Variant report

Variant	nsv584698
Chromosome Location	chr2:234107070-234118583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:394)
CpG islands
(count:428)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:234111096-234111501	GM12878	blood:	n/a	n/a
2	ATF2	chr2:234111018-234111683	GM12878	blood:	n/a	n/a
3	ATF2	chr2:234108434-234108969	GM12878	blood:	n/a	n/a
4	BATF	chr2:234110363-234110582	GM12878	blood:	n/a	chr2:234110479-234110488
5	BCL3	chr2:234111044-234111434	GM12878	blood:	n/a	n/a
6	BCL3	chr2:234111038-234111581	GM12878	blood:	n/a	n/a
7	BCL3	chr2:234113228-234113486	GM12878	blood:	n/a	n/a
8	BCL3	chr2:234113160-234113569	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:234108483-234108842	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:234111323-234111537	GM12878	blood:	n/a	n/a
11	CHD2	chr2:234117100-234117285	HepG2	liver:	n/a	n/a
12	CHD2	chr2:234111194-234111576	GM12878	blood:	n/a	n/a
13	CHD2	chr2:234117125-234117408	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:234108540-234108690	GM12872	blood:	n/a	n/a
15	CTCF	chr2:234117080-234117230	HMEC	breast:	n/a	chr2:234117122-234117131
16	CTCF	chr2:234116680-234116830	GM12875	blood:	n/a	chr2:234116821-234116829
17	CTCF	chr2:234108640-234108790	GM12866	blood:	n/a	n/a
18	CTCF	chr2:234108520-234108670	GM12878	blood:	n/a	n/a
19	CTCF	chr2:234118160-234118310	RPTEC	kidney:	n/a	chr2:234118271-234118279 chr2:234118264-234118282 chr2:234118266-234118279
20	CTCF	chr2:234117080-234117230	Hela-S3	cervix:	n/a	chr2:234117122-234117131
21	CTCF	chr2:234118211-234118343	MCF-7	breast:	n/a	chr2:234118271-234118279 chr2:234118264-234118282 chr2:234118266-234118279
22	CTCF	chr2:234117500-234117870	HRE	kidney:	n/a	n/a
23	CTCF	chr2:234108500-234108650	HAc	cerebellar:	n/a	n/a
24	CTCF	chr2:234117020-234117170	WERI-Rb-1	eye:	n/a	chr2:234117122-234117131
25	CTCF	chr2:234108600-234108750	GM12865	blood:	n/a	n/a
26	CTCF	chr2:234116981-234117323	K562	blood:	n/a	chr2:234117122-234117131
27	CTCF	chr2:234117076-234117202	GM12891	blood:	n/a	chr2:234117122-234117131
28	CTCF	chr2:234117040-234117190	GM12873	blood:	n/a	chr2:234117122-234117131
29	CTCF	chr2:234108635-234108706	K562	blood:	n/a	n/a
30	CTCF	chr2:234118232-234118317	MCF-7	breast:	n/a	chr2:234118271-234118279 chr2:234118264-234118282 chr2:234118266-234118279
31	CTCF	chr2:234108660-234108810	GM12875	blood:	n/a	n/a
32	CTCF	chr2:234108700-234108850	A549	lung:	n/a	n/a
33	CTCF	chr2:234118260-234118410	HepG2	liver:	n/a	chr2:234118271-234118279 chr2:234118264-234118282 chr2:234118266-234118279
34	CTCF	chr2:234108520-234108670	GM12868	blood:	n/a	n/a
35	CTCF	chr2:234108580-234108730	GM06990	blood:	n/a	n/a
36	CTCF	chr2:234116992-234117272	HepG2	liver:	n/a	chr2:234117122-234117131
37	CTCF	chr2:234117060-234117210	HCFaa	heart:	n/a	chr2:234117122-234117131
38	CTCF	chr2:234117040-234117190	Hela-S3	cervix:	n/a	chr2:234117122-234117131
39	CTCF	chr2:234117100-234117250	WERI-Rb-1	eye:	n/a	chr2:234117122-234117131
40	CTCF	chr2:234116940-234117090	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr2:234108540-234108690	GM06990	blood:	n/a	n/a
42	CTCF	chr2:234117073-234117172	HepG2	liver:	n/a	chr2:234117122-234117131
43	CTCF	chr2:234108520-234108670	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr2:234117020-234117170	HRPEpiC	eye:	n/a	chr2:234117122-234117131
