Variant report

Variant	esv1792752
Chromosome Location	chr7:17853983-17908546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17853694-17854015	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17855043-17855259	HepG2	liver:	n/a	n/a
3	ATF3	chr7:17854938-17855347	HepG2	liver:	n/a	n/a
4	BATF	chr7:17871956-17872120	GM12878	blood:	n/a	n/a
5	BATF	chr7:17871903-17872115	GM12878	blood:	n/a	chr7:17871948-17871957
6	BATF	chr7:17894938-17895167	GM12878	blood:	n/a	n/a
7	BATF	chr7:17883700-17883943	GM12878	blood:	n/a	n/a
8	BATF	chr7:17883672-17883959	GM12878	blood:	n/a	n/a
9	BATF	chr7:17894311-17894607	GM12878	blood:	n/a	n/a
10	BATF	chr7:17894349-17894613	GM12878	blood:	n/a	n/a
11	BATF	chr7:17898844-17899093	GM12878	blood:	n/a	n/a
12	BATF	chr7:17898772-17899044	GM12878	blood:	n/a	n/a
13	CEBPB	chr7:17855038-17855296	H1-hESC	embryonic stem cell:	n/a	chr7:17855158-17855169
14	CEBPB	chr7:17854910-17855278	HepG2	liver:	n/a	chr7:17855158-17855169
15	CEBPB	chr7:17869943-17870075	HepG2	liver:	n/a	chr7:17870003-17870016 chr7:17869968-17869985
16	CEBPB	chr7:17855019-17855320	HepG2	liver:	n/a	chr7:17855158-17855169
17	CEBPB	chr7:17855000-17855339	HepG2	liver:	n/a	chr7:17855158-17855169
18	CEBPB	chr7:17869897-17870122	Hela-S3	cervix:	n/a	chr7:17870003-17870016 chr7:17869968-17869985
19	CEBPB	chr7:17854952-17855320	MCF-7	breast:	n/a	chr7:17855158-17855169
20	CEBPB	chr7:17855070-17855232	A549	lung:	n/a	chr7:17855158-17855169
21	CEBPB	chr7:17854993-17855308	MCF-7	breast:	n/a	chr7:17855158-17855169
22	CEBPB	chr7:17855104-17855278	Hela-S3	cervix:	n/a	chr7:17855158-17855169
23	CEBPB	chr7:17854993-17855267	HepG2	liver:	n/a	chr7:17855158-17855169
24	CEBPD	chr7:17854887-17855229	HepG2	liver:	n/a	n/a
25	CTCF	chr7:17903347-17903387	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:17901600-17901750	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr7:17887715-17887732	GM10266	blood:	n/a	n/a
28	CTCF	chr7:17901580-17901730	BE2_C	brain:	n/a	n/a
29	CTCF	chr7:17901500-17901735	GM12878	blood:	n/a	n/a
30	CTCF	chr7:17901635-17901660	GM12878	blood:	n/a	n/a
31	CTCF	chr7:17903520-17903670	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr7:17869520-17869670	Caco-2	colon:	n/a	n/a
33	CTCF	chr7:17903420-17903570	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr7:17903574-17903643	Medullo	brain:	n/a	n/a
35	CTCF	chr7:17901580-17901730	GM06990	blood:	n/a	n/a
36	CTCF	chr7:17901616-17901703	Lung_OC	lung:	n/a	n/a
37	CTCF	chr7:17901540-17901690	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr7:17901600-17901750	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:17901527-17901779	K562	blood:	n/a	n/a
40	CUX1	chr7:17898789-17898941	GM12878	blood:	n/a	n/a
41	CUX1	chr7:17884599-17884631	K562	blood:	n/a	n/a
42	CUX1	chr7:17883763-17883963	GM12878	blood:	n/a	n/a
43	E2F6	chr7:17854826-17855143	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr7:17883846-17883869	GM12878	blood:	n/a	n/a
45	EP300	chr7:17854939-17855365	HepG2	liver:	n/a	n/a
46	EP300	chr7:17898883-17898886	GM12878	blood:	n/a	n/a
47	EP300	chr7:17874007-17874147	K562	blood:	n/a	n/a
48	EP300	chr7:17854954-17855348	HepG2	liver:	n/a	n/a
49	FOS	chr7:17884371-17884489	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:17869910-17870117	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17864166..17867586-chr7:17869183..17871409,4	K562	blood:
2	chr7:17897387..17900281-chr7:17901948..17903936,2	K562	blood:
3	chr7:17882358..17885096-chr7:17950396..17953115,2	K562	blood:
4	chr7:17890085..17891646-chr7:17912028..17913718,2	MCF-7	breast:
5	chr7:17863336..17865666-chr7:17868902..17871409,2	K562	blood:
6	chr7:17861812..17864316-chr7:17866527..17868627,2	K562	blood:
7	chr7:17886413..17888051-chr7:17895636..17897500,2	MCF-7	breast:
8	chr7:17861690..17863309-chr7:17878312..17881070,2	K562	blood:
9	chr7:17872510..17875086-chr7:17979395..17981460,2	MCF-7	breast:
10	chr7:17901839..17903435-chr7:17980572..17982643,2	MCF-7	breast:
11	chr7:17853768..17855990-chr7:17915652..17917897,2	K562	blood:
12	chr7:17868673..17871500-chr7:17873119..17875470,2	K562	blood:
13	chr7:17886526..17888087-chr7:17888537..17890269,2	MCF-7	breast:
14	chr7:17856945..17858744-chr7:17859975..17861675,2	K562	blood:
15	chr7:17853387..17855220-chr7:17856862..17859241,2	K562	blood:
16	chr7:17853678..17855376-chr7:17978755..17981532,2	MCF-7	breast:
17	chr7:17886526..17888087-chr7:17888537..17890269,2	MCF-7	breast:
