085999	AG04449	skin:	fetal
6	chr13:98086635-98086685	AoSMC	blood vessel:	n/a
7	chr13:98086635-98086685	GM06990	blood:	n/a
8	chr13:98085947-98085997	H1-hESC	embryonic stem cell:	embryo
9	chr13:98085375-98085425	H1-hESC	embryonic stem cell:	embryo
10	chr13:98086784-98086834	PrEC	prostate:	n/a
11	chr13:98092033-98092083	T-47D	breast:	n/a
12	chr13:98086635-98086685	BE2_C	brain:	n/a
13	chr13:98086784-98086834	Jurkat	blood:	n/a
14	chr13:98086433-98086483	NH-A	brain:	n/a
15	chr13:98086635-98086685	HMEC	breast:	n/a
16	chr13:98086427-98086477	T-47D	breast:	n/a
17	chr13:98090226-98090276	HIPEpiC	eye:	n/a
18	chr13:98092033-98092083	HL-60	blood:	n/a
19	chr13:98086635-98086685	HCM	heart:	n/a
20	chr13:98086784-98086834	LNCaP	prostate:	n/a
21	chr13:98084247-98084297	PANC-1	pancreas:	n/a
22	chr13:98085947-98085997	AG04449	skin:	fetal
23	chr13:98085463-98085513	SK-N-SH_RA	brain:	n/a
24	chr13:98090226-98090276	SK-N-MC	brain:	n/a
25	chr13:98085463-98085513	GM12878	blood:	n/a
26	chr13:98085375-98085425	AG10803	skin:	n/a
27	chr13:98092033-98092083	ovcar-3	ovarian:	n/a
28	chr13:98092033-98092083	NHBE	bronchial:	n/a
29	chr13:98085375-98085425	MCF-7	breast:	n/a
30	chr13:98087382-98087432	SK-N-MC	brain:	n/a
31	chr13:98082992-98083042	HepG2	liver:	n/a
32	chr13:98092033-98092083	HUVEC	blood vessel:	n/a
33	chr13:98086635-98086685	HEK293	kidney:	embryo
34	chr13:98085947-98085997	HEEpiC	esophagus:	n/a
35	chr13:98085947-98085997	GM12878	blood:	n/a
36	chr13:98084247-98084297	PFSK-1	brain:	n/a
37	chr13:98090226-98090276	HRPEpiC	eye:	n/a
38	chr13:98086784-98086834	PFSK-1	brain:	n/a
39	chr13:98085947-98085997	GM19239	blood:	n/a
40	chr13:98092033-98092083	HCPEpiC	choroid plexus:	n/a
41	chr13:98085463-98085513	PFSK-1	brain:	n/a
42	chr13:98085947-98085997	Jurkat	blood:	n/a
43	chr13:98084247-98084297	HMEC	breast:	n/a
44	chr13:98092033-98092083	K562	blood:	n/a
45	chr13:98085949-98085999	HEEpiC	esophagus:	n/a
46	chr13:98085375-98085425	LNCaP	prostate:	n/a
47	chr13:98085947-98085997	PANC-1	pancreas:	n/a
48	chr13:98085463-98085513	HRCEpiC	kidney:	n/a
49	chr13:98086427-98086477	A549	lung:	n/a
50	chr13:98085947-98085997	HMEC	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:98086365..98087880-chr13:98096785..98099178,2	MCF-7	breast:
2	chr13:98084712..98086856-chr13:98095176..98097332,2	K562	blood:
3	chr13:98085550..98088911-chr13:98089410..98093711,6	MCF-7	breast:
4	chr13:98070174..98073119-chr13:98075516..98077748,2	K562	blood:
5	chr13:98082222..98082861-chr20:60641074..60641593,2	NB4	blood:
6	chr13:98088366..98091907-chr13:98092585..98097383,6	K562	blood:
7	chr13:98071364..98074292-chr13:98079358..98081519,2	K562	blood:
8	chr13:98071956..98074377-chr13:98092594..98095295,2	K562	blood:
9	chr13:98078675..98081221-chr13:98083499..98086151,3	MCF-7	breast:
10	chr13:98093541..98095076-chr13:98218709..98220541,2	MCF-7	breast:
11	chr13:98092330..98094545-chr13:98105031..98106935,2	MCF-7	breast:
12	chr13:98078675..98081221-chr13:98083499..98086151,3	MCF-7	breast:
13	chr13:98072792..98075244-chr13:98079241..98080858,2	K562	blood:
14	chr13:98084623..98087568-chr13:98094102..98096230,2	MCF-7	breast:
15	chr13:98092292..98093986-chr13:98097522..98099677,2	K562	blood:
16	chr13:98084839..98085346-chr3:186764394..186765071,2	MCF-7	breast:
17	chr13:98085242..98089442-chr13:98089467..98091513,3	MCF-7	breast:
18	chr13:98080619..98083140-chr13:98084232..98086579,3	K562	blood:
19	chr13:98081401..98083229-chr13:98085571..98087258,2	MCF-7	breast:
20	chr13:98075639..98078018-chr13:98084903..98087132,2	K562	blood:
21	chr13:98088366..98091907-chr13:98092585..98097383,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OXGR1-6	chr13:98081597-98086236	NONHSAT034832

