Variant report

Variant	nsv1057629
Chromosome Location	chr18:44500259-44539223
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	chr18:44530288-44530439	K562	blood:	n/a	n/a
2	BRCA1	chr18:44526800-44527412	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr18:44519517-44519902	HCT-116	colon:	n/a	n/a
4	CEBPB	chr18:44533294-44533502	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr18:44519633-44519970	IMR90	lung:	n/a	n/a
6	CEBPB	chr18:44517540-44517817	IMR90	lung:	n/a	chr18:44517683-44517694
7	CEBPB	chr18:44517542-44517844	HepG2	liver:	n/a	chr18:44517683-44517694
8	CEBPB	chr18:44519678-44519944	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr18:44519588-44519974	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr18:44517559-44517759	K562	blood:	n/a	chr18:44517683-44517694
11	CHD2	chr18:44526653-44526788	K562	blood:	n/a	n/a
12	CHD2	chr18:44526479-44527130	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:44530103-44530335	K562	blood:	n/a	chr18:44530204-44530222
14	CTCF	chr18:44530140-44530290	GM12870	blood:	n/a	chr18:44530204-44530222
15	CTCF	chr18:44530140-44530290	GM12873	blood:	n/a	chr18:44530204-44530222
16	CTCF	chr18:44530160-44530310	HRE	kidney:	n/a	chr18:44530204-44530222
17	CTCF	chr18:44530238-44530323	NHEK	skin:	n/a	n/a
18	CTCF	chr18:44530137-44530348	Gliobla	brain:	n/a	chr18:44530204-44530222
19	CTCF	chr18:44530160-44530310	GM12869	blood:	n/a	chr18:44530204-44530222
20	CTCF	chr18:44530140-44530290	GM12865	blood:	n/a	chr18:44530204-44530222
21	CTCF	chr18:44530203-44530338	Fibrobl	skin:	n/a	chr18:44530204-44530222
22	CTCF	chr18:44529500-44529650	BJ	skin:	n/a	n/a
23	CTCF	chr18:44530140-44530290	WERI-Rb-1	eye:	n/a	chr18:44530204-44530222
24	CTCF	chr18:44530076-44530273	A549	lung:	n/a	chr18:44530204-44530222
25	CTCF	chr18:44529880-44530030	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr18:44530100-44530250	GM12871	blood:	n/a	chr18:44530204-44530222
27	CTCF	chr18:44530100-44530250	HFF-Myc	foreskin:	n/a	chr18:44530204-44530222
28	CTCF	chr18:44529800-44529950	GM12878	blood:	n/a	n/a
29	CTCF	chr18:44529820-44529970	HEK293	kidney:	n/a	n/a
30	CTCF	chr18:44530090-44530358	HUVEC	blood vessel:	n/a	chr18:44530204-44530222
31	CTCF	chr18:44529995-44530386	H1-hESC	embryonic stem cell:	n/a	chr18:44530204-44530222
32	CTCF	chr18:44530120-44530270	Hela-S3	cervix:	n/a	chr18:44530204-44530222
33	CTCF	chr18:44529500-44529650	HEK293	kidney:	n/a	n/a
34	CTCF	chr18:44530120-44530270	HRPEpiC	eye:	n/a	chr18:44530204-44530222
35	CTCF	chr18:44530140-44530317	HepG2	liver:	n/a	chr18:44530204-44530222
36	CTCF	chr18:44530046-44530388	IMR90	lung:	n/a	chr18:44530204-44530222
37	CTCF	chr18:44530140-44530290	HEEpiC	esophagus:	n/a	chr18:44530204-44530222
38	CTCF	chr18:44530146-44530315	GM13976	blood:	n/a	chr18:44530204-44530222
39	CTCF	chr18:44530160-44530310	HPF	lung:	n/a	chr18:44530204-44530222
40	CTCF	chr18:44530160-44530310	HPAF	blood vessel:	n/a	chr18:44530204-44530222
41	CTCF	chr18:44530140-44530290	Hela-S3	cervix:	n/a	chr18:44530204-44530222
42	CTCF	chr18:44530160-44530310	MCF-7	breast:	n/a	chr18:44530204-44530222
43	CTCF	chr18:44530200-44530350	HBMEC	blood vessel:	n/a	chr18:44530204-44530222
44	CTCF	chr18:44530100-44530250	HMEC	breast:	n/a	chr18:44530204-44530222
45	CTCF	chr18:44527360-44527510	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr18:44530160-44530310	HA-sp	spinal cord:	n/a	chr18:44530204-44530222
47	CTCF	chr18:44529820-44529970	GM12865	blood:	n/a	n/a
48	CTCF	chr18:44530180-44530330	GM06990	blood:	n/a	chr18:44530204-44530222
49	CTCF	chr18:44530208-44530352	GM19238	blood:	n/a	n/a
50	CTCF	chr18:44530140-44530290	HFF	foreskin:	n/a	chr18:44530204-44530222

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44526605-44526655	A549	lung:	n/a
2	chr18:44526605-44526655	A549	lung:	n/a
3	chr18:44500261-44500311	PrEC	prostate:	n/a
4	chr18:44500261-44500311	SK-N-MC	brain:	n/a
5	chr18:44525710-44525760	SAEC	small airway:	n/a
6	chr18:44530218-44530268	Hela-S3	cervix:	n/a
7	chr18:44526707-44526757	NT2-D1	testis:	n/a
8	chr18:44526430-44526480	SK-N-SH	brain:	n/a
9	chr18:44526700-44526750	BJ	skin:	n/a
10	chr18:44526430-44526480	ECC-1	luminal epithelium:	n/a
11	chr18:44500261-44500311	ovcar-3	ovarian:	n/a
12	chr18:44526430-44526480	HNPCEpiC	eye:	n/a
13	chr18:44526605-44526655	HCM	heart:	n/a
14	chr18:44526430-44526480	CMK	blood:	n/a
15	chr18:44526756-44526806	SAEC	small airway:	n/a
16	chr18:44523070-44523120	HCM	heart:	n/a
17	chr18:44526700-44526750	AG04450	lung:	fetal
18	chr18:44526707-44526757	NHDF-neo	bronchial:	n/a
19	chr18:44525710-44525760	LNCaP	prostate:	n/a
20	chr18:44526743-44526793	ovcar-3	ovarian:	n/a
21	chr18:44527971-44528021	HMEC	breast:	n/a
22	chr18:44526700-44526750	SK-N-SH	brain:	n/a
23	chr18:44525710-44525760	A549	lung:	n/a
24	chr18:44526700-44526750	LNCaP	prostate:	n/a
