Variant report

Variant	nsv2599
Chromosome Location	chr1:119935023-119967748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:119939742-119939798	K562	blood:	n/a	n/a
2	CTCF	chr1:119963380-119963530	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
3	CTCF	chr1:119963220-119963370	NHEK	skin:	n/a	n/a
4	CTCF	chr1:119963480-119963630	HBMEC	blood vessel:	n/a	n/a
5	CTCF	chr1:119963400-119963550	RPTEC	kidney:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
6	CTCF	chr1:119963380-119963530	HCM	heart:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
7	CTCF	chr1:119963389-119963511	GM12892	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
8	CTCF	chr1:119963360-119963510	HEEpiC	esophagus:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
9	CTCF	chr1:119963340-119963490	HPAF	blood vessel:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
10	CTCF	chr1:119952460-119952610	GM12866	blood:	n/a	n/a
11	CTCF	chr1:119948080-119948230	GM12869	blood:	n/a	n/a
12	CTCF	chr1:119965134-119965258	Lung_OC	lung:	n/a	n/a
13	CTCF	chr1:119963500-119963650	GM12865	blood:	n/a	n/a
14	CTCF	chr1:119963340-119963490	AG09319	gingival:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
15	CTCF	chr1:119963418-119963513	HepG2	liver:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
16	CTCF	chr1:119963373-119963537	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
17	CTCF	chr1:119963380-119963530	NHEK	skin:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
18	CTCF	chr1:119963377-119963542	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
19	CTCF	chr1:119963340-119963490	GM12878	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
20	CTCF	chr1:119963360-119963510	HMEC	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
21	CTCF	chr1:119952800-119952950	GM12868	blood:	n/a	n/a
22	CTCF	chr1:119963380-119963510	Gliobla	brain:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
23	CTCF	chr1:119963367-119963568	GM19239	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
24	CTCF	chr1:119963392-119963502	GM12878	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
25	CTCF	chr1:119963360-119963510	GM12873	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
26	CTCF	chr1:119963390-119963519	HepG2	liver:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
27	CTCF	chr1:119963386-119963530	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
28	CTCF	chr1:119963348-119963578	GM19240	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
29	CTCF	chr1:119963380-119963517	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
30	CTCF	chr1:119950648-119950699	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:119963368-119963562	MCF-7	breast:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
32	CTCF	chr1:119963500-119963650	HMEC	breast:	n/a	n/a
33	CTCF	chr1:119963400-119963550	HepG2	liver:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
34	CTCF	chr1:119963398-119963623	H1-hESC	embryonic stem cell:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
35	CTCF	chr1:119963375-119963520	H1-hESC	embryonic stem cell:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
36	CTCF	chr1:119963380-119963530	GM12871	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
37	CTCF	chr1:119963393-119963501	K562	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
38	CTCF	chr1:119963432-119963495	Hela-S3	cervix:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
39	CTCF	chr1:119963340-119963490	HEK293	kidney:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
40	CTCF	chr1:119963399-119963514	GM12891	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
41	CTCF	chr1:119963410-119963502	Fibrobl	skin:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
42	CTCF	chr1:119963380-119963530	SAEC	small airway:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
43	CTCF	chr1:119963375-119963548	NHEK	skin:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
44	CTCF	chr1:119963412-119963503	A549	lung:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
45	CTCF	chr1:119963395-119963508	GM19238	blood:	n/a	chr1:119963463-119963479 chr1:119963464-119963485 chr1:119963462-119963480
46	EP300	chr1:119939662-119939771	K562	blood:	n/a	n/a
47	FOXA1	chr1:119935981-119936304	HepG2	liver:	n/a	n/a
48	FOXA2	chr1:119936065-119936265	HepG2	liver:	n/a	n/a
49	GATA3	chr1:119935988-119936460	MCF-7	breast:	n/a	chr1:119936091-119936103
50	HCFC1	chr1:119939783-119939929	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:119957380-119957430	PANC-1	pancreas:	n/a
2	chr1:119958041-119958091	LNCaP	prostate:	n/a
3	chr1:119958041-119958091	U87	brain:	n/a
4	chr1:119957969-119958019	IMR90	lung:	fetal
5	chr1:119960007-119960057	Jurkat	blood:	n/a
6	chr1:119960007-119960057	ovcar-3	ovarian:	n/a
7	chr1:119957969-119958019	Caco-2	colon:	n/a
8	chr1:119957969-119958019	AG04449	skin:	fetal
9	chr1:119957969-119958019	SAEC	small airway:	n/a
10	chr1:119957969-119958019	PrEC	prostate:	n/a
11	chr1:119960007-119960057	AG10803	skin:	n/a
12	chr1:119957380-119957430	HEK293	kidney:	embryo
13	chr1:119957380-119957430	U87	brain:	n/a
