Variant report

Variant	nsv589860
Chromosome Location	chr3:20419583-20501403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
3	CCNT2	chr3:20500973-20501023	K562	blood:	n/a	n/a
4	CEBPB	chr3:20442866-20443121	HepG2	liver:	n/a	chr3:20442974-20442985
5	CEBPB	chr3:20439795-20440063	K562	blood:	n/a	n/a
6	CEBPB	chr3:20447358-20447747	HepG2	liver:	n/a	chr3:20447481-20447492
7	CEBPB	chr3:20439832-20440032	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:20421835-20421992	K562	blood:	n/a	n/a
9	CEBPB	chr3:20439770-20440049	A549	lung:	n/a	n/a
10	CEBPB	chr3:20421949-20421971	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:20439757-20440083	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:20439732-20440080	HepG2	liver:	n/a	n/a
13	CTCF	chr3:20425961-20426058	Spleen_OC	spleen:	n/a	n/a
14	CTCF	chr3:20440798-20440832	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chr3:20473944-20474006	GM20000	blood:	n/a	n/a
16	CTCF	chr3:20423900-20424050	GM12866	blood:	n/a	n/a
17	CTCF	chr3:20485260-20485324	GM10266	blood:	n/a	n/a
18	CTCF	chr3:20468507-20468543	Lung_OC	lung:	n/a	n/a
19	CTCF	chr3:20421429-20421486	GM13976	blood:	n/a	n/a
20	CTCF	chr3:20476860-20477010	GM12869	blood:	n/a	n/a
21	CTCF	chr3:20448200-20448350	GM12871	blood:	n/a	n/a
22	CUX1	chr3:20419922-20420115	K562	blood:	n/a	n/a
23	E2F4	chr3:20447363-20447582	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr3:20478080-20478220	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr3:20496696-20496745	MCF10A-Er-Src	breast:	n/a	n/a
26	EP300	chr3:20463825-20464440	T-47D	breast:	n/a	n/a
27	EP300	chr3:20500898-20501156	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr3:20500889-20501208	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr3:20463827-20464309	T-47D	breast:	n/a	n/a
30	EP300	chr3:20464757-20464762	K562	blood:	n/a	n/a
31	EP300	chr3:20424412-20424469	GM12878	blood:	n/a	n/a
32	EP300	chr3:20500940-20501145	K562	blood:	n/a	n/a
33	FOS	chr3:20447261-20447639	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr3:20447238-20447631	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr3:20427130-20427287	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:20461130-20461235	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
37	FOS	chr3:20477790-20477990	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:20461170-20461267	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
39	FOS	chr3:20442889-20443042	MCF10A-Er-Src	breast:	n/a	chr3:20443032-20443041
40	FOS	chr3:20477810-20478010	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:20447997-20448170	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:20447289-20447627	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:20461137-20461236	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
44	FOS	chr3:20447258-20447674	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:20488402-20488562	MCF10A-Er-Src	breast:	n/a	n/a
46	FOXA1	chr3:20463817-20464382	T-47D	breast:	n/a	n/a
47	FOXA1	chr3:20463848-20464374	T-47D	breast:	n/a	n/a
48	FOXA1	chr3:20435940-20436185	ECC-1	luminal epithelium:	n/a	n/a
49	FOXA2	chr3:20474218-20474575	A549	lung:	n/a	n/a
50	GATA2	chr3:20500910-20501219	SH-SY5Y	brain:	n/a	chr3:20500991-20501012 chr3:20501103-20501116

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20448283-20448333	NH-A	brain:	n/a
2	chr3:20448283-20448333	CMK	blood:	n/a
3	chr3:20448283-20448333	ProgFib	skin:	n/a
4	chr3:20448283-20448333	SAEC	small airway:	n/a
5	chr3:20448283-20448333	GM12878	blood:	n/a
6	chr3:20448283-20448333	GM19239	blood:	n/a
7	chr3:20448283-20448333	H1-hESC	embryonic stem cell:	embryo
8	chr3:20448283-20448333	K562	blood:	n/a
9	chr3:20448283-20448333	HUVEC	blood vessel:	n/a
10	chr3:20448283-20448333	HRCEpiC	kidney:	n/a
11	chr3:20448283-20448333	T-47D	breast:	n/a
12	chr3:20448283-20448333	ovcar-3	ovarian:	n/a
13	chr3:20448283-20448333	SKMC	muscle:	n/a
14	chr3:20448283-20448333	Jurkat	blood:	n/a
15	chr3:20448283-20448333	U87	brain:	n/a
16	chr3:20448283-20448333	HCT-116	colon:	n/a
17	chr3:20448283-20448333	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:20448283-20448333	RPTEC	kidney:	n/a
19	chr3:20448283-20448333	HEEpiC	esophagus:	n/a
20	chr3:20448283-20448333	HEK293	kidney:	embryo
21	chr3:20448283-20448333	NHDF-neo	bronchial:	n/a
22	chr3:20448283-20448333	NB4	blood:	n/a
23	chr3:20448283-20448333	HAEpiC	amniotic membrane:	n/a
24	chr3:20448283-20448333	GM06990	blood:	n/a
25	chr3:20448283-20448333	A549	lung:	n/a
26	chr3:20448283-20448333	AG04450	lung:	fetal
27	chr3:20448283-20448333	HCM	heart:	n/a
28	chr3:20448283-20448333	IMR90	lung:	fetal
29	chr3:20448283-20448333	NHBE	bronchial:	n/a
30	chr3:20448283-20448333	SK-N-MC	brain:	n/a