18	chr7:17865698..17868586-chr7:17873859..17875914,2	K562	blood:
19	chr7:17861690..17863309-chr7:17878312..17881070,2	K562	blood:
20	chr7:17863336..17865666-chr7:17868902..17871409,2	K562	blood:
21	chr7:17853387..17855220-chr7:17856862..17859241,2	K562	blood:
22	chr7:17861812..17864316-chr7:17866527..17868627,2	K562	blood:
23	chr7:17865698..17868586-chr7:17873859..17875914,2	K562	blood:
24	chr7:17886413..17888051-chr7:17895636..17897500,2	MCF-7	breast:
25	chr7:17864166..17867586-chr7:17869183..17871409,4	K562	blood:
26	chr7:17868673..17871500-chr7:17873119..17875470,2	K562	blood:
27	chr7:17897387..17900281-chr7:17901948..17903936,2	K562	blood:
28	chr7:17844492..17846186-chr7:17870318..17872913,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNX13	TF binding region
ENSG00000071189	chromatin interactions

Extended variants
information (count: 2040 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2040 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2723494	chr7:17853983-17853984	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs201624194	chr7:17853996-17853997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541318463	chr7:17853999-17854000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559164958	chr7:17854017-17854018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376042880	chr7:17854024-17854025	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146242406	chr7:17854033-17854034	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139335854	chr7:17854055-17854056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187399842	chr7:17854072-17854073	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530441777	chr7:17854109-17854110	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs114710238	chr7:17854180-17854181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575823792	chr7:17854181-17854182	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564085874	chr7:17854213-17854214	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528829506	chr7:17854224-17854225	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547262238	chr7:17854227-17854228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142863068	chr7:17854229-17854230	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192193668	chr7:17854302-17854303	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182704247	chr7:17854332-17854333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115330101	chr7:17854407-17854408	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375525827	chr7:17854415-17854416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187926861	chr7:17854439-17854440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373267046	chr7:17854442-17854443	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547989333	chr7:17854485-17854486	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375171339	chr7:17854509-17854510	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557915166	chr7:17854524-17854525	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2723501	chr7:17854532-17854533	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs189736889	chr7:17854536-17854537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372932522	chr7:17854538-17854539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552802025	chr7:17854548-17854549	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377142168	chr7:17854557-17854558	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34681614	chr7:17854570-17854571	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370308794	chr7:17854574-17854575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200319037	chr7:17854575-17854576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77003957	chr7:17854576-17854577	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201341302	chr7:17854590-17854591	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2723502	chr7:17854616-17854617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542546335	chr7:17854742-17854743	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569803946	chr7:17854795-17854796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2723504	chr7:17854833-17854834	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs2723505	chr7:17854849-17854850	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs542882513	