45	CTCF	chr2:234117100-234117250	HCPEpiC	choroid plexus:	n/a	chr2:234117122-234117131
46	CTCF	chr2:234116980-234117130	A549	lung:	n/a	n/a
47	CTCF	chr2:234117580-234117730	HAc	cerebellar:	n/a	n/a
48	CTCF	chr2:234117020-234117170	GM06990	blood:	n/a	chr2:234117122-234117131
49	CTCF	chr2:234117060-234117210	GM12872	blood:	n/a	chr2:234117122-234117131
50	CTCF	chr2:234117740-234117890	A549	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234111145-234111195	CMK	blood:	n/a
2	chr2:234111145-234111195	CMK	blood:	n/a
3	chr2:234111145-234111195	HL-60	blood:	n/a
4	chr2:234113197-234113247	AG09319	gingival:	n/a
5	chr2:234113372-234113422	AG04450	lung:	fetal
6	chr2:234111145-234111195	NB4	blood:	n/a
7	chr2:234111145-234111195	LNCaP	prostate:	n/a
8	chr2:234111145-234111195	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:234113122-234113172	HEK293	kidney:	embryo
10	chr2:234113197-234113247	HNPCEpiC	eye:	n/a
11	chr2:234113122-234113172	Jurkat	blood:	n/a
12	chr2:234116266-234116316	HIPEpiC	eye:	n/a
13	chr2:234112793-234112843	GM12892	blood:	n/a
14	chr2:234112955-234113005	PANC-1	pancreas:	n/a
15	chr2:234116266-234116316	NT2-D1	testis:	n/a
16	chr2:234113372-234113422	SK-N-SH	brain:	n/a
17	chr2:234113372-234113422	SK-N-SH_RA	brain:	n/a
18	chr2:234112955-234113005	SK-N-MC	brain:	n/a
19	chr2:234112793-234112843	HRCEpiC	kidney:	n/a
20	chr2:234113122-234113172	GM12891	blood:	n/a
21	chr2:234111145-234111195	PANC-1	pancreas:	n/a
22	chr2:234116266-234116316	LNCaP	prostate:	n/a
23	chr2:234116266-234116316	NHBE	bronchial:	n/a
24	chr2:234111145-234111195	AoSMC	blood vessel:	n/a
25	chr2:234111145-234111195	HRPEpiC	eye:	n/a
26	chr2:234111145-234111195	GM12891	blood:	n/a
27	chr2:234113197-234113247	HCM	heart:	n/a
28	chr2:234112793-234112843	HUVEC	blood vessel:	n/a
29	chr2:234113122-234113172	HMEC	breast:	n/a
30	chr2:234112955-234113005	SK-N-SH	brain:	n/a
31	chr2:234111145-234111195	H1-hESC	embryonic stem cell:	embryo
32	chr2:234116266-234116316	Caco-2	colon:	n/a
33	chr2:234113372-234113422	HUVEC	blood vessel:	n/a
34	chr2:234112793-234112843	SK-N-SH	brain:	n/a
35	chr2:234113372-234113422	SKMC	muscle:	n/a
36	chr2:234113122-234113172	HCF	heart:	n/a
37	chr2:234113122-234113172	AG09309	skin:	n/a
38	chr2:234112793-234112843	MCF-7	breast:	n/a
39	chr2:234116266-234116316	SAEC	small airway:	n/a
40	chr2:234112793-234112843	HRPEpiC	eye:	n/a
41	chr2:234112793-234112843	Hepatocyte	liver:	n/a
42	chr2:234111145-234111195	MCF-7	breast:	n/a
43	chr2:234112793-234112843	HepG2	liver:	n/a
44	chr2:234116266-234116316	NB4	blood:	n/a
45	chr2:234113197-234113247	BE2_C	brain:	n/a
46	chr2:234113372-234113422	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:234113197-234113247	CMK	blood:	n/a
48	chr2:234116266-234116316	SK-N-MC	brain:	n/a
49	chr2:234111145-234111195	NT2-D1	testis:	n/a
50	chr2:234112793-234112843	IMR90	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:234108742..234111363-chr2:234117940..234120302,2	K562	blood:
2	chr2:234100503..234103423-chr2:234114433..234117348,2	K562	blood:
3	chr2:234107430..234110250-chr2:234115314..234117709,2	MCF-7	breast:
4	chr2:234107430..234110250-chr2:234115314..234117709,2	MCF-7	breast:
5	chr2:233739500..233741658-chr2:234118418..234121019,2	MCF-7	breast:
6	chr2:234115407..234117275-chr2:234117591..234119947,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG16L1-2	chr2:234113845-234114121	NONHSAT077460

