Variant report

Variant	esv3338795
Chromosome Location	chr13:111125251-111129449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:111127955-111128352	GM12878	blood:	n/a	n/a
2	ATF2	chr13:111127530-111128391	GM12878	blood:	n/a	n/a
3	BCL3	chr13:111126909-111127591	GM12878	blood:	n/a	n/a
4	BCL3	chr13:111126786-111127625	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:111126884-111127576	K562	blood:	n/a	n/a
6	BHLHE40	chr13:111127358-111127373	GM12878	blood:	n/a	n/a
7	BRCA1	chr13:111127223-111127240	GM12878	blood:	n/a	n/a
8	CEBPB	chr13:111127742-111128470	GM12878	blood:	n/a	n/a
9	CREB1	chr13:111127813-111128284	GM12878	blood:	n/a	n/a
10	CTCF	chr13:111127104-111127150	MCF-7	breast:	n/a	n/a
11	CTCF	chr13:111126955-111127123	GM12891	blood:	n/a	n/a
12	CTCF	chr13:111128401-111128467	GM12892	blood:	n/a	chr13:111128423-111128436
13	CTCF	chr13:111128318-111128559	K562	blood:	n/a	chr13:111128423-111128436 chr13:111128488-111128509
14	CTCF	chr13:111127056-111127177	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:111127096-111127162	NHEK	skin:	n/a	n/a
16	CTCF	chr13:111128371-111128474	GM12891	blood:	n/a	chr13:111128423-111128436
17	CTCF	chr13:111126920-111126935	GM12891	blood:	n/a	n/a
18	CTCF	chr13:111125900-111126050	WI-38	lung:	n/a	n/a
19	CTCF	chr13:111126858-111127460	GM19239	blood:	n/a	n/a
20	CTCF	chr13:111128340-111128490	HepG2	liver:	n/a	chr13:111128423-111128436
21	CTCF	chr13:111127126-111127129	GM12891	blood:	n/a	n/a
22	CTCF	chr13:111127146-111127206	MCF-7	breast:	n/a	n/a
23	CTCF	chr13:111127207-111127220	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:111128460-111128503	GM19238	blood:	n/a	n/a
25	CTCF	chr13:111126942-111126954	GM12891	blood:	n/a	n/a
26	CTCF	chr13:111127131-111127136	GM12891	blood:	n/a	n/a
27	CTCF	chr13:111127117-111127238	GM12892	blood:	n/a	n/a
28	CTCF	chr13:111128380-111128530	HepG2	liver:	n/a	chr13:111128423-111128436 chr13:111128488-111128509
29	CTCF	chr13:111128379-111128447	HepG2	liver:	n/a	chr13:111128423-111128436
30	CTCF	chr13:111128440-111128590	BE2_C	brain:	n/a	chr13:111128488-111128509
31	FOXM1	chr13:111127781-111128441	GM12878	blood:	n/a	n/a
32	FOXM1	chr13:111127739-111128372	GM12878	blood:	n/a	n/a
33	GATA2	chr13:111127417-111127686	SH-SY5Y	brain:	n/a	chr13:111127583-111127590 chr13:111127583-111127590 chr13:111127576-111127597 chr13:111127583-111127590
34	GATA3	chr13:111127489-111127761	SH-SY5Y	brain:	n/a	chr13:111127583-111127590 chr13:111127583-111127590 chr13:111127576-111127597 chr13:111127583-111127590
35	JUND	chr13:111127503-111127697	K562	blood:	n/a	n/a
36	MAFK	chr13:111127566-111127582	K562	blood:	n/a	n/a
37	MAX	chr13:111126878-111127334	NB4	blood:	n/a	chr13:111126934-111126944 chr13:111126984-111126994
38	MAX	chr13:111127070-111127640	K562	blood:	n/a	n/a
39	MAZ	chr13:111128314-111128484	K562	blood:	n/a	n/a
40	MEF2A	chr13:111127909-111128404	GM12878	blood:	n/a	chr13:111128187-111128202
41	MTA3	chr13:111127790-111128620	GM12878	blood:	n/a	n/a
42	MTA3	chr13:111124601-111125394	GM12878	blood:	n/a	n/a
43	MTA3	chr13:111127239-111128283	GM12878	blood:	n/a	n/a
44	MTA3	chr13:111126894-111127446	GM12878	blood:	n/a	n/a
45	MYC	chr13:111127398-111127613	K562	blood:	n/a	n/a
46	MYC	chr13:111127307-111127337	MCF-7	breast:	n/a	n/a
47	MYC	chr13:111126957-111127325	MCF-7	breast:	n/a	chr13:111126984-111126994
48	MYC	chr13:111127291-111127443	GM12878	blood:	n/a	n/a
49	MYC	chr13:111127124-111127147	MCF-7	breast:	n/a	n/a
50	MYC	chr13:111126989-111127376	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111128071-111128121	SKMC	muscle:	n/a
2	chr13:111127601-111127651	HMEC	breast:	n/a
3	chr13:111127601-111127651	SK-N-SH	brain:	n/a
4	chr13:111127505-111127555	HCPEpiC	choroid plexus:	n/a
5	chr13:111128054-111128104	RPTEC	kidney:	n/a
6	chr13:111127601-111127651	GM06990	blood:	n/a
7	chr13:111127601-111127651	SK-N-MC	brain:	n/a
8	chr13:111128054-111128104	HAEpiC	amniotic membrane:	n/a
9	chr13:111128102-111128152	SAEC	small airway:	n/a
10	chr13:111128071-111128121	Hela-S3	cervix:	n/a
11	chr13:111127601-111127651	HL-60	blood:	n/a
12	chr13:111127601-111127651	HPAEpiC	pulmonary alveolar:	n/a
13	chr13:111127505-111127555	NB4	blood:	n/a
14	chr13:111127601-111127651	PFSK-1	brain:	n/a
15	chr13:111128071-111128121	HRCEpiC	kidney:	n/a
16	chr13:111128071-111128121	U87	brain:	n/a
17	chr13:111128054-111128104	BE2_C	brain:	n/a
18	chr13:111128071-111128121	GM12878	blood:	n/a
19	chr13:111127601-111127651	U87	brain:	n/a
20	chr13:111127505-111127555	HCF	heart:	n/a
21	chr13:111128054-111128104	NH-A	brain:	n/a
22	chr13:111128102-111128152	GM19239	blood:	n/a
23	chr13:111127505-111127555	AG09309	skin:	n/a
24	chr13:111128071-111128121	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:111127505-111127555	SK-N-MC	brain:	n/a
26	chr13:111128054-111128104	IMR90	lung:	fetal
27	chr13:111127505-111127555	K562	blood:	n/a
28	chr13:111128102-111128152	PANC-1	pancreas:	n/a
29	chr13:111127601-111127651	HAEpiC	amniotic membrane:	n/a