No data

Variant related genes	Relation type
RAP2A	TF binding region
RAP2A	CpG island
ENSG00000125249	chromatin interactions

Extended variants
information (count: 652 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2389907	chr13:98076911-98076912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377747897	chr13:98076984-98076985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550091833	chr13:98077116-98077117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548008762	chr13:98077139-98077140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs140992661	chr13:98077156-98077157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533812040	chr13:98077281-98077282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs559946080	chr13:98077336-98077337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553700980	chr13:98077389-98077390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs9582131	chr13:98077436-98077437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539350556	chr13:98077470-98077471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372760956	chr13:98077483-98077484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559071950	chr13:98077519-98077520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552776610	chr13:98077531-98077532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9554394	chr13:98077567-98077568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563203033	chr13:98077622-98077623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569771367	chr13:98077657-98077658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575770221	chr13:98077670-98077671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544668882	chr13:98077673-98077674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554798251	chr13:98077679-98077680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74105070	chr13:98077684-98077685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532027356	chr13:98077738-98077739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540274324	chr13:98077742-98077743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548332660	chr13:98077771-98077772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12865314	chr13:98077790-98077791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs112511525	chr13:98077815-98077816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182611383	chr13:98077826-98077827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187265700	chr13:98077827-98077828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117191584	chr13:98077896-98077897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547876232	chr13:98077900-98077901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144997263	chr13:98077914-98077915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs74242929	chr13:98077980-98077981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568111622	chr13:98078032-98078033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189824195	chr13:98078047-98078048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183003386	chr13:98078051-98078052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547374699	chr13:98078111-98078112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187611932	chr13:98078118-98078119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539310804	chr13:98078136-98078137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559013801	chr13:98078171-98078172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371665900	chr13:98078179-98078180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569414581	chr13:98078196-98078197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374129085	chr13:98078206-98078207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538094722	chr13:98078226-98078227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555041624	chr13:98078258-98078259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574554084	chr13:98078270-98078271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534045163	chr13:98078296-98078297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577988959	chr13:98078332-98078333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553724810	chr13:98078430-98078431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193228696	chr13:98078453-98078454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs61086335	chr13:98078469-98078470	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs185622634	chr13:98078630-98078631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21785460	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:98075800-98077800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr13:98076000-98081800	Weak transcription	HSMM	muscle
3	chr13:98076400-98077200	Enhancers	Brain Hippocampus Middle	brain
4	chr13:98076400-98077400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr13:98076400-98078000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr13:98076400-98081200	Weak transcription	Brain Angular Gyrus	brain
7	chr13:98076400-98081600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:98076400-98081600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr13:98076400-98081600	Weak transcription	Brain Substantia Nigra	brain
10	chr13:98076400-98081800	Weak transcription	Fetal Heart	heart
11	chr13:98076400-98081800	Weak transcription	Psoas Muscle	Psoas
12	chr13:98076400-98081800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr13:98076400-98081800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr13:98076400-98081800	Weak transcription	NHDF-Ad	bronchial
15	chr13:98076400-98081800	Weak transcription	Osteobl	bone
16	chr13:98076400-98084800	Weak transcription	Esophagus	oesophagus
17	chr13:98076600-98081000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr13:98076600-98081800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr13:98076800-98077000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr13:98077200-98078800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr13:98077200-98081600	Weak transcription	Brain Hippocampus Middle	brain
22	chr13:98077400-98078000	Enhancers	Brain Cingulate Gyrus	brain
23	chr13:98077800-98078200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr13:98078000-98078200	Enhancers	Brain Anterior Caudate	brain
25	chr13:98078000-98078600	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr13:98078000-98081000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr13:98078200-98081200	Weak transcription	Brain Anterior Caudate	brain
28	chr13:98078200-98081600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr13:98078600-98081000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr13:98078800-98079000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr13:98078800-98079200	Enhancers	HepG2	liver
32	chr13:98079000-98079200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr13:98079000-98079400	Enhancers	Liver	Liver
34	chr13:98079200-98079400	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr13:98079200-98081800	Weak transcription	HepG2	liver
36	chr13:98079400-98081200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr13:98079400-98084200	Weak transcription	Liver	Liver
38	chr13:98080000-98080200	Enhancers	Dnd41	blood
39	chr13:98080200-98080400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr13:98080200-98081000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr13:98080200-98081200	Weak transcription	Dnd41	blood
42	chr13:98080400-98084400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr13:98080600-98081000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:98080800-98081600	Enhancers	Brain Germinal Matrix	brain
45	chr13:98081000-98081200	Enhancers	Brain Cingulate Gyrus	brain
46	chr13:98081000-98081200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr13:98081000-98081800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr13:98081000-98081800	Enhancers	Fetal Brain Male	brain
49	chr13:98081000-98083800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr13:98081000-98084000	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links