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	INPP5D	hsa-miR-155-5p	chr2:234115874-234115881
2	INPP5D	hsa-miR-155-5p	chr2:234115859-234115881

Variant related genes	Relation type
INPP5D	TF binding region
RN7SL32P	TF binding region
ATG16L1	TF binding region
INPP5D	CpG island
RN7SL32P	CpG island
ATG16L1	CpG island
ENSG00000085978	chromatin interactions
ENSG00000182600	chromatin interactions

Extended variants
information (count: 529 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7569827	chr2:234107070-234107071	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573612638	chr2:234107114-234107115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542282449	chr2:234107144-234107145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559564325	chr2:234107170-234107171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144190615	chr2:234107229-234107230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544758237	chr2:234107273-234107274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572021147	chr2:234107285-234107286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564786262	chr2:234107293-234107294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370548986	chr2:234107295-234107296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534288869	chr2:234107319-234107320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6719549	chr2:234107368-234107369	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs560925515	chr2:234107370-234107371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113254134	chr2:234107387-234107388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530076344	chr2:234107409-234107410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188470128	chr2:234107451-234107452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540084107	chr2:234107469-234107470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567110776	chr2:234107545-234107546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544457551	chr2:234107552-234107553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552799394	chr2:234107556-234107557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181094286	chr2:234107576-234107577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113025518	chr2:234107587-234107588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537122345	chr2:234107601-234107602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375268723	chr2:234107613-234107614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558265751	chr2:234107617-234107618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6722529	chr2:234107618-234107619	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573670831	chr2:234107629-234107630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13417000	chr2:234107694-234107695	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552700418	chr2:234107701-234107702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573091574	chr2:234107705-234107706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13009927	chr2:234107707-234107708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544944935	chr2:234107725-234107726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191450043	chr2:234107748-234107749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371708732	chr2:234107760-234107761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575122628	chr2:234107765-234107766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12987734	chr2:234107769-234107770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544020943	chr2:234107799-234107800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182073374	chr2:234107819-234107820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530146070	chr2:234107834-234107835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376510754	chr2:234107836-234107837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555753795	chr2:234107851-234107852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13004987	chr2:234107861-234107862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12987778	chr2:234107863-234107864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573655392	chr2:234107870-234107871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560330020	chr2:234107889-234107890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13025756	chr2:234107905-234107906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552933961	chr2:234107947-234107948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12987960	chr2:234107954-234107955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13010595	chr2:234107994-234107995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75121169	chr2:234108000-234108001	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13010610	chr2:234108011-234108012	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234053800-234110800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr2:234053800-234113800	Strong transcription	Primary T cells from cord blood	blood
3	chr2:234053800-234118000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:234054400-234110600	Weak transcription	Small Intestine	intestine
5	chr2:234055200-234113400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:234062000-234108400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:234074200-234111200	Weak transcription	Brain Substantia Nigra	brain
8	chr2:234074600-234122000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr2:234075200-234111800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:234075200-234117000	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr2:234075400-234111200	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr2:234075400-234113800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr2:234075400-234115200	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr2:234077200-234117200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:234078200-234110000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:234085200-234107200	Strong transcription	Thymus	Thymus
17	chr2:234089000-234111200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr2:234089000-234111400	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:234089200-234111400	Weak transcription	Left Ventricle	heart
20	chr2:234089400-234111000	Strong transcription	Fetal Thymus	thymus
21	chr2:234090200-234113800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
22	chr2:234091400-234111200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:234091800-234111200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr2:234092800-234107400	Strong transcription	Lung	lung
25	chr2:234094000-234111400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:234095000-234107400	Strong transcription	Adipose Nuclei	Adipose
27	chr2:234095200-234110800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr2:234095200-234111200	Weak transcription	Brain Hippocampus Middle	brain
29	chr2:234095200-234111600	Weak transcription	Brain Anterior Caudate	brain
30	chr2:234095800-234107400	Strong transcription	GM12878-XiMat	blood
31	chr2:234095800-234109800	Strong transcription	Primary B cells from peripheral blood	blood
32	chr2:234098200-234109800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:234098400-234107200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr2:234098600-234108600	Strong transcription	Spleen	Spleen
35	chr2:234098800-234109000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr2:234099200-234111400	Weak transcription	Right Ventricle	heart
37	chr2:234099600-234109600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:234099800-234109800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:234099800-234116000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr2:234100200-234110400	Strong transcription	Primary B cells from cord blood	blood
41	chr2:234100400-234121800	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr2:234100600-234108400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr2:234100800-234108600	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr2:234100800-234108600	Weak transcription	Fetal Stomach	stomach
45	chr2:234100800-234110000	Weak transcription	Esophagus	oesophagus
46	chr2:234101000-234109000	Weak transcription	Liver	Liver
47	chr2:234101000-234116000	Weak transcription	HUVEC	blood vessel
48	chr2:234101800-234107400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
49	chr2:234102400-234107200	Strong transcription	HepG2	liver
50	chr2:234102400-234107400	Strong transcription	Primary hematopoietic stem cells	blood

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