30	chr13:111128071-111128121	MCF-7	breast:	n/a
31	chr13:111128071-111128121	IMR90	lung:	fetal
32	chr13:111127505-111127555	U87	brain:	n/a
33	chr13:111127601-111127651	CMK	blood:	n/a
34	chr13:111128071-111128121	AG04449	skin:	fetal
35	chr13:111128054-111128104	T-47D	breast:	n/a
36	chr13:111127505-111127555	MCF10A-Er-Src	breast:	n/a
37	chr13:111127601-111127651	MCF10A-Er-Src	breast:	n/a
38	chr13:111128102-111128152	MCF-7	breast:	n/a
39	chr13:111128071-111128121	GM19239	blood:	n/a
40	chr13:111128071-111128121	HRE	kidney:	n/a
41	chr13:111128054-111128104	PFSK-1	brain:	n/a
42	chr13:111128071-111128121	Jurkat	blood:	n/a
43	chr13:111128054-111128104	HEEpiC	esophagus:	n/a
44	chr13:111128054-111128104	NB4	blood:	n/a
45	chr13:111127505-111127555	BE2_C	brain:	n/a
46	chr13:111128071-111128121	HL-60	blood:	n/a
47	chr13:111127601-111127651	PrEC	prostate:	n/a
48	chr13:111128054-111128104	HRE	kidney:	n/a
49	chr13:111128071-111128121	Caco-2	colon:	n/a
50	chr13:111128054-111128104	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:111125375..111127376-chr13:111131017..111133682,2	K562	blood:
2	chr13:111123579..111125936-chr13:111162097..111164181,2	K562	blood:
3	chr13:111123294..111125798-chr13:111130475..111133407,2	K562	blood:

No data

Variant related genes	Relation type
COL4A2	TF binding region
COL4A2	CpG island

Extended variants
information (count: 236 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:236 , 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	rs377148815	chr13:111125291-111125292	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs564569125	chr13:111125304-111125305	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375548321	chr13:111125316-111125317	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs369694407	chr13:111125363-111125364	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369620826	chr13:111125403-111125404	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568478674	chr13:111125419-111125420	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529661399	chr13:111125423-111125424	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372356357	chr13:111125448-111125449	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs376694121	chr13:111125467-111125468	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs547810227	chr13:111125520-111125521	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs566552032	chr13:111125524-111125525	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533697981	chr13:111125550-111125551	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs558672337	chr13:111125551-111125552	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559542642	chr13:111125557-111125558	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570564684	chr13:111125558-111125559	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs9588178	chr13:111125576-111125577	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556522297	chr13:111125592-111125593	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11617206	chr13:111125606-111125607	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377585301	chr13:111125617-111125618	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189597954	chr13:111125620-111125621	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554246387	chr13:111125635-111125636	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369189516	chr13:111125698-111125699	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545982695	chr13:111125708-111125709	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs561628325	chr13:111125709-111125710	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs9588179	chr13:111125747-111125748	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531826777	chr13:111125762-111125763	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs547364241	chr13:111125766-111125767	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs543679162	chr13:111125771-111125772	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs567131338	chr13:111125831-111125832	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562022820	chr13:111125837-111125838	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs115261726	chr13:111125848-111125849	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547780261	chr13:111125861-111125862	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs9521796	chr13:111125933-111125934	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs180829249	chr13:111125934-111125935	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs7320419	chr13:111126023-111126024	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374509565	chr13:111126068-111126069	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538018782	chr13:111126076-111126077	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537901309	chr13:111126079-111126080	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376349006	chr13:111126109-111126110	