14	chr1:119958041-119958091	AG09319	gingival:	n/a
15	chr1:119960007-119960057	BJ	skin:	n/a
16	chr1:119957380-119957430	SK-N-MC	brain:	n/a
17	chr1:119960007-119960057	HEK293	kidney:	embryo
18	chr1:119960007-119960057	HCM	heart:	n/a
19	chr1:119958041-119958091	GM19239	blood:	n/a
20	chr1:119957380-119957430	NT2-D1	testis:	n/a
21	chr1:119957380-119957430	BE2_C	brain:	n/a
22	chr1:119957380-119957430	HCM	heart:	n/a
23	chr1:119958041-119958091	HCF	heart:	n/a
24	chr1:119957969-119958019	SK-N-MC	brain:	n/a
25	chr1:119957380-119957430	PFSK-1	brain:	n/a
26	chr1:119960007-119960057	SKMC	muscle:	n/a
27	chr1:119960007-119960057	RPTEC	kidney:	n/a
28	chr1:119957969-119958019	HCF	heart:	n/a
29	chr1:119957969-119958019	HL-60	blood:	n/a
30	chr1:119957380-119957430	AG04449	skin:	fetal
31	chr1:119957969-119958019	HepG2	liver:	n/a
32	chr1:119958041-119958091	HRE	kidney:	n/a
33	chr1:119960007-119960057	HUVEC	blood vessel:	n/a
34	chr1:119958041-119958091	MCF-7	breast:	n/a
35	chr1:119958041-119958091	SK-N-MC	brain:	n/a
36	chr1:119957380-119957430	HRE	kidney:	n/a
37	chr1:119958041-119958091	K562	blood:	n/a
38	chr1:119958041-119958091	BJ	skin:	n/a
39	chr1:119957380-119957430	IMR90	lung:	fetal
40	chr1:119958041-119958091	NH-A	brain:	n/a
41	chr1:119958041-119958091	AG04449	skin:	fetal
42	chr1:119960007-119960057	SK-N-SH_RA	brain:	n/a
43	chr1:119957380-119957430	K562	blood:	n/a
44	chr1:119958041-119958091	NB4	blood:	n/a
45	chr1:119957969-119958019	HEEpiC	esophagus:	n/a
46	chr1:119957969-119958019	BJ	skin:	n/a
47	chr1:119957969-119958019	HRCEpiC	kidney:	n/a
48	chr1:119960007-119960057	U87	brain:	n/a
49	chr1:119957380-119957430	BJ	skin:	n/a
50	chr1:119960007-119960057	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:119937462..119940451-chr17:57969185..57971965,2	MCF-7	breast:
2	chr1:119967296..119969722-chr1:119972549..119974049,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD3B2-1	chr1:119952263-119952538	ENSG00000249401
2	lnc-HSD3B2-3	chr1:119935062-119935310	NONHSAT005566
3	lnc-HSD3B2-3	chr1:119936408-119936737	NONHSAT005566

Variant related genes	Relation type
HAO2	TF binding region
HSD3B2	TF binding region
HAO2	CpG island
HSD3B2	CpG island
ENSG00000108423	chromatin interactions
ENSG00000108443	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 1176 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191079489	chr1:119935035-119935036	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587758489	chr1:119935037-119935038	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587633660	chr1:119935038-119935039	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376645949	chr1:119935047-119935048	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2275608	chr1:119935061-119935062	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183293054	chr1:119935120-119935121	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs75633256	chr1:119935133-119935134	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs587620780	chr1:119935135-119935136	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs587684257	chr1:119935136-119935137	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs587760684	chr1:119935187-119935188	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs373025356	chr1:119935192-119935193	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs376061942	chr1:119935216-119935217	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs200829935	chr1:119935280-119935281	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs370380040	chr1:119935283-119935284	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs372655209	chr1:119935289-119935290	Genic enhancers Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs376954402	chr1:119935312-119935313	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370068717	chr1:119935320-119935321	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74575149	chr1:119935321-119935322	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368560652	chr1:119935335-119935336	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188223185	chr1:119935336-119935337	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199981951	chr1:119935341-119935342	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587712435	chr1:119935394-119935395	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193128553	chr1:119935400-119935401	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139001921	chr1:119935404-119935405	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373215821	chr1:119935407-119935408	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587661689	chr1:119935437-119935438	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587725111	chr1:119935452-119935453	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587600362	chr1:119935467-119935468	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587678775	chr1:119935503-119935504	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10802092	chr1:119935507-119935508	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs587635493	chr1:119935530-119935531	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74114308	