Variant report

Variant	esv3459772
Chromosome Location	chr2:128103655-128114047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:287)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:287 , 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	ARID3A	chr2:128112985-128113318	K562	blood:	n/a	n/a
2	CEBPB	chr2:128111929-128112177	HepG2	liver:	n/a	chr2:128112033-128112044
3	CEBPB	chr2:128111877-128112218	Hela-S3	cervix:	n/a	chr2:128111920-128111932 chr2:128112033-128112044
4	CEBPB	chr2:128106134-128106421	MCF-7	breast:	n/a	chr2:128106245-128106256
5	CEBPB	chr2:128106112-128106401	Hela-S3	cervix:	n/a	chr2:128106245-128106256
6	CEBPB	chr2:128111856-128112292	MCF-7	breast:	n/a	chr2:128111920-128111932 chr2:128112033-128112044
7	CEBPB	chr2:128106090-128106392	A549	lung:	n/a	chr2:128106245-128106256
8	CEBPB	chr2:128105510-128105706	HepG2	liver:	n/a	chr2:128105658-128105669
9	CEBPB	chr2:128105507-128105685	A549	lung:	n/a	chr2:128105658-128105669
10	CEBPB	chr2:128106086-128106420	K562	blood:	n/a	chr2:128106245-128106256
11	CEBPB	chr2:128111871-128112183	MCF-7	breast:	n/a	chr2:128111920-128111932 chr2:128112033-128112044
12	CEBPB	chr2:128106064-128106403	IMR90	lung:	n/a	chr2:128106245-128106256
13	CEBPB	chr2:128104697-128104901	A549	lung:	n/a	n/a
14	CEBPB	chr2:128106107-128106397	HepG2	liver:	n/a	chr2:128106245-128106256
15	CEBPD	chr2:128112961-128113458	K562	blood:	n/a	n/a
16	CTCF	chr2:128113140-128113290	GM12865	blood:	n/a	n/a
17	CTCF	chr2:128113126-128113271	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:128113023-128113307	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:128113098-128113279	HepG2	liver:	n/a	n/a
20	CTCF	chr2:128113060-128113273	GM10248	blood:	n/a	n/a
21	CTCF	chr2:128113086-128113287	GM10266	blood:	n/a	n/a
22	CTCF	chr2:128113108-128113300	GM19238	blood:	n/a	n/a
23	CTCF	chr2:128113106-128113258	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr2:128113100-128113250	HEK293	kidney:	n/a	n/a
25	CTCF	chr2:128112838-128112936	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr2:128111816-128113831	A549	lung:	n/a	n/a
27	CTCF	chr2:128112916-128113412	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:128113140-128113290	GM12864	blood:	n/a	n/a
29	CTCF	chr2:128113100-128113250	GM12871	blood:	n/a	n/a
30	CTCF	chr2:128112700-128112850	HPF	lung:	n/a	n/a
31	CTCF	chr2:128113086-128113305	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:128113140-128113290	HRE	kidney:	n/a	n/a
33	CTCF	chr2:128112800-128112950	AG04450	lung:	n/a	n/a
34	CTCF	chr2:128113080-128113230	HMEC	breast:	n/a	n/a
35	CTCF	chr2:128113100-128113250	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr2:128113120-128113270	GM12868	blood:	n/a	n/a
37	CTCF	chr2:128113100-128113250	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr2:128113100-128113250	GM12868	blood:	n/a	n/a
39	CTCF	chr2:128113080-128113230	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr2:128113180-128113330	HVMF	connective:	n/a	n/a
41	CTCF	chr2:128112740-128113577	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr2:128113080-128113230	HepG2	liver:	n/a	n/a
43	CTCF	chr2:128113463-128113503	LNCaP	prostate:	n/a	n/a
44	CTCF	chr2:128113101-128113253	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr2:128113120-128113270	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:128113009-128113356	A549	lung:	n/a	n/a
47	CTCF	chr2:128113081-128113295	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:128113100-128113250	HL-60	blood:	n/a	n/a
49	CTCF	chr2:128112740-128112890	AG09309	skin:	n/a	n/a
50	CTCF	chr2:128113120-128113270	GM12873	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:128110833-128110883	HCT-116	colon:	n/a
2	chr2:128110833-128110883	GM06990	blood:	n/a
3	chr2:128110833-128110883	HAEpiC	amniotic membrane:	n/a
4	chr2:128110833-128110883	AG04449	skin:	fetal
5	chr2:128110833-128110883	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:128110833-128110883	AG04450	lung:	fetal
7	chr2:128110833-128110883	HNPCEpiC	eye:	n/a
8	chr2:128110833-128110883	HMEC	breast:	n/a
9	chr2:128110833-128110883	NB4	blood:	n/a
10	chr2:128110833-128110883	HL-60	blood:	n/a
11	chr2:128110833-128110883	HEEpiC	esophagus:	n/a
12	chr2:128110833-128110883	Hepatocyte	liver:	n/a
13	chr2:128110833-128110883	GM12878	blood:	n/a
14	chr2:128110833-128110883	U87	brain:	n/a
15	chr2:128110833-128110883	K562	blood:	n/a
16	chr2:128110833-128110883	AoSMC	blood vessel:	n/a
17	chr2:128110833-128110883	NHBE	bronchial:	n/a
18	chr2:128110833-128110883	RPTEC	kidney:	n/a
19	chr2:128110833-128110883	ECC-1	luminal epithelium:	n/a
20	chr2:128110833-128110883	LNCaP	prostate:	n/a
21	chr2:128110833-128110883	SK-N-SH	brain:	n/a
22	chr2:128110833-128110883	PANC-1	pancreas:	n/a
23	chr2:128110833-128110883	HRPEpiC	eye:	n/a
24	chr2:128110833-128110883	MCF-7	breast:	n/a
25	chr2:128110833-128110883	HCF	heart:	n/a
26	chr2:128110833-128110883	HCM	heart:	n/a
27	chr2:128110833-128110883	SK-N-MC	brain:	n/a
28	chr2:128110833-128110883	BJ	skin:	n/a
