Variant report

Variant	esv3342274
Chromosome Location	chr10:5875995-5901345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:695)
CpG islands
(count:552)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5888296-5888348	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5895391-5895857	K562	blood:	n/a	n/a
3	ARID3A	chr10:5887078-5887316	K562	blood:	n/a	n/a
4	ARID3A	chr10:5882378-5882749	HepG2	liver:	n/a	n/a
5	ATF2	chr10:5895386-5895843	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:5887991-5888533	GM12878	blood:	n/a	n/a
7	ATF2	chr10:5885726-5886294	GM12878	blood:	n/a	n/a
8	ATF2	chr10:5888079-5888517	GM12878	blood:	n/a	n/a
9	ATF2	chr10:5882081-5882634	GM12878	blood:	n/a	n/a
10	ATF2	chr10:5882822-5883381	GM12878	blood:	n/a	n/a
11	ATF2	chr10:5894153-5894810	GM12878	blood:	n/a	n/a
12	ATF2	chr10:5894122-5894884	GM12878	blood:	n/a	n/a
13	ATF2	chr10:5885759-5886344	GM12878	blood:	n/a	n/a
14	ATF2	chr10:5882088-5883394	GM12878	blood:	n/a	n/a
15	ATF3	chr10:5895229-5895945	HCT-116	colon:	n/a	n/a
16	ATF3	chr10:5895226-5895940	K562	blood:	n/a	n/a
17	ATF3	chr10:5895238-5896003	HCT-116	colon:	n/a	n/a
18	ATF3	chr10:5887049-5887248	K562	blood:	n/a	chr10:5887191-5887200 chr10:5887191-5887211
19	ATF3	chr10:5895150-5896042	A549	lung:	n/a	n/a
20	ATF3	chr10:5895143-5896014	A549	lung:	n/a	n/a
21	BACH1	chr10:5883022-5883034	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr10:5894178-5894732	GM12878	blood:	n/a	n/a
23	BATF	chr10:5895558-5895813	GM12878	blood:	n/a	n/a
24	BATF	chr10:5882191-5882590	GM12878	blood:	n/a	chr10:5882324-5882334
25	BATF	chr10:5888145-5888416	GM12878	blood:	n/a	n/a
26	BATF	chr10:5888064-5888456	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:5882223-5882654	GM12878	blood:	n/a	n/a
28	BCL11A	chr10:5885938-5886268	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:5894373-5894676	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:5888140-5888401	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:5882236-5882572	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:5888070-5888508	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:5882963-5883335	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:5894328-5894755	GM12878	blood:	n/a	n/a
35	BCL3	chr10:5897974-5898199	GM12878	blood:	n/a	n/a
36	BCL3	chr10:5882190-5882621	GM12878	blood:	n/a	n/a
37	BCL3	chr10:5897892-5898308	GM12878	blood:	n/a	n/a
38	BCL3	chr10:5894308-5894826	GM12878	blood:	n/a	n/a
39	BCL3	chr10:5888086-5888466	GM12878	blood:	n/a	n/a
40	BCLAF1	chr10:5894146-5894742	GM12878	blood:	n/a	n/a
41	BCLAF1	chr10:5888041-5888445	GM12878	blood:	n/a	n/a
42	BCLAF1	chr10:5895360-5895838	K562	blood:	n/a	n/a
43	BCLAF1	chr10:5882114-5882863	GM12878	blood:	n/a	n/a
44	BCLAF1	chr10:5895284-5895831	GM12878	blood:	n/a	n/a
45	BCLAF1	chr10:5894072-5894846	GM12878	blood:	n/a	n/a
46	BCLAF1	chr10:5885619-5886233	GM12878	blood:	n/a	n/a
47	BCLAF1	chr10:5882182-5883297	GM12878	blood:	n/a	n/a
48	BCLAF1	chr10:5886650-5887130	GM12878	blood:	n/a	n/a
49	BCLAF1	chr10:5895230-5895756	GM12878	blood:	n/a	n/a
50	BDP1	chr10:5895563-5895963	K562	blood:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5886111-5886161	BE2_C	brain:	n/a
2	chr10:5884153-5884203	GM12891	blood:	n/a
3	chr10:5884105-5884155	Caco-2	colon:	n/a
4	chr10:5886111-5886161	BE2_C	brain:	n/a
5	chr10:5884153-5884203	GM12891	blood:	n/a
6	chr10:5884105-5884155	Caco-2	colon:	n/a
7	chr10:5882304-5882354	NB4	blood:	n/a
8	chr10:5879090-5879140	HPAEpiC	pulmonary alveolar:	n/a
9	chr10:5884153-5884203	SK-N-MC	brain:	n/a
10	chr10:5882576-5882626	PFSK-1	brain:	n/a
11	chr10:5886111-5886161	HIPEpiC	eye:	n/a
12	chr10:5882304-5882354	AoSMC	blood vessel:	n/a
13	chr10:5882466-5882516	GM12891	blood:	n/a
14	chr10:5879090-5879140	GM12878	blood:	n/a
15	chr10:5882304-5882354	ECC-1	luminal epithelium:	n/a
16	chr10:5882739-5882789	HL-60	blood:	n/a
17	chr10:5879090-5879140	SK-N-SH_RA	brain:	n/a
18	chr10:5884105-5884155	AG04449	skin:	fetal
19	chr10:5879090-5879140	NHDF-neo	bronchial:	n/a
