Variant report

Variant	nsv527312
Chromosome Location	chr10:618685-641961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:279)
CpG islands
(count:1587)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:279 , 50 per page) page: 1 2 3 4 5 6

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	chr10:640267-640478	A549	lung:	n/a	n/a
5	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
6	CTCF	chr10:634200-634350	GM06990	blood:	n/a	n/a
7	CTCF	chr10:634160-634310	HAc	cerebellar:	n/a	n/a
8	CTCF	chr10:634180-634302	NHEK	skin:	n/a	n/a
9	CTCF	chr10:637580-637730	GM12866	blood:	n/a	n/a
10	CTCF	chr10:633512-634343	A549	lung:	n/a	n/a
11	CTCF	chr10:634202-634270	GM19239	blood:	n/a	n/a
12	CTCF	chr10:619316-619506	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr10:631520-631670	HepG2	liver:	n/a	n/a
14	CTCF	chr10:619282-619694	K562	blood:	n/a	n/a
15	CTCF	chr10:634220-634370	WI-38	lung:	n/a	n/a
16	CTCF	chr10:634160-634310	HepG2	liver:	n/a	n/a
17	CTCF	chr10:619302-619504	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:631596-631739	K562	blood:	n/a	n/a
19	CTCF	chr10:631880-632030	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr10:634160-634310	AG04449	skin:	n/a	n/a
21	CTCF	chr10:619320-619470	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:634160-634310	NHLF	lung:	n/a	n/a
23	CTCF	chr10:634260-634410	A549	lung:	n/a	n/a
24	CTCF	chr10:634160-634310	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:634140-634290	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr10:634203-634276	GM19238	blood:	n/a	n/a
27	CTCF	chr10:632040-632190	HAc	cerebellar:	n/a	n/a
28	CTCF	chr10:634180-634330	AG09309	skin:	n/a	n/a
29	CTCF	chr10:634180-634330	SAEC	small airway:	n/a	n/a
30	CTCF	chr10:631415-631834	T-47D	breast:	n/a	n/a
31	CTCF	chr10:634175-634287	K562	blood:	n/a	n/a
32	CTCF	chr10:634180-634330	HRE	kidney:	n/a	n/a
33	CTCF	chr10:634165-634310	HepG2	liver:	n/a	n/a
34	CTCF	chr10:634156-634320	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr10:634180-634330	HPF	lung:	n/a	n/a
36	CTCF	chr10:631540-631690	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr10:631516-631759	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:631501-631768	K562	blood:	n/a	n/a
39	CTCF	chr10:631391-631847	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr10:634200-634350	AG04449	skin:	n/a	n/a
41	CTCF	chr10:634180-634330	HMF	breast:	n/a	n/a
42	CTCF	chr10:619320-619470	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr10:631880-632030	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr10:619320-619470	HEK293	kidney:	n/a	n/a
45	CTCF	chr10:634160-634310	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr10:634125-634371	K562	blood:	n/a	n/a
47	CTCF	chr10:634218-634278	GM12878	blood:	n/a	n/a
48	CTCF	chr10:631560-631710	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr10:619380-619530	HepG2	liver:	n/a	n/a
50	CTCF	chr10:632002-632008	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:641615-641665	GM12891	blood:	n/a
2	chr10:641615-641665	GM12891	blood:	n/a
3	chr10:636331-636381	SK-N-SH_RA	brain:	n/a
4	chr10:629565-629615	SK-N-SH_RA	brain:	n/a
5	chr10:640738-640788	AG04450	lung:	fetal
6	chr10:627679-627729	U87	brain:	n/a
7	chr10:627679-627729	T-47D	breast:	n/a
8	chr10:636331-636381	HNPCEpiC	eye:	n/a
9	chr10:636076-636126	SK-N-MC	brain:	n/a
10	chr10:639935-639985	Hela-S3	cervix:	n/a
11	chr10:640996-641046	A549	lung:	n/a
12	chr10:636140-636190	HEK293	kidney:	embryo
13	chr10:641641-641691	HRPEpiC	eye:	n/a
14	chr10:636331-636381	HEEpiC	esophagus:	n/a
15	chr10:640085-640135	HCM	heart:	n/a
16	chr10:636331-636381	H1-hESC	embryonic stem cell:	embryo
17	chr10:630384-630434	HL-60	blood:	n/a
18	chr10:636331-636381	LNCaP	prostate:	n/a
19	chr10:629625-629675	K562	blood:	n/a
20	chr10:636241-636291	GM19239	blood:	n/a
21	chr10:631304-631354	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:633154-633204	HIPEpiC	eye:	n/a
23	chr10:630310-630360	Jurkat	blood:	n/a
24	chr10:641641-641691	A549	lung:	n/a
25	chr10:641641-641691	H1-hESC	embryonic stem cell:	embryo
26	chr10:623056-623106	HEEpiC	esophagus:	n/a
27	chr10:641641-641691	ovcar-3	ovarian:	n/a
28	chr10:631304-631354	CMK	blood:	n/a
29	chr10:632914-632964	HUVEC	blood vessel:	n/a
30	chr10:630310-630360	IMR90	lung:	fetal
31	chr10:630310-630360	PANC-1	pancreas:	n/a
32	chr10:631304-631354	MCF-7	breast:	n/a
33	chr10:640085-640135	PFSK-1	brain:	n/a
34	chr10:641615-641665	SK-N-SH	brain:	n/a
35	chr10:630671-630721	CMK	blood:	n/a
36	chr10:640061-640111	HEEpiC	esophagus:	n/a
37	chr10:640770-640820	HCPEpiC	choroid plexus:	n/a
38	chr10:641615-641665	HepG2	liver:	n/a
39	chr10:636241-636291	BJ	skin:	n/a
40	chr10:631304-631354	AoSMC	blood vessel:	n/a
41	chr10:640738-640788	SAEC	small airway:	n/a
42	chr10:641626-641676	GM12878	blood:	n/a
43	chr10:641641-641691	HCPEpiC	choroid plexus:	n/a
44	chr10:630384-630434	NHBE	bronchial:	n/a
45	chr10:630384-630434	MCF10A-Er-Src	breast:	n/a
46	chr10:629582-629632	SK-N-SH	brain:	n/a
47	chr10:636140-636190	HAEpiC	amniotic membrane:	n/a
48	chr10:636331-636381	T-47D	breast:	n/a
49	chr10:629582-629632	HL-60	blood:	n/a
50	chr10:636390-636440	AG04449	skin:	fetal