29	chr2:128110833-128110883	AG10803	skin:	n/a
30	chr2:128110833-128110883	SAEC	small airway:	n/a
31	chr2:128110833-128110883	SK-N-SH_RA	brain:	n/a
32	chr2:128110833-128110883	Jurkat	blood:	n/a
33	chr2:128110833-128110883	A549	lung:	n/a
34	chr2:128110833-128110883	HepG2	liver:	n/a
35	chr2:128110833-128110883	HIPEpiC	eye:	n/a
36	chr2:128110833-128110883	SKMC	muscle:	n/a
37	chr2:128110833-128110883	NH-A	brain:	n/a
38	chr2:128110833-128110883	GM12891	blood:	n/a
39	chr2:128110833-128110883	ProgFib	skin:	n/a
40	chr2:128110833-128110883	NT2-D1	testis:	n/a
41	chr2:128110833-128110883	MCF10A-Er-Src	breast:	n/a
42	chr2:128110833-128110883	HRE	kidney:	n/a
43	chr2:128110833-128110883	PFSK-1	brain:	n/a
44	chr2:128110833-128110883	H1-hESC	embryonic stem cell:	embryo
45	chr2:128110833-128110883	GM12892	blood:	n/a
46	chr2:128110833-128110883	AG09319	gingival:	n/a
47	chr2:128110833-128110883	PrEC	prostate:	n/a
48	chr2:128110833-128110883	HUVEC	blood vessel:	n/a
49	chr2:128110833-128110883	Caco-2	colon:	n/a
50	chr2:128110833-128110883	AG09309	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:128112029..128113592-chr2:128144594..128147259,2	MCF-7	breast:
2	chr2:128112789..128113667-chr2:128211064..128211727,2	MCF-7	breast:
3	chr2:128112592..128115294-chr2:128140839..128143680,2	MCF-7	breast:
4	chr2:128103044..128106466-chr2:128144475..128146523,3	MCF-7	breast:
5	chr2:128104503..128107403-chr2:128143958..128146297,2	MCF-7	breast:
6	chr2:128112156..128113664-chr2:128210673..128211919,7	MCF-7	breast:
7	chr2:128112442..128114326-chr2:128127386..128129324,2	MCF-7	breast:
8	chr2:128107155..128109690-chr2:128143179..128145881,2	MCF-7	breast:
9	chr2:128111305..128113465-chr2:128157702..128159726,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAP3K2	TF binding region
MAP3K2	CpG island
ENSG00000236682	chromatin interactions
ENSG00000169967	chromatin interactions

Extended variants
information (count: 429 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540734472	chr2:128103661-128103662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs10928763	chr2:128103714-128103715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs10928764	chr2:128103801-128103802	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs555638762	chr2:128103804-128103805	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554367210	chr2:128103809-128103810	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572257892	chr2:128103850-128103851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183722988	chr2:128103869-128103870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185530973	chr2:128103900-128103901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576323191	chr2:128103903-128103904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs202238262	chr2:128103983-128103984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572613234	chr2:128103986-128103987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201816351	chr2:128103987-128103988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377130638	chr2:128104009-128104010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs532070542	chr2:128104023-128104024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548557698	chr2:128104048-128104049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534946687	chr2:128104153-128104154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141299050	chr2:128104181-128104182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150721747	chr2:128104191-128104192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs62157554	chr2:128104284-128104285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs200283996	chr2:128104318-128104319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190431149	chr2:128104320-128104321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145364929	chr2:128104321-128104322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139062326	chr2:128104348-128104349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72845988	chr2:128104522-128104523	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149878101	chr2:128104528-128104529	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535752577	chr2:128104553-128104554	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555326995	chr2:128104554-128104555	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200280356	chr2:128104571-128104572	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13393193	chr2:128104594-128104595	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13419451	chr2:128104597-128104598	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572221242	chr2:128104621-128104622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112922811	chr2:128104630-128104631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539478492	chr2:128104633-128104634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs557961349	chr2:128104687-128104688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577458820	chr2:128104757-128104758	