20	chr10:5886111-5886161	NB4	blood:	n/a
21	chr10:5882304-5882354	NHBE	bronchial:	n/a
22	chr10:5884105-5884155	AG10803	skin:	n/a
23	chr10:5884105-5884155	SKMC	muscle:	n/a
24	chr10:5884061-5884111	HCF	heart:	n/a
25	chr10:5884105-5884155	HCT-116	colon:	n/a
26	chr10:5882739-5882789	ovcar-3	ovarian:	n/a
27	chr10:5882739-5882789	PANC-1	pancreas:	n/a
28	chr10:5884105-5884155	CMK	blood:	n/a
29	chr10:5882466-5882516	HEK293	kidney:	embryo
30	chr10:5882576-5882626	SK-N-SH	brain:	n/a
31	chr10:5882304-5882354	HRE	kidney:	n/a
32	chr10:5882576-5882626	GM12892	blood:	n/a
33	chr10:5882304-5882354	HCT-116	colon:	n/a
34	chr10:5879090-5879140	HCM	heart:	n/a
35	chr10:5884153-5884203	SK-N-SH_RA	brain:	n/a
36	chr10:5884105-5884155	HUVEC	blood vessel:	n/a
37	chr10:5882466-5882516	GM19239	blood:	n/a
38	chr10:5884061-5884111	NT2-D1	testis:	n/a
39	chr10:5884061-5884111	Hela-S3	cervix:	n/a
40	chr10:5882466-5882516	SAEC	small airway:	n/a
41	chr10:5884105-5884155	PrEC	prostate:	n/a
42	chr10:5882739-5882789	GM19239	blood:	n/a
43	chr10:5886111-5886161	MCF-7	breast:	n/a
44	chr10:5886111-5886161	NHDF-neo	bronchial:	n/a
45	chr10:5884061-5884111	SK-N-SH_RA	brain:	n/a
46	chr10:5886111-5886161	SAEC	small airway:	n/a
47	chr10:5882466-5882516	ovcar-3	ovarian:	n/a
48	chr10:5879090-5879140	GM19239	blood:	n/a
49	chr10:5882466-5882516	U87	brain:	n/a
50	chr10:5882576-5882626	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:5854140..5856929-chr10:5898558..5900231,2	MCF-7	breast:
2	chr10:5868411..5871104-chr10:5884225..5887747,3	K562	blood:
3	chr10:5876253..5877969-chr10:5881683..5883648,2	K562	blood:
4	chr10:5853523..5857550-chr10:5895504..5898472,4	K562	blood:
5	chr10:5850597..5856224-chr10:5899689..5902412,5	K562	blood:
6	chr10:5854620..5857118-chr10:5886149..5888419,4	K562	blood:
7	chr10:5874603..5876795-chr10:5886014..5887751,3	MCF-7	breast:
8	chr10:5874179..5876350-chr10:5894206..5896113,2	K562	blood:
9	chr10:5853712..5856413-chr10:5877125..5879138,3	MCF-7	breast:
10	chr10:5887234..5889271-chr10:5891738..5894895,3	K562	blood:
11	chr10:5870260..5872899-chr10:5873504..5877637,4	K562	blood:
12	chr10:5876253..5877969-chr10:5881683..5883648,2	K562	blood:
13	chr10:5874889..5877951-chr10:5883018..5886610,3	MCF-7	breast:
14	chr10:5887234..5889271-chr10:5891738..5894895,3	K562	blood:
15	chr10:5871204..5872899-chr10:5874747..5877637,3	K562	blood:
16	chr10:5835385..5837024-chr10:5893151..5895747,2	MCF-7	breast:
17	chr10:5887749..5890618-chr10:5895657..5897180,2	K562	blood:
18	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
19	chr10:5850597..5853484-chr10:5898526..5901196,3	K562	blood:
20	chr10:5853185..5855023-chr10:5896110..5898472,2	K562	blood:
21	chr10:5853267..5855548-chr10:5881785..5884894,3	MCF-7	breast:
22	chr10:5875866..5877647-chr10:5881023..5883616,2	K562	blood:
23	chr10:5860095..5862542-chr10:5886681..5888594,2	MCF-7	breast:
24	chr10:5886207..5890565-chr10:5893992..5897304,3	K562	blood:
25	chr10:5874603..5876795-chr10:5886014..5887751,3	MCF-7	breast:
26	chr10:5886207..5890565-chr10:5893992..5897304,3	K562	blood:
27	chr10:5852230..5858723-chr10:5874443..5879399,10	K562	blood:
28	chr10:5853739..5856663-chr10:5888964..5891448,2	MCF-7	breast:
29	chr10:5872995..5874657-chr10:5893099..5894735,2	K562	blood:
30	chr10:5852473..5857853-chr10:5880942..5888645,8	MCF-7	breast:
31	chr10:5874179..5876350-chr10:5894206..5896113,2	K562	blood:
32	chr10:5853822..5855522-chr10:5894959..5897047,2	MCF-7	breast:
33	chr10:5850869..5856128-chr10:5879241..5885807,8	K562	blood:
34	chr10:5900731..5902492-chr10:5915568..5917160,2	K562	blood:
35	chr10:5875866..5877647-chr10:5881023..5883616,2	K562	blood:
36	chr10:5887749..5890618-chr10:5895657..5897180,2	K562	blood:
37	chr10:5851448..5853265-chr10:5875008..5877610,2	MCF-7	breast:
38	chr10:5854377..5856986-chr10:5893024..5895477,2	MCF-7	breast:
39	chr10:5851570..5858995-chr10:5881654..5887342,9	K562	blood:
40	chr10:5889255..5891417-chr10:5903224..5906135,2	MCF-7	breast:
41	chr10:5854265..5856578-chr10:5874847..5876421,2	MCF-7	breast:
42	chr10:5857495..5859789-chr10:5881654..5883847,2	K562	blood:
43	chr10:5855459..5857550-chr10:5896557..5898407,2	K562	blood:

No data

Variant related genes	Relation type
GDI2	TF binding region
GDI2	CpG island
ENSG00000240180	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 1084 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1084 , 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	rs116217312	chr10:5876023-5876024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558912998	chr10:5876063-5876064	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs72774112	chr10:5876177-5876178	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs186244116	chr10:5876184-5876185	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs572680232	chr10:5876207-5876208	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115157695	chr10:5876228-5876229	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs117602649	chr10:5876304-5876305	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs542886600	chr10:5876356-5876357	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188137693	chr10:5876357-5876358	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141236272	chr10:5876358-5876359	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138661985	chr10:5876377-5876378	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543024851	chr10:5876416-5876417	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564913000	chr10:5876431-5876432	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138709800	chr10:5876457-5876458	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs180675682	chr10:5876458-5876459	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541306813	chr10:5876469-5876470	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs559996426	chr10:5876545-5876546	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs117742823	chr10:5876556-5876557	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs56235546	chr10:5876606-5876607	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
20	rs560823048	chr10:5876610-5876611	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531530949	chr10:5876628-5876629	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs540953972	chr10:5876633-5876634	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs11255472	chr10:5876643-5876644	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs185495500	chr10:5876673-5876674	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114009889	chr10:5876749-5876750	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145141724	chr10:5876753-5876754	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549698252	chr10:5876792-5876793	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535044730	chr10:5876813-5876814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs61832880	chr10:5876823-5876824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs61832881	chr10:5876833-5876834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs61832882	chr10:5876839-5876840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554103096	chr10:5876856-5876857	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs61832893	chr10:5876857-5876858	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs61832894	chr10:5876867-5876868	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs61832895	chr10:5876870-5876871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61832896	chr10:5876875-5876876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs61832897	chr10:5876879-5876880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs61832898	chr10:5876882-5876883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs61832899	chr10:5876891-5876892	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs61832900	chr10:5876899-5876900	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11255474	chr10:5876945-5876946	