Variant report

Variant	nsv1050609
Chromosome Location	chr10:606328-641404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:1771)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844
2	BHLHE40	chr10:639950-640123	K562	blood:	n/a	chr10:640070-640079 chr10:640064-640085 chr10:640068-640081 chr10:640069-640078
3	CEBPB	chr10:639844-640483	IMR90	lung:	n/a	n/a
4	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
5	CEBPB	chr10:617766-618133	IMR90	lung:	n/a	n/a
6	CEBPB	chr10:640267-640478	A549	lung:	n/a	n/a
7	CTCF	chr10:634162-634412	T-47D	breast:	n/a	n/a
8	CTCF	chr10:634180-634330	HRE	kidney:	n/a	n/a
9	CTCF	chr10:631961-631995	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr10:619302-619504	MCF-7	breast:	n/a	n/a
11	CTCF	chr10:619340-619490	K562	blood:	n/a	n/a
12	CTCF	chr10:631540-631690	Caco-2	colon:	n/a	n/a
13	CTCF	chr10:631920-632070	HepG2	liver:	n/a	n/a
14	CTCF	chr10:619261-619474	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:634160-634310	HPF	lung:	n/a	n/a
16	CTCF	chr10:634090-634346	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:634117-634348	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:631640-631790	BE2_C	brain:	n/a	n/a
19	CTCF	chr10:631474-631937	MCF-7	breast:	n/a	n/a
20	CTCF	chr10:631520-631670	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr10:634172-634318	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr10:619240-619390	HRE	kidney:	n/a	n/a
23	CTCF	chr10:619320-619470	HEK293	kidney:	n/a	n/a
24	CTCF	chr10:632040-632190	HAc	cerebellar:	n/a	n/a
25	CTCF	chr10:615814-615836	GM13976	blood:	n/a	n/a
26	CTCF	chr10:619268-619481	K562	blood:	n/a	n/a
27	CTCF	chr10:634180-634330	AG04450	lung:	n/a	n/a
28	CTCF	chr10:631529-631825	K562	blood:	n/a	n/a
29	CTCF	chr10:634164-634497	MCF-7	breast:	n/a	chr10:634453-634466
30	CTCF	chr10:634121-634337	MCF-7	breast:	n/a	n/a
31	CTCF	chr10:634167-634293	GM12891	blood:	n/a	n/a
32	CTCF	chr10:631580-631730	HPF	lung:	n/a	n/a
33	CTCF	chr10:632002-632008	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr10:634160-634310	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr10:634160-634310	HepG2	liver:	n/a	n/a
36	CTCF	chr10:634177-634275	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr10:617640-617790	GM12871	blood:	n/a	n/a
38	CTCF	chr10:634090-634406	GM12878	blood:	n/a	n/a
39	CTCF	chr10:634160-634310	HVMF	connective:	n/a	n/a
40	CTCF	chr10:619305-619505	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:631504-631776	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:634220-634370	RPTEC	kidney:	n/a	n/a
43	CTCF	chr10:631620-631770	AG09319	gingival:	n/a	n/a
44	CTCF	chr10:631560-631710	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr10:631880-632030	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr10:634191-634308	HepG2	liver:	n/a	n/a
47	CTCF	chr10:619380-619530	HAc	cerebellar:	n/a	n/a
48	CTCF	chr10:634180-634330	AG09309	skin:	n/a	n/a
49	CTCF	chr10:631740-631890	AG04450	lung:	n/a	n/a
50	CTCF	chr10:619340-619490	HEEpiC	esophagus:	n/a	n/a