31	chr3:20448283-20448333	HRPEpiC	eye:	n/a
32	chr3:20448283-20448333	SK-N-SH	brain:	n/a
33	chr3:20448283-20448333	GM12892	blood:	n/a
34	chr3:20448283-20448333	AG10803	skin:	n/a
35	chr3:20448283-20448333	BJ	skin:	n/a
36	chr3:20448283-20448333	NT2-D1	testis:	n/a
37	chr3:20448283-20448333	GM12891	blood:	n/a
38	chr3:20448283-20448333	HCF	heart:	n/a
39	chr3:20448283-20448333	Hela-S3	cervix:	n/a
40	chr3:20448283-20448333	HCPEpiC	choroid plexus:	n/a
41	chr3:20448283-20448333	Caco-2	colon:	n/a
42	chr3:20448283-20448333	HL-60	blood:	n/a
43	chr3:20448283-20448333	HRE	kidney:	n/a
44	chr3:20448283-20448333	AoSMC	blood vessel:	n/a
45	chr3:20448283-20448333	Hepatocyte	liver:	n/a
46	chr3:20448283-20448333	SK-N-SH_RA	brain:	n/a
47	chr3:20448283-20448333	MCF10A-Er-Src	breast:	n/a
48	chr3:20448283-20448333	MCF-7	breast:	n/a
49	chr3:20448283-20448333	AG09309	skin:	n/a
50	chr3:20448283-20448333	HIPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
2	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
3	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
4	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
5	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
6	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
7	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
8	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
ENSG00000261734	CpG island

Extended variants
information (count: 1861 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1861 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6768597	chr3:20419583-20419584	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78899767	chr3:20419590-20419591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534203860	chr3:20419608-20419609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367688151	chr3:20419647-20419648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556028828	chr3:20419649-20419650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs80013051	chr3:20419740-20419741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535589693	chr3:20419754-20419755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192581888	chr3:20419755-20419756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575150382	chr3:20419780-20419781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182612384	chr3:20419811-20419812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563907140	chr3:20419854-20419855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376064677	chr3:20419861-20419862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370268532	chr3:20419863-20419864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573127878	chr3:20419869-20419870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187619035	chr3:20419912-20419913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77809179	chr3:20420008-20420009	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529008579	chr3:20420030-20420031	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192891284	chr3:20420039-20420040	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570191554	chr3:20420061-20420062	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141252035	chr3:20420106-20420107	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562608759	chr3:20420112-20420113	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539211287	chr3:20420145-20420146	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144552882	chr3:20420253-20420254	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115949497	chr3:20420273-20420274	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566736541	chr3:20420305-20420306	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184951757	chr3:20420373-20420374	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549692966	chr3:20420408-20420409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75243580	chr3:20420435-20420436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538397851	chr3:20420504-20420505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188845082	chr3:20420507-20420508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575329029	chr3:20420516-20420517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191953945	chr3:20420566-20420567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559164131	chr3:20420622-20420623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557776441	chr3:20420659-20420660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572749088	chr3:20420691-20420692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62241798	chr3:20420704-20420705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577826967	chr3:20420790-20420791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139267216	