25	chr18:44526700-44526750	A549	lung:	n/a
26	chr18:44526756-44526806	ovcar-3	ovarian:	n/a
27	chr18:44526743-44526793	BE2_C	brain:	n/a
28	chr18:44526867-44526917	SK-N-SH_RA	brain:	n/a
29	chr18:44526605-44526655	HMEC	breast:	n/a
30	chr18:44527026-44527076	HCM	heart:	n/a
31	chr18:44526743-44526793	Hela-S3	cervix:	n/a
32	chr18:44526707-44526757	Hela-S3	cervix:	n/a
33	chr18:44527026-44527076	PrEC	prostate:	n/a
34	chr18:44527971-44528021	GM19239	blood:	n/a
35	chr18:44530218-44530268	H1-hESC	embryonic stem cell:	embryo
36	chr18:44526700-44526750	SK-N-MC	brain:	n/a
37	chr18:44526867-44526917	HRPEpiC	eye:	n/a
38	chr18:44526743-44526793	Jurkat	blood:	n/a
39	chr18:44526700-44526750	U87	brain:	n/a
40	chr18:44526867-44526917	NHBE	bronchial:	n/a
41	chr18:44526430-44526480	HAEpiC	amniotic membrane:	n/a
42	chr18:44523070-44523120	HIPEpiC	eye:	n/a
43	chr18:44500261-44500311	IMR90	lung:	fetal
44	chr18:44523070-44523120	HRPEpiC	eye:	n/a
45	chr18:44526430-44526480	PFSK-1	brain:	n/a
46	chr18:44526430-44526480	Hela-S3	cervix:	n/a
47	chr18:44527971-44528021	Jurkat	blood:	n/a
48	chr18:44527026-44527076	IMR90	lung:	fetal
49	chr18:44525710-44525760	SK-N-MC	brain:	n/a
50	chr18:44526867-44526917	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44497069..44499203-chr18:44524229..44526403,2	MCF-7	breast:
2	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
3	chr18:44526928..44528966-chr18:44543505..44545090,2	MCF-7	breast:
4	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:
5	chr18:44496509..44498962-chr18:44499238..44501525,3	MCF-7	breast:

Variant related genes	Relation type
PIAS2	TF binding region
KATNAL2	TF binding region
PIAS2	CpG island
KATNAL2	CpG island
ENSG00000266996	chromatin interactions
ENSG00000167216	chromatin interactions
ENSG00000078043	chromatin interactions

Extended variants
information (count: 1066 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532302931	chr18:44500269-44500270	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs368694933	chr18:44500309-44500310	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575822634	chr18:44500360-44500361	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs370286368	chr18:44500382-44500383	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376467957	chr18:44500407-44500408	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs575879415	chr18:44500412-44500413	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs184922962	chr18:44500415-44500416	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs556963499	chr18:44500429-44500430	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs373811474	chr18:44500448-44500449	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs112363277	chr18:44500457-44500458	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs544500607	chr18:44500472-44500473	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs142497339	chr18:44500474-44500475	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs189535343	chr18:44500484-44500485	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs144727482	chr18:44500557-44500558	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs528279917	chr18:44500647-44500648	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541705303	chr18:44500658-44500659	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546182019	chr18:44500705-44500706	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs561993306	chr18:44500706-44500707	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs558367347	chr18:44500725-44500726	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs181087579	chr18:44500754-44500755	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs376529656	chr18:44500793-44500794	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs367978905	chr18:44500795-44500796	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs575079149	chr18:44500826-44500827	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs185878055	chr18:44500943-44500944	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs72917116	chr18:44500951-44500952	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7240909	chr18:44500996-44500997	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs546645859	chr18:44501043-44501044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574758741	chr18:44501044-44501045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191179829	chr18:44501053-44501054	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs7241061	chr18:44501066-44501067	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563010840	chr18:44501113-44501114	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569451193	chr18:44501114-44501115	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs538129428	chr18:44501120-44501121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558493589	