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546308877	chr2:128104787-128104788	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371669646	chr2:128104803-128104804	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374789949	chr2:128104807-128104808	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs72845989	chr2:128104821-128104822	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs542529072	chr2:128104822-128104823	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs139856054	chr2:128104850-128104851	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182265195	chr2:128104886-128104887	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144413506	chr2:128104914-128104915	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564338289	chr2:128104971-128104972	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs532905867	chr2:128105007-128105008	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146597925	chr2:128105046-128105047	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532287675	chr2:128105056-128105057	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186929847	chr2:128105071-128105072	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528855690	chr2:128105077-128105078	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548948699	chr2:128105084-128105085	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:128059400-128109600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:128069000-128117000	Weak transcription	Small Intestine	intestine
3	chr2:128072200-128109600	Weak transcription	Esophagus	oesophagus
4	chr2:128072200-128111800	Weak transcription	K562	blood
5	chr2:128072600-128112000	Weak transcription	NHEK	skin
6	chr2:128074800-128106800	Weak transcription	Spleen	Spleen
7	chr2:128077000-128116200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:128077200-128122800	Weak transcription	Aorta	Aorta
9	chr2:128078600-128109600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:128078800-128105400	Weak transcription	HSMMtube	muscle
11	chr2:128079400-128107800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:128079800-128107600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr2:128079800-128114600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:128082000-128105200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr2:128082000-128114600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr2:128083600-128105400	Weak transcription	Brain Substantia Nigra	brain
17	chr2:128083600-128117000	Weak transcription	Brain Anterior Caudate	brain
18	chr2:128086600-128112000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr2:128088800-128109400	Weak transcription	Right Ventricle	heart
20	chr2:128090800-128112000	Weak transcription	Rectal Smooth Muscle	rectum
21	chr2:128092600-128104400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:128092600-128109400	Weak transcription	Lung	lung
23	chr2:128092600-128122000	Weak transcription	Pancreas	Pancrea
24	chr2:128092800-128109600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr2:128093200-128122800	Weak transcription	Fetal Kidney	kidney
26	chr2:128093400-128106800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr2:128093400-128107400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr2:128094800-128106800	Weak transcription	Gastric	stomach
29	chr2:128095600-128122000	Weak transcription	Brain Angular Gyrus	brain
30	chr2:128096200-128105400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr2:128096200-128105800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:128096200-128106200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr2:128096400-128105400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr2:128096400-128109000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr2:128096400-128109400	Weak transcription	Ovary	ovary
36	chr2:128096400-128112000	Weak transcription	Brain Hippocampus Middle	brain
37	chr2:128096400-128122200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:128096600-128105400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr2:128096800-128117800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr2:128096800-128119600	Weak transcription	HSMM	muscle
41	chr2:128097000-128105400	Weak transcription	Adipose Nuclei	Adipose
42	chr2:128098000-128106200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:128098200-128105400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr2:128099000-128109400	Weak transcription	Right Atrium	heart
45	chr2:128100000-128104400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr2:128100000-128104400	Weak transcription	Fetal Stomach	stomach
47	chr2:128100000-128112000	Weak transcription	Fetal Lung	lung
48	chr2:128100200-128104800	Weak transcription	Primary hematopoietic stem cells	blood
49	chr2:128100200-128109600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:128100200-128110000	Weak transcription	Fetal Intestine Large	intestine

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