chr7:17854881-17854882	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10268362	chr7:17854902-17854903	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs563964847	chr7:17854908-17854909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528046307	chr7:17854915-17854916	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576320469	chr7:17854949-17854950	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540928585	chr7:17854959-17854960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116079726	chr7:17854960-17854961	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544991147	chr7:17854965-17854966	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529525094	chr7:17854971-17854972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375957592	chr7:17854977-17854978	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551226378	chr7:17855015-17855016	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17812600-17887600	Weak transcription	Gastric	stomach
2	chr7:17813600-17879200	Weak transcription	HSMMtube	muscle
3	chr7:17817400-17887600	Weak transcription	Pancreas	Pancrea
4	chr7:17823200-17854400	Weak transcription	Lung	lung
5	chr7:17823600-17887600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:17824800-17861800	Weak transcription	Fetal Heart	heart
7	chr7:17825800-17887600	Weak transcription	Colonic Mucosa	Colon
8	chr7:17826400-17864000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:17827400-17877600	Weak transcription	Small Intestine	intestine
10	chr7:17832000-17862600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:17832000-17880600	Weak transcription	GM12878-XiMat	blood
12	chr7:17834000-17887800	Weak transcription	Right Ventricle	heart
13	chr7:17834200-17879400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:17834800-17888800	Weak transcription	Brain Substantia Nigra	brain
15	chr7:17837800-17855400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:17838800-17887600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr7:17839000-17932600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr7:17841000-17861000	Weak transcription	NHDF-Ad	bronchial
19	chr7:17841000-17862000	Weak transcription	HUVEC	blood vessel
20	chr7:17841200-17883800	Weak transcription	HMEC	breast
21	chr7:17841200-17902600	Weak transcription	Brain Anterior Caudate	brain
22	chr7:17841400-17862200	Weak transcription	NH-A	brain
23	chr7:17841400-17862200	Weak transcription	NHEK	skin
24	chr7:17841400-17862800	Weak transcription	Stomach Mucosa	stomach
25	chr7:17841600-17879400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr7:17843200-17881800	Weak transcription	A549	lung
27	chr7:17843400-17864000	Weak transcription	Osteobl	bone
28	chr7:17843400-17864600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:17843400-17879200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:17846000-17900600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:17847400-17854800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr7:17847400-17862200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:17847400-17879000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:17847400-17880600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr7:17847400-17887600	Weak transcription	Ovary	ovary
36	chr7:17847400-17887600	Weak transcription	Spleen	Spleen
37	chr7:17847600-17887600	Weak transcription	Fetal Stomach	stomach
38	chr7:17847800-17862200	Weak transcription	Fetal Intestine Large	intestine
39	chr7:17847800-17864200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:17851400-17865400	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr7:17852000-17855600	Strong transcription	Primary B cells from peripheral blood	blood
42	chr7:17852000-17855800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:17852200-17854000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:17852200-17854600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr7:17852200-17855200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:17852200-17856000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:17852400-17854000	Strong transcription	Dnd41	blood
48	chr7:17852400-17854800	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr7:17852400-17855200	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:17852400-17855800	Strong transcription	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links