Variant report

Variant	nsv1046582
Chromosome Location	chr10:43167074-43214053
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	ARID3A	chr10:43175769-43175936	K562	blood:	n/a	n/a
2	ATF1	chr10:43180091-43180303	K562	blood:	n/a	n/a
3	CEBPB	chr10:43195023-43195204	K562	blood:	n/a	n/a
4	CEBPB	chr10:43175714-43176099	K562	blood:	n/a	chr10:43175919-43175930
5	CEBPB	chr10:43204367-43204575	HepG2	liver:	n/a	chr10:43204513-43204524 chr10:43204512-43204525
6	CEBPB	chr10:43169636-43169884	K562	blood:	n/a	n/a
7	CEBPB	chr10:43175770-43176061	A549	lung:	n/a	chr10:43175919-43175930
8	CEBPB	chr10:43175734-43176194	K562	blood:	n/a	chr10:43175919-43175930
9	CEBPB	chr10:43175782-43176201	HepG2	liver:	n/a	chr10:43175919-43175930
10	CTCF	chr10:43186100-43186250	WERI-Rb-1	eye:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
11	CTCF	chr10:43186100-43186250	HEK293	kidney:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
12	CTCF	chr10:43185820-43185970	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr10:43186180-43186330	HEK293	kidney:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
14	CTCF	chr10:43186108-43186272	H1-hESC	embryonic stem cell:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
15	CTCF	chr10:43185990-43185994	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:43186049-43186326	GM12878	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
17	CTCF	chr10:43202700-43202850	Caco-2	colon:	n/a	n/a
18	CTCF	chr10:43186784-43187085	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr10:43186107-43186267	Hela-S3	cervix:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
20	CTCF	chr10:43207580-43207595	GM13976	blood:	n/a	n/a
21	CTCF	chr10:43185859-43186469	MCF-7	breast:	n/a	chr10:43186347-43186360 chr10:43186191-43186209 chr10:43186193-43186214
22	CTCF	chr10:43189850-43189903	Lung_OC	lung:	n/a	n/a
23	CTCF	chr10:43202780-43202930	Caco-2	colon:	n/a	chr10:43202853-43202874 chr10:43202859-43202875 chr10:43202858-43202876
24	CTCF	chr10:43186074-43186283	K562	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
25	CTCF	chr10:43186120-43186270	SK-N-SH_RA	brain:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
26	CTCF	chr10:43186161-43186225	GM12891	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
27	CTCF	chr10:43185800-43185950	HepG2	liver:	n/a	n/a
28	CTCF	chr10:43186120-43186270	NB4	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
29	CTCF	chr10:43170893-43170909	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr10:43186060-43186210	GM12872	blood:	n/a	chr10:43186191-43186209
31	CTCF	chr10:43186160-43186310	GM12873	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
32	CTCF	chr10:43185840-43185990	HepG2	liver:	n/a	n/a
33	CTCF	chr10:43186015-43186310	MCF-7	breast:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
34	CTCF	chr10:43185945-43186315	MCF-7	breast:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
35	CTCF	chr10:43186120-43186270	HepG2	liver:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
36	CTCF	chr10:43186080-43186230	K562	blood:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
37	CTCF	chr10:43185995-43186326	MCF-7	breast:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
38	CTCF	chr10:43186045-43186260	HepG2	liver:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
39	CTCF	chr10:43201282-43201346	GM10266	blood:	n/a	n/a
40	CTCF	chr10:43186070-43186305	HepG2	liver:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
41	CTCF	chr10:43214038-43214096	GM13976	blood:	n/a	n/a
42	CTCF	chr10:43186141-43186241	NHEK	skin:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
43	CTCF	chr10:43202793-43202927	Pancreas_OC	pancreas:	n/a	chr10:43202853-43202874 chr10:43202859-43202875 chr10:43202858-43202876
44	CTCF	chr10:43186088-43186297	SK-N-SH_RA	brain:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
45	CTCF	chr10:43185925-43186326	MCF-7	breast:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
46	CTCF	chr10:43186160-43186310	A549	lung:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
47	CTCF	chr10:43194130-43194228	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr10:43186054-43186283	SK-N-SH_RA	brain:	n/a	chr10:43186191-43186209 chr10:43186193-43186214
49	CTCF	chr10:43186831-43187008	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:43186066-43186279	Gliobla	brain:	n/a	chr10:43186191-43186209 chr10:43186193-43186214