chr3:20420791-20420792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184421247	chr3:20420792-20420793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375422300	chr3:20420828-20420829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573516999	chr3:20420834-20420835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543974728	chr3:20420848-20420849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189151784	chr3:20420861-20420862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553490319	chr3:20420871-20420872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545161601	chr3:20420879-20420880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144053221	chr3:20420905-20420906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527636024	chr3:20420908-20420909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549705210	chr3:20420915-20420916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145961925	chr3:20420917-20420918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573578302	chr3:20420972-20420973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20417000-20420000	Enhancers	Fetal Intestine Large	intestine
2	chr3:20418200-20420200	Enhancers	Fetal Intestine Small	intestine
3	chr3:20418400-20419600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr3:20418400-20420000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:20418400-20420000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:20418400-20420400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:20418600-20420200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:20418600-20420200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:20419000-20419800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr3:20419200-20419800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:20419200-20420400	Enhancers	Duodenum Mucosa	Duodenum
12	chr3:20419400-20420000	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr3:20419800-20420000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:20419800-20420200	Enhancers	Fetal Stomach	stomach
15	chr3:20419800-20420600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:20420000-20420200	Enhancers	Small Intestine	intestine
17	chr3:20420000-20420400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:20420000-20421800	Weak transcription	Fetal Intestine Large	intestine
19	chr3:20420200-20421800	Weak transcription	Fetal Intestine Small	intestine
20	chr3:20420400-20421800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:20421800-20422000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:20421800-20422200	Enhancers	Aorta	Aorta
23	chr3:20421800-20422200	Enhancers	Fetal Intestine Large	intestine
24	chr3:20421800-20422200	Enhancers	Fetal Intestine Small	intestine
25	chr3:20422000-20422200	Enhancers	Fetal Stomach	stomach
26	chr3:20422200-20423400	Weak transcription	Fetal Intestine Large	intestine
27	chr3:20422200-20423400	Weak transcription	Fetal Intestine Small	intestine
28	chr3:20423400-20424800	Enhancers	Fetal Intestine Large	intestine
29	chr3:20423400-20425000	Enhancers	Fetal Intestine Small	intestine
30	chr3:20426800-20427600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
31	chr3:20427600-20433200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr3:20433000-20433400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:20433000-20433600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr3:20433200-20433400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr3:20433200-20433600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:20433400-20435800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr3:20433600-20435800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr3:20435600-20436200	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr3:20435800-20436000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr3:20435800-20436200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr3:20435800-20436200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:20435800-20436200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:20435800-20436200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:20436000-20436200	ZNF genes & repeats	Pancreas	Pancrea
45	chr3:20436000-20448200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:20436200-20445200	Weak transcription	Fetal Intestine Small	intestine
47	chr3:20436200-20445800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:20436200-20453400	Weak transcription	Pancreas	Pancrea
49	chr3:20437800-20438400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr3:20441400-20442000	Enhancers	Aorta	Aorta

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