(count:26 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1761 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1761 , 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	rs17221323	chr10:618685-618686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs377679725	chr10:618689-618690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530062769	chr10:618704-618705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549574928	chr10:618724-618725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114396509	chr10:618782-618783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373135027	chr10:618806-618807	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs551500147	chr10:618828-618829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs547018415	chr10:618840-618841	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs7082405	chr10:618841-618842	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556143783	chr10:618855-618856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532486702	chr10:618867-618868	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs552382762	chr10:618885-618886	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374567098	chr10:618886-618887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148098563	chr10:618891-618892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs370201378	chr10:618895-618896	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs535268802	chr10:618911-618912	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs72774560	chr10:618925-618926	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs572305386	chr10:618942-618943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs541120670	chr10:618954-618955	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145758211	chr10:618959-618960	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs564171184	chr10:618983-618984	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs372598099	chr10:618990-618991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs377370286	chr10:618995-618996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs577670396	chr10:619004-619005	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs187281692	chr10:619022-619023	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs192665413	chr10:619032-619033	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs61831055	chr10:619035-619036	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549444909	chr10:619062-619063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs74115063	chr10:619078-619079	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528708993	chr10:619088-619089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs371897932	chr10:619094-619095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs184655774	chr10:619118-619119	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs816628	chr10:619170-619171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs144934179	chr10:619179-619180	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs550977113	chr10:619186-619187	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs189166822	chr10:619189-619190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs75756194	chr10:619239-619240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs182417815	chr10:619252-619253	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572222704	chr10:619258-619259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs534818861	chr10:619295-619296	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs17159691	chr10:619316-619317	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs566815440	chr10:619323-619324	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs79954097	chr10:619329-619330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs538981011	chr10:619344-619345	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs543180332	chr10:619346-619347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs556901342	chr10:619372-619373	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs573593972	chr10:619373-619374	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs543301783	chr10:619409-619410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs559624044	chr10:619426-619427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs528622500	chr10:619441-619442	Weak transcription Enhancers Flanking Active TSS	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:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:612800-620200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:614200-620400	Weak transcription	Pancreas	Pancrea
3	chr10:614200-621600	Weak transcription	Ovary	ovary
4	chr10:616000-621800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:616200-619000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:616200-622600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr10:616200-643800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:616400-619000	Enhancers	Fetal Muscle Leg	muscle
9	chr10:616400-619400	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:616400-619400	Enhancers	Placenta Amnion	Placenta Amnion
11	chr10:616400-623600	Enhancers	Brain Hippocampus Middle	brain
12	chr10:616600-619400	Enhancers	Fetal Lung	lung
13	chr10:616600-620000	Enhancers	Fetal Brain Male	brain
14	chr10:616600-621400	Weak transcription	Fetal Intestine Small	intestine
15	chr10:616600-621800	Enhancers	Brain Anterior Caudate	brain
16	chr10:616600-621800	Weak transcription	Esophagus	oesophagus
17	chr10:616600-622600	Enhancers	Brain Angular Gyrus	brain
18	chr10:616800-618800	Enhancers	Fetal Stomach	stomach
19	chr10:616800-619000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr10:616800-619000	Weak transcription	Fetal Kidney	kidney
21	chr10:616800-619600	Enhancers	Fetal Brain Female	brain
22	chr10:617000-619400	Enhancers	Brain Germinal Matrix	brain
23	chr10:617200-619400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:617200-623400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr10:617400-618800	Enhancers	Rectal Smooth Muscle	rectum
26	chr10:617400-620200	Enhancers	Brain Substantia Nigra	brain
27	chr10:617400-621400	Weak transcription	Stomach Mucosa	stomach
28	chr10:617400-622600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr10:617600-618800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr10:617600-619000	Enhancers	Left Ventricle	heart
31	chr10:617800-619200	Enhancers	Colon Smooth Muscle	Colon
32	chr10:617800-620600	Weak transcription	Gastric	stomach
33	chr10:617800-621800	Weak transcription	Fetal Thymus	thymus
34	chr10:617800-622000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr10:618000-620600	Weak transcription	Aorta	Aorta
36	chr10:618200-618800	Enhancers	Stomach Smooth Muscle	stomach
37	chr10:618200-619600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr10:618200-620800	Weak transcription	Lung	lung
39	chr10:618200-621200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:618200-621400	Weak transcription	Psoas Muscle	Psoas
41	chr10:618200-621600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:618200-621600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr10:618200-621600	Weak transcription	Right Atrium	heart
44	chr10:618200-622000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr10:618200-626200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr10:618400-620600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr10:618400-620600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:618400-620800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:618400-620800	Weak transcription	Adipose Nuclei	Adipose
50	chr10:618400-621000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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