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43187184-43187234	BE2_C	brain:	n/a
2	chr10:43187184-43187234	AoSMC	blood vessel:	n/a
3	chr10:43187184-43187234	BE2_C	brain:	n/a
4	chr10:43187184-43187234	AoSMC	blood vessel:	n/a
5	chr10:43187184-43187234	HEEpiC	esophagus:	n/a
6	chr10:43186900-43186950	AG04450	lung:	fetal
7	chr10:43187469-43187519	Jurkat	blood:	n/a
8	chr10:43209934-43209984	HMEC	breast:	n/a
9	chr10:43186900-43186950	HCPEpiC	choroid plexus:	n/a
10	chr10:43187175-43187225	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:43209934-43209984	GM12892	blood:	n/a
12	chr10:43187469-43187519	MCF10A-Er-Src	breast:	n/a
13	chr10:43187175-43187225	BJ	skin:	n/a
14	chr10:43186868-43186918	HIPEpiC	eye:	n/a
15	chr10:43186810-43186860	GM12892	blood:	n/a
16	chr10:43186900-43186950	HMEC	breast:	n/a
17	chr10:43187175-43187225	HepG2	liver:	n/a
18	chr10:43187469-43187519	SK-N-MC	brain:	n/a
19	chr10:43187184-43187234	BJ	skin:	n/a
20	chr10:43186810-43186860	NT2-D1	testis:	n/a
21	chr10:43186868-43186918	T-47D	breast:	n/a
22	chr10:43187175-43187225	PANC-1	pancreas:	n/a
23	chr10:43187175-43187225	SK-N-SH	brain:	n/a
24	chr10:43209934-43209984	SKMC	muscle:	n/a
25	chr10:43187469-43187519	HMEC	breast:	n/a
26	chr10:43187175-43187225	AG10803	skin:	n/a
27	chr10:43209934-43209984	HIPEpiC	eye:	n/a
28	chr10:43187184-43187234	SAEC	small airway:	n/a
29	chr10:43186868-43186918	HPAEpiC	pulmonary alveolar:	n/a
30	chr10:43187175-43187225	AoSMC	blood vessel:	n/a
31	chr10:43187175-43187225	NHBE	bronchial:	n/a
32	chr10:43187469-43187519	U87	brain:	n/a
33	chr10:43187175-43187225	CMK	blood:	n/a
34	chr10:43186868-43186918	AoSMC	blood vessel:	n/a
35	chr10:43187321-43187371	IMR90	lung:	fetal
36	chr10:43209934-43209984	BJ	skin:	n/a
37	chr10:43186810-43186860	MCF10A-Er-Src	breast:	n/a
38	chr10:43186900-43186950	K562	blood:	n/a
39	chr10:43187321-43187371	Caco-2	colon:	n/a
40	chr10:43187321-43187371	HNPCEpiC	eye:	n/a
41	chr10:43187321-43187371	SK-N-SH_RA	brain:	n/a
42	chr10:43186868-43186918	HNPCEpiC	eye:	n/a
43	chr10:43187469-43187519	PANC-1	pancreas:	n/a
44	chr10:43186810-43186860	BE2_C	brain:	n/a
45	chr10:43187184-43187234	HRE	kidney:	n/a
46	chr10:43187175-43187225	SK-N-SH_RA	brain:	n/a
47	chr10:43186810-43186860	SKMC	muscle:	n/a
48	chr10:43186868-43186918	Hepatocyte	liver:	n/a
49	chr10:43186900-43186950	Caco-2	colon:	n/a
50	chr10:43209934-43209984	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43179370..43182447-chr10:43184174..43186310,3	MCF-7	breast:
2	chr10:43132797..43134330-chr10:43167529..43170450,2	K562	blood:
3	chr10:43203133..43206798-chr10:43276930..43278950,3	MCF-7	breast:
4	chr10:43132101..43134395-chr10:43180123..43182624,3	K562	blood:
5	chr10:43132526..43135261-chr10:43184647..43186574,3	MCF-7	breast:
6	chr10:43132391..43135100-chr10:43189606..43191108,2	MCF-7	breast:
7	chr10:43173150..43176514-chr10:43178445..43181832,3	K562	blood:
8	chr10:43173150..43176514-chr10:43178445..43181832,3	K562	blood:
9	chr10:43179370..43182447-chr10:43184174..43186310,3	MCF-7	breast:
10	chr10:43132462..43134955-chr10:43172627..43174472,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-1	chr10:43178806-43178908	ENSG00000233515
2	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT139966
3	lnc-ZNF33B-1	chr10:43186181-43186249	NONHSAT139966
4	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT139966
5	lnc-ZNF33B-1	chr10:43169877-43169974	NONHSAT012924
6	lnc-ZNF33B-1	chr10:43169645-43169805	ENSG00000233515
7	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT012921
8	lnc-ZNF33B-1	chr10:43186983-43187198	NONHSAT012921
9	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012921
10	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012921
11	lnc-BMS1-2	chr10:43196950-43197705	ENSG00000234864
12	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT139966
13	lnc-BMS1-2	chr10:43198870-43201901	ENSG00000234864
14	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012924
15	lnc-ZNF33B-1	chr10:43186983-43187171	ENSG00000233515
16	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT012922
17	lnc-BMS1-2	chr10:43191483-43191659	ENSG00000234864
18	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012922
19	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012922
20	lnc-ZNF33B-1	chr10:43187438-43187527	NONHSAT012924
21	lnc-ZNF33B-1	chr10:43181399-43181464	ENSG00000233515
22	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012924
23	lnc-ZNF33B-1	chr10:43186987-43187198	NONHSAT012922