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs536408627	chr10:5876952-5876953	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529286396	chr10:5876966-5876967	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554773291	chr10:5877018-5877019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576022898	chr10:5877027-5877028	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140549510	chr10:5877129-5877130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543491883	chr10:5877193-5877194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12220359	chr10:5877213-5877214	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
49	rs75844011	chr10:5877229-5877230	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540666165	chr10:5877237-5877238	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5873200-5882400	Weak transcription	Spleen	Spleen
2	chr10:5874600-5876400	Enhancers	Placenta	Placenta
3	chr10:5874800-5876000	Enhancers	Fetal Heart	heart
4	chr10:5875000-5876000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:5875000-5886600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr10:5875200-5877600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:5875200-5882200	Weak transcription	Right Atrium	heart
8	chr10:5875400-5876000	Weak transcription	Left Ventricle	heart
9	chr10:5875400-5876200	Weak transcription	Gastric	stomach
10	chr10:5875600-5876000	Flanking Active TSS	K562	blood
11	chr10:5875600-5876200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr10:5875800-5876000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:5875800-5876000	Enhancers	Stomach Mucosa	stomach
14	chr10:5875800-5876000	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr10:5875800-5876600	Enhancers	Fetal Muscle Leg	muscle
16	chr10:5875800-5876600	Enhancers	Right Ventricle	heart
17	chr10:5876000-5876400	Flanking Active TSS	Fetal Heart	heart
18	chr10:5876000-5876600	Enhancers	Left Ventricle	heart
19	chr10:5876000-5876800	Bivalent Enhancer	HepG2	liver
20	chr10:5876000-5878000	Enhancers	K562	blood
21	chr10:5876200-5876600	Enhancers	Gastric	stomach
22	chr10:5876200-5882200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr10:5876400-5876800	Enhancers	Fetal Heart	heart
24	chr10:5876400-5876800	Weak transcription	Placenta	Placenta
25	chr10:5876600-5882600	Weak transcription	Left Ventricle	heart
26	chr10:5876800-5878600	Enhancers	Placenta	Placenta
27	chr10:5877200-5877400	Bivalent Enhancer	HepG2	liver
28	chr10:5877400-5877600	Enhancers	HepG2	liver
29	chr10:5877600-5877800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:5877600-5878200	Flanking Active TSS	HepG2	liver
31	chr10:5877800-5882400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:5878000-5885600	Weak transcription	K562	blood
33	chr10:5878200-5878400	Enhancers	HepG2	liver
34	chr10:5878200-5881800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr10:5878600-5881600	Weak transcription	Placenta	Placenta
36	chr10:5880000-5882200	Enhancers	Primary B cells from peripheral blood	blood
37	chr10:5880000-5882400	Enhancers	Primary B cells from cord blood	blood
38	chr10:5881000-5881200	Enhancers	NHLF	lung
39	chr10:5881000-5882200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr10:5881200-5882000	Weak transcription	NHLF	lung
41	chr10:5881400-5882400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr10:5881600-5882200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr10:5881600-5882200	Active TSS	Brain Angular Gyrus	brain
44	chr10:5881600-5882200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr10:5881600-5882200	Enhancers	GM12878-XiMat	blood
46	chr10:5881600-5882400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr10:5881600-5882600	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr10:5881600-5882800	Enhancers	NHDF-Ad	bronchial
49	chr10:5881600-5883000	Enhancers	Placenta	Placenta
50	chr10:5881600-5883200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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