Variant report

Variant	esv3388387
Chromosome Location	chr2:86362741-86366539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:86365758-86366310	A549	lung:	n/a	n/a
2	CEBPB	chr2:86364094-86364280	HepG2	liver:	n/a	chr2:86364238-86364249
3	CTCF	chr2:86362820-86362970	HepG2	liver:	n/a	n/a
4	E2F4	chr2:86366439-86366542	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr2:86366334-86366367	MCF10A-Er-Src	breast:	n/a	n/a
6	MXI1	chr2:86363767-86363842	H1-hESC	embryonic stem cell:	n/a	n/a
7	MYC	chr2:86364991-86365013	MCF-7	breast:	n/a	n/a
8	MYC	chr2:86364974-86365037	MCF-7	breast:	n/a	n/a
9	POLR2A	chr2:86365692-86366183	U87	brain:	n/a	n/a
10	POLR2A	chr2:86364887-86365590	U87	brain:	n/a	n/a
11	POLR2A	chr2:86366130-86366147	MCF-7	breast:	n/a	n/a
12	POLR2A	chr2:86362925-86363041	A549	lung:	n/a	n/a
13	POLR2A	chr2:86365478-86365806	PFSK-1	brain:	n/a	n/a
14	POLR2A	chr2:86366314-86367286	GM12891	blood:	n/a	n/a
15	POLR2A	chr2:86365759-86369447	PANC-1	pancreas:	n/a	n/a
16	POLR2A	chr2:86366158-86367294	GM12892	blood:	n/a	n/a
17	POLR2A	chr2:86364795-86369338	GM12891	blood:	n/a	n/a
18	POLR2A	chr2:86365011-86365464	U87	brain:	n/a	n/a
19	POLR2A	chr2:86363828-86363856	MCF-7	breast:	n/a	n/a
20	POLR2A	chr2:86364898-86364910	K562	blood:	n/a	n/a
21	POLR2A	chr2:86365361-86366084	GM12878	blood:	n/a	n/a
22	POLR2A	chr2:86364514-86365264	GM12878	blood:	n/a	n/a
23	POLR2A	chr2:86362799-86363151	K562	blood:	n/a	n/a
24	POLR2A	chr2:86365011-86365484	U87	brain:	n/a	n/a
25	POLR2A	chr2:86365286-86365693	GM12892	blood:	n/a	n/a
26	POLR2A	chr2:86365874-86366321	K562	blood:	n/a	n/a
27	POLR2A	chr2:86364918-86365083	K562	blood:	n/a	n/a
28	POLR2A	chr2:86362177-86363090	HepG2	liver:	n/a	n/a
29	POLR2A	chr2:86365776-86366518	GM12891	blood:	n/a	n/a
30	POLR2A	chr2:86365516-86365753	K562	blood:	n/a	n/a
31	POLR2A	chr2:86364076-86364288	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr2:86363936-86364250	K562	blood:	n/a	n/a
33	POLR2A	chr2:86364907-86365108	A549	lung:	n/a	n/a
34	POLR2A	chr2:86363637-86364201	K562	blood:	n/a	n/a
35	POLR2A	chr2:86365427-86365466	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr2:86365496-86365514	MCF-7	breast:	n/a	n/a
37	POLR2A	chr2:86364991-86365033	MCF-7	breast:	n/a	n/a
38	POLR2A	chr2:86364779-86369461	GM12892	blood:	n/a	n/a
39	POLR2A	chr2:86366503-86369327	HepG2	liver:	n/a	n/a
40	POLR2A	chr2:86365814-86366096	MCF-7	breast:	n/a	n/a
41	POLR2A	chr2:86364959-86365057	MCF-7	breast:	n/a	n/a
42	POLR2A	chr2:86363795-86364091	HepG2	liver:	n/a	n/a
43	POLR2A	chr2:86365204-86365721	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr2:86365299-86365708	GM12892	blood:	n/a	n/a
45	POLR2A	chr2:86366283-86367087	HL-60	blood:	n/a	n/a
46	POLR2A	chr2:86364885-86365093	GM12878	blood:	n/a	n/a
47	POLR2A	chr2:86365529-86366454	HepG2	liver:	n/a	n/a
48	POLR2A	chr2:86365344-86367265	HepG2	liver:	n/a	n/a
49	POLR2A	chr2:86366325-86369509	K562	blood:	n/a	n/a
50	POLR2A	chr2:86365837-86366113	HL-60	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:86363010-86363060	HL-60	blood:	n/a
2	chr2:86362935-86362985	MCF-7	breast:	n/a
3	chr2:86363010-86363060	AG04449	skin:	fetal