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:630310-630360	NHDF-neo	bronchial:	n/a
2	chr10:630310-630360	U87	brain:	n/a
3	chr10:630310-630360	NHDF-neo	bronchial:	n/a
4	chr10:630310-630360	U87	brain:	n/a
5	chr10:612314-612364	NT2-D1	testis:	n/a
6	chr10:636390-636440	SK-N-MC	brain:	n/a
7	chr10:630310-630360	AG09309	skin:	n/a
8	chr10:640061-640111	HIPEpiC	eye:	n/a
9	chr10:640061-640111	SAEC	small airway:	n/a
10	chr10:636140-636190	HCPEpiC	choroid plexus:	n/a
11	chr10:630671-630721	HL-60	blood:	n/a
12	chr10:612391-612441	U87	brain:	n/a
13	chr10:636140-636190	PFSK-1	brain:	n/a
14	chr10:629582-629632	BE2_C	brain:	n/a
15	chr10:636331-636381	HMEC	breast:	n/a
16	chr10:636390-636440	HRPEpiC	eye:	n/a
17	chr10:630942-630992	HMEC	breast:	n/a
18	chr10:612391-612441	BJ	skin:	n/a
19	chr10:630671-630721	GM19239	blood:	n/a
20	chr10:623056-623106	AG10803	skin:	n/a
21	chr10:640996-641046	AG09309	skin:	n/a
22	chr10:627679-627729	HNPCEpiC	eye:	n/a
23	chr10:636140-636190	AG10803	skin:	n/a
24	chr10:640996-641046	AG04450	lung:	fetal
25	chr10:636076-636126	A549	lung:	n/a
26	chr10:630310-630360	SK-N-MC	brain:	n/a
27	chr10:640738-640788	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:612391-612441	AG09309	skin:	n/a
29	chr10:616959-617009	HRPEpiC	eye:	n/a
30	chr10:640770-640820	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:623056-623106	HCPEpiC	choroid plexus:	n/a
32	chr10:616995-617045	HPAEpiC	pulmonary alveolar:	n/a
33	chr10:612266-612316	HMEC	breast:	n/a
34	chr10:639935-639985	AG04449	skin:	fetal
35	chr10:636390-636440	Hela-S3	cervix:	n/a
36	chr10:630942-630992	U87	brain:	n/a
37	chr10:636241-636291	HRPEpiC	eye:	n/a
38	chr10:612391-612441	NHBE	bronchial:	n/a
39	chr10:612314-612364	NHDF-neo	bronchial:	n/a
40	chr10:640770-640820	ECC-1	luminal epithelium:	n/a
41	chr10:616995-617045	HCM	heart:	n/a
42	chr10:636241-636291	H1-hESC	embryonic stem cell:	embryo
43	chr10:630384-630434	HCT-116	colon:	n/a
44	chr10:629565-629615	HUVEC	blood vessel:	n/a
45	chr10:639935-639985	HUVEC	blood vessel:	n/a
46	chr10:636140-636190	AG09309	skin:	n/a
47	chr10:630310-630360	GM06990	blood:	n/a
48	chr10:616995-617045	Jurkat	blood:	n/a
49	chr10:640770-640820	HEEpiC	esophagus:	n/a
50	chr10:632914-632964	T-47D	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
2	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
3	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
4	chr10:627398..630591-chr10:632947..634840,3	K562	blood:
5	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
6	chr10:631818..632398-chr3:122337364..122338295,2	MCF-7	breast:
7	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
8	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
9	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
10	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
11	chr10:638624..640408-chr10:644679..647011,2	MCF-7	breast:
12	chr10:634649..636667-chr10:654000..655714,2	MCF-7	breast:
13	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
14	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
15	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
16	chr10:641312..643673-chr10:645720..648516,2	MCF-7	breast:
17	chr10:632878..635792-chr10:829676..832349,2	MCF-7	breast:
18	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
19	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
20	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
21	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
22	chr10:629648..631897-chr10:633164..636396,3	MCF-7	breast:
23	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
24	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
25	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
26	chr10:636273..639205-chr10:641067..642739,2	MCF-7	breast:
27	chr10:636273..639205-chr10:641067..642739,2	MCF-7	breast:
28	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
29	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
30	chr10:630264..632276-chr10:643488..645388,2	MCF-7	breast:
31	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:

No data

Variant related genes	Relation type
DIP2C	TF binding region
DIP2C	CpG island
ENSG00000151240	chromatin interactions