chr1:119935543-119935544	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs587724239	chr1:119935552-119935553	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587628193	chr1:119935569-119935570	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182975139	chr1:119935570-119935571	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587765483	chr1:119935571-119935572	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587628729	chr1:119935577-119935578	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11582039	chr1:119935589-119935590	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587685779	chr1:119935619-119935620	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149478927	chr1:119935702-119935703	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587638741	chr1:119935706-119935707	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112225619	chr1:119935711-119935712	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143065896	chr1:119935718-119935719	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148198231	chr1:119935762-119935763	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587648211	chr1:119935822-119935823	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74114309	chr1:119935824-119935825	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187693809	chr1:119935825-119935826	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587677134	chr1:119935830-119935831	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587733693	chr1:119935846-119935847	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376090037	chr1:119935901-119935902	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119932600-119937000	Enhancers	Fetal Intestine Small	intestine
2	chr1:119933000-119935400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:119933200-119937000	Genic enhancers	Liver	Liver
4	chr1:119934000-119937600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:119935000-119936000	Weak transcription	Fetal Intestine Large	intestine
6	chr1:119935400-119937600	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr1:119936000-119936400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr1:119936000-119940800	Enhancers	Fetal Intestine Large	intestine
9	chr1:119936200-119937800	Enhancers	HepG2	liver
10	chr1:119936400-119937000	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr1:119937000-119937400	Weak transcription	Fetal Intestine Small	intestine
12	chr1:119937000-119937600	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr1:119937000-119945800	Weak transcription	Liver	Liver
14	chr1:119937400-119938000	Enhancers	Fetal Intestine Small	intestine
15	chr1:119937600-119937800	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr1:119937800-119938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:119937800-119946400	Weak transcription	HepG2	liver
18	chr1:119938000-119939000	Weak transcription	Fetal Intestine Small	intestine
19	chr1:119938200-119938600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr1:119939000-119941600	Enhancers	Fetal Intestine Small	intestine
21	chr1:119939400-119940600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:119940800-119941400	Weak transcription	Fetal Intestine Large	intestine
23	chr1:119941400-119941600	Enhancers	Fetal Intestine Large	intestine
24	chr1:119946400-119946800	Enhancers	HepG2	liver
25	chr1:119946400-119948200	ZNF genes & repeats	Liver	Liver
26	chr1:119947000-119948000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:119947600-119947800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:119948000-119950200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:119952000-119952400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr1:119952200-119953600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:119952200-119953800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:119953000-119954400	Enhancers	Fetal Intestine Large	intestine
33	chr1:119953400-119954200	Enhancers	Fetal Intestine Small	intestine
34	chr1:119953800-119954200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr1:119954400-119955600	Weak transcription	Fetal Intestine Large	intestine
36	chr1:119955600-119956000	Enhancers	Fetal Intestine Large	intestine
37	chr1:119956000-119962200	Weak transcription	Fetal Intestine Large	intestine
38	chr1:119957200-119958000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr1:119957400-119958200	Enhancers	Pancreas	Pancrea
40	chr1:119958200-119959800	Enhancers	Liver	Liver
41	chr1:119959800-119961400	Weak transcription	Liver	Liver
42	chr1:119961400-119963600	Enhancers	Liver	Liver
43	chr1:119962200-119963800	Enhancers	Fetal Intestine Large	intestine
44	chr1:119965800-119966200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr1:119966000-119966400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr1:119966000-119966800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr1:119966000-119967200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:119967200-119970000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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