chr18:44501121-44501122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147916610	chr18:44501160-44501161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540584142	chr18:44501175-44501176	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140488916	chr18:44501177-44501178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572878570	chr18:44501182-44501183	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs181975562	chr18:44501185-44501186	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561696643	chr18:44501201-44501202	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150409443	chr18:44501217-44501218	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs544053229	chr18:44501220-44501221	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564045506	chr18:44501226-44501227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533155302	chr18:44501231-44501232	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186287679	chr18:44501235-44501236	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560622417	chr18:44501242-44501243	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs529336724	chr18:44501244-44501245	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549478971	chr18:44501264-44501265	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs138126106	chr18:44501266-44501267	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538443605	chr18:44501271-44501272	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44499000-44502800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr18:44500000-44500400	Enhancers	Gastric	stomach
3	chr18:44500000-44500400	Enhancers	Right Atrium	heart
4	chr18:44500200-44500400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr18:44500400-44500800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr18:44500800-44501200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr18:44508400-44509000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr18:44508400-44509200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
9	chr18:44515000-44515400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr18:44515000-44515600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr18:44515000-44515600	Enhancers	HUVEC	blood vessel
12	chr18:44515200-44515400	Enhancers	Colon Smooth Muscle	Colon
13	chr18:44515200-44515600	Enhancers	Adipose Nuclei	Adipose
14	chr18:44515200-44515600	Enhancers	Placenta	Placenta
15	chr18:44515200-44515600	Enhancers	Psoas Muscle	Psoas
16	chr18:44515600-44520800	Weak transcription	Psoas Muscle	Psoas
17	chr18:44518400-44521000	Enhancers	HSMM	muscle
18	chr18:44518800-44519200	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr18:44518800-44519400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr18:44518800-44520000	Enhancers	HSMMtube	muscle
21	chr18:44518800-44520200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr18:44518800-44520400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr18:44518800-44520400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr18:44518800-44520800	Enhancers	NHLF	lung
25	chr18:44519000-44519200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr18:44519000-44520200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr18:44519000-44520200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr18:44519000-44520200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr18:44519000-44520400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr18:44519000-44520800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr18:44519000-44520800	Enhancers	NHDF-Ad	bronchial
32	chr18:44519000-44521000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr18:44519000-44521000	Enhancers	Fetal Muscle Leg	muscle
34	chr18:44519000-44521200	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr18:44519200-44519600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr18:44519200-44520800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr18:44519200-44520800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr18:44519200-44520800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr18:44519400-44519600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:44519400-44519600	Enhancers	Colon Smooth Muscle	Colon
41	chr18:44519400-44519800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr18:44519400-44520000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr18:44519400-44520000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr18:44519400-44520000	Enhancers	HMEC	breast
47	chr18:44519400-44520200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:44519400-44520200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr18:44519400-44520200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr18:44519400-44520200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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