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138230920	chr13:111126119-111126120	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554551740	chr13:111126170-111126171	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4773190	chr13:111126242-111126243	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs374195074	chr13:111126269-111126270	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149552303	chr13:111126279-111126280	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144289012	chr13:111126280-111126281	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9515232	chr13:111126303-111126304	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201805095	chr13:111126308-111126309	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs386380714	chr13:111126312-111126313	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561494308	chr13:111126316-111126317	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72519499	chr13:111126317-111126318	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
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
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	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
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111078200-111136800	Weak transcription	Colonic Mucosa	Colon
2	chr13:111101600-111130200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr13:111101800-111127800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr13:111103800-111125600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr13:111105800-111138000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr13:111107600-111130400	Weak transcription	Right Atrium	heart
7	chr13:111108200-111129200	Strong transcription	Right Ventricle	heart
8	chr13:111108200-111138400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr13:111108400-111126800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr13:111108600-111127000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:111108600-111138200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:111108600-111149200	Strong transcription	Fetal Stomach	stomach
13	chr13:111108600-111150600	Weak transcription	NHDF-Ad	bronchial
14	chr13:111108800-111126800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr13:111108800-111126800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr13:111108800-111126800	Weak transcription	Fetal Heart	heart
17	chr13:111108800-111126800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr13:111108800-111127000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr13:111108800-111130200	Strong transcription	Stomach Smooth Muscle	stomach
20	chr13:111108800-111148800	Weak transcription	Brain Angular Gyrus	brain
21	chr13:111108800-111152200	Strong transcription	Fetal Intestine Small	intestine
22	chr13:111109000-111126800	Weak transcription	A549	lung
23	chr13:111109000-111129200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:111109000-111158800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr13:111109600-111131000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr13:111109600-111155800	Strong transcription	Fetal Intestine Large	intestine
27	chr13:111109600-111158800	Strong transcription	Ovary	ovary
28	chr13:111109800-111126800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr13:111109800-111152600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:111109800-111168000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr13:111112000-111127000	Weak transcription	Esophagus	oesophagus
32	chr13:111113000-111126800	Strong transcription	Lung	lung
33	chr13:111114000-111131600	Strong transcription	Colon Smooth Muscle	Colon
34	chr13:111114200-111138800	Strong transcription	Aorta	Aorta
35	chr13:111116200-111130400	Weak transcription	Psoas Muscle	Psoas
36	chr13:111117200-111152000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr13:111117400-111127000	Strong transcription	Fetal Lung	lung
38	chr13:111117800-111130200	Strong transcription	Left Ventricle	heart
39	chr13:111118000-111127800	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr13:111118200-111129200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr13:111118800-111127000	Weak transcription	Fetal Brain Male	brain
42	chr13:111119000-111127200	Weak transcription	Brain Substantia Nigra	brain
43	chr13:111119000-111142600	Weak transcription	Stomach Mucosa	stomach
44	chr13:111119000-111143600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr13:111119200-111126800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr13:111119200-111138200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:111119200-111150400	Weak transcription	Brain Anterior Caudate	brain
48	chr13:111119200-111159200	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr13:111119600-111125600	Weak transcription	Brain Hippocampus Middle	brain
50	chr13:111119600-111129000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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