Extended variants
information (count: 2406 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550916712	chr10:606330-606331	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141953149	chr10:606348-606349	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377673663	chr10:606349-606350	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115200554	chr10:606417-606418	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552980508	chr10:606484-606485	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367906147	chr10:606485-606486	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139783642	chr10:606493-606494	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547282731	chr10:606495-606496	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12572372	chr10:606500-606501	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532904082	chr10:606516-606517	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145281224	chr10:606549-606550	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182143094	chr10:606559-606560	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569340172	chr10:606586-606587	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565025893	chr10:606609-606610	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530420764	chr10:606622-606623	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544199465	chr10:606669-606670	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561206732	chr10:606683-606684	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535129658	chr10:606687-606688	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12265680	chr10:606705-606706	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368659835	chr10:606733-606734	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145024276	chr10:606750-606751	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532778593	chr10:606751-606752	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371062909	chr10:606760-606761	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565937281	chr10:606803-606804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568672393	chr10:606836-606837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184553244	chr10:606846-606847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569377642	chr10:606869-606870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534358008	chr10:606882-606883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537801877	chr10:606891-606892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558154095	chr10:606902-606903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2605905	chr10:606908-606909	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs567531334	chr10:606912-606913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200101432	chr10:606915-606916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377626880	chr10:606920-606921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543166857	chr10:606926-606927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148662010	chr10:606927-606928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577405443	chr10:606942-606943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553330818	chr10:606981-606982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189000711	chr10:606992-606993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142139081	chr10:607033-607034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558322565	chr10:607041-607042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373973245	chr10:607062-607063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558964252	chr10:607091-607092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560573708	chr10:607105-607106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574125370	chr10:607113-607114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35066065	chr10:607117-607118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540511778	chr10:607125-607126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560455777	chr10:607153-607154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374978772	chr10:607175-607176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565436643	chr10:607213-607214	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	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
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
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD

Chromatin state (count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:598000-607400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:600400-608000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:600600-608000	Enhancers	Left Ventricle	heart
4	chr10:601000-610000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:601600-613600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr10:602400-609600	Enhancers	Brain Substantia Nigra	brain
7	chr10:602600-606400	Enhancers	Brain Hippocampus Middle	brain
8	chr10:602600-609200	Enhancers	Fetal Muscle Leg	muscle
9	chr10:602800-606400	Enhancers	Ovary	ovary
10	chr10:603000-606400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr10:603400-606600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:603400-607200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:603600-609800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:604000-606800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr10:604000-607200	Enhancers	Placenta	Placenta
16	chr10:604000-609400	Enhancers	Fetal Brain Male	brain
17	chr10:604200-607600	Weak transcription	Adipose Nuclei	Adipose
18	chr10:604400-606600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr10:604400-607400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr10:604400-607800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr10:604400-608800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr10:604600-607400	Weak transcription	Spleen	Spleen
23	chr10:604600-609000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr10:605000-606400	Enhancers	NH-A	brain
25	chr10:605000-606800	Enhancers	Lung	lung
26	chr10:605200-606400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:605200-606600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr10:605200-607000	Enhancers	Stomach Mucosa	stomach
29	chr10:605200-608200	Enhancers	Brain Angular Gyrus	brain
30	chr10:605200-608200	Enhancers	Pancreas	Pancrea
31	chr10:605200-609600	Enhancers	Colon Smooth Muscle	Colon
32	chr10:605400-606400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr10:605400-606800	Enhancers	Brain Germinal Matrix	brain
34	chr10:605400-607000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr10:605400-608000	Weak transcription	Fetal Heart	heart
36	chr10:605400-608200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr10:605400-608200	Enhancers	Brain Anterior Caudate	brain
38	chr10:605600-606400	Enhancers	Gastric	stomach
39	chr10:605600-606400	Enhancers	HepG2	liver
40	chr10:605600-607200	Enhancers	Fetal Lung	lung
41	chr10:605600-608200	Enhancers	Right Ventricle	heart
42	chr10:605600-608600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr10:605600-608800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr10:605600-609200	Enhancers	Brain Cingulate Gyrus	brain
45	chr10:605800-606600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr10:605800-606600	Weak transcription	Right Atrium	heart
47	chr10:605800-606600	Weak transcription	A549	lung
48	chr10:605800-608600	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr10:605800-608800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr10:605800-610000	Weak transcription	Fetal Stomach	stomach

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