Variant related genes	Relation type
ENSG00000234864	TF binding region
ENSG00000233515	TF binding region
CUBNP1	TF binding region
ENSG00000234864	CpG island
ENSG00000233515	CpG island
CUBNP1	CpG island
ENSG00000196693	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000272373	chromatin interactions

Extended variants
information (count: 1779 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1779 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543572518	chr10:43167536-43167537	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559189270	chr10:43167539-43167540	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186818991	chr10:43167582-43167583	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191630185	chr10:43167584-43167585	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544813024	chr10:43167619-43167620	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs117806265	chr10:43167642-43167643	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533302530	chr10:43167645-43167646	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs140093096	chr10:43167654-43167655	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs184105358	chr10:43167667-43167668	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530836976	chr10:43167677-43167678	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143944703	chr10:43167678-43167679	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373458108	chr10:43167686-43167687	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567760468	chr10:43167722-43167723	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528633162	chr10:43167726-43167727	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188845148	chr10:43167735-43167736	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571838227	chr10:43167739-43167740	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs147338591	chr10:43167743-43167744	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561472560	chr10:43167845-43167846	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530133872	chr10:43167847-43167848	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141012137	chr10:43167933-43167934	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569640694	chr10:43167936-43167937	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550376244	chr10:43167948-43167949	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142079634	chr10:43167951-43167952	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150713037	chr10:43167954-43167955	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114348744	chr10:43167956-43167957	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375195153	chr10:43168018-43168019	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181535725	chr10:43168023-43168024	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113755700	chr10:43168024-43168025	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149908598	chr10:43168056-43168057	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544928795	chr10:43168058-43168059	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73251014	chr10:43168080-43168081	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs532716898	chr10:43168111-43168112	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530776488	chr10:43168142-43168143	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs542617274	chr10:43168176-43168177	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs146441196	chr10:43168211-43168212	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528626846	chr10:43168237-43168238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546863610	chr10:43168239-43168240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571839655	chr10:43168247-43168248	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552924064	chr10:43168296-43168297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532777126	chr10:43168304-43168305	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7097407	chr10:43168350-43168351	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185353607	chr10:43168367-43168368	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs536997743	chr10:43168490-43168491	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190232224	chr10:43168501-43168502	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs567237970	chr10:43168515-43168516	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560755525	chr10:43168538-43168539	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368799573	chr10:43168546-43168547	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2297693	chr10:43168582-43168583	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534608693	chr10:43168645-43168646	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552868327	chr10:43168662-43168663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43168000-43168200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:43168200-43172600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:43169200-43170400	Enhancers	K562	blood
4	chr10:43170400-43175800	Weak transcription	K562	blood
5	chr10:43175800-43176200	Enhancers	K562	blood
6	chr10:43176200-43183000	Weak transcription	K562	blood
7	chr10:43180400-43180800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr10:43182800-43184200	Enhancers	Stomach Mucosa	stomach
9	chr10:43183000-43183200	Enhancers	K562	blood
10	chr10:43183200-43183800	Weak transcription	K562	blood
11	chr10:43183800-43184000	Enhancers	K562	blood
12	chr10:43183800-43184200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr10:43184000-43185200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr10:43184400-43185000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr10:43184400-43185600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:43184600-43185400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:43184600-43185600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr10:43184600-43185600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr10:43185600-43186200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr10:43185600-43186600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:43185800-43186200	Enhancers	Pancreas	Pancrea
22	chr10:43186200-43190400	Weak transcription	Pancreas	Pancrea
23	chr10:43186600-43187000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr10:43187000-43187200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:43187200-43187400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:43187400-43188800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr10:43190000-43191600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:43190200-43191400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:43190600-43191200	Enhancers	HepG2	liver
30	chr10:43190800-43191200	Enhancers	Liver	Liver
31	chr10:43190800-43191600	Enhancers	K562	blood
32	chr10:43191400-43193400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr10:43191600-43193000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:43193000-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:43193400-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:43193600-43194000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr10:43194000-43194400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:43194200-43194600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr10:43202600-43202800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr10:43202800-43203600	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr10:43212600-43213000	Enhancers	Spleen	Spleen
42	chr10:43212800-43213000	Enhancers	HepG2	liver
43	chr10:43213000-43215800	Weak transcription	Spleen	Spleen

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