4	chr2:86362935-86362985	H1-hESC	embryonic stem cell:	embryo
5	chr2:86362935-86362985	LNCaP	prostate:	n/a
6	chr2:86363010-86363060	HRPEpiC	eye:	n/a
7	chr2:86362935-86362985	NT2-D1	testis:	n/a
8	chr2:86362935-86362985	RPTEC	kidney:	n/a
9	chr2:86362935-86362985	CMK	blood:	n/a
10	chr2:86363010-86363060	T-47D	breast:	n/a
11	chr2:86362935-86362985	HCPEpiC	choroid plexus:	n/a
12	chr2:86362935-86362985	HUVEC	blood vessel:	n/a
13	chr2:86362935-86362985	PrEC	prostate:	n/a
14	chr2:86363010-86363060	BE2_C	brain:	n/a
15	chr2:86362935-86362985	HCT-116	colon:	n/a
16	chr2:86362935-86362985	GM12891	blood:	n/a
17	chr2:86362935-86362985	ovcar-3	ovarian:	n/a
18	chr2:86363010-86363060	HUVEC	blood vessel:	n/a
19	chr2:86363010-86363060	HepG2	liver:	n/a
20	chr2:86363010-86363060	PANC-1	pancreas:	n/a
21	chr2:86362935-86362985	SK-N-SH	brain:	n/a
22	chr2:86362935-86362985	BE2_C	brain:	n/a
23	chr2:86363010-86363060	NHDF-neo	bronchial:	n/a
24	chr2:86362935-86362985	HRE	kidney:	n/a
25	chr2:86362935-86362985	ECC-1	luminal epithelium:	n/a
26	chr2:86362935-86362985	K562	blood:	n/a
27	chr2:86363010-86363060	HRE	kidney:	n/a
28	chr2:86363010-86363060	AG09309	skin:	n/a
29	chr2:86362935-86362985	GM19239	blood:	n/a
30	chr2:86363010-86363060	GM12892	blood:	n/a
31	chr2:86362935-86362985	HepG2	liver:	n/a
32	chr2:86363010-86363060	NB4	blood:	n/a
33	chr2:86362935-86362985	HEEpiC	esophagus:	n/a
34	chr2:86363010-86363060	AoSMC	blood vessel:	n/a
35	chr2:86362935-86362985	AG04450	lung:	fetal
36	chr2:86363010-86363060	AG10803	skin:	n/a
37	chr2:86363010-86363060	SK-N-MC	brain:	n/a
38	chr2:86363010-86363060	GM12891	blood:	n/a
39	chr2:86363010-86363060	ProgFib	skin:	n/a
40	chr2:86363010-86363060	Jurkat	blood:	n/a
41	chr2:86362935-86362985	Hepatocyte	liver:	n/a
42	chr2:86362935-86362985	ProgFib	skin:	n/a
43	chr2:86362935-86362985	U87	brain:	n/a
44	chr2:86362935-86362985	BJ	skin:	n/a
45	chr2:86362935-86362985	NH-A	brain:	n/a
46	chr2:86363010-86363060	ovcar-3	ovarian:	n/a
47	chr2:86363010-86363060	PFSK-1	brain:	n/a
48	chr2:86363010-86363060	K562	blood:	n/a
49	chr2:86362935-86362985	AG09319	gingival:	n/a
50	chr2:86362935-86362985	PFSK-1	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:86366245..86368824-chr2:86404814..86406615,2	K562	blood:
2	chr2:86353380..86355407-chr2:86359853..86362775,2	MCF-7	breast:
3	chr2:86364997..86367553-chr2:86368696..86371224,3	MCF-7	breast:
4	chr2:86356791..86359394-chr2:86360865..86362824,2	K562	blood:
5	chr2:86358708..86360276-chr2:86362915..86364610,2	K562	blood:
6	chr2:86361107..86363381-chr2:86365316..86368270,4	K562	blood:
7	chr2:86366197..86371549-chr2:86375005..86380562,7	K562	blood:
8	chr2:86358776..86362448-chr2:86362672..86364882,4	K562	blood:
9	chr2:86364964..86367249-chr2:86370579..86373719,3	K562	blood:
10	chr2:86366319..86368824-chr2:86404214..86406615,2	K562	blood:

No data

Variant related genes	Relation type
SNORD94	TF binding region
SNORD94	CpG island
ENSG00000208772	chromatin interactions
ENSG00000132300	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374757207	chr2:86362798-86362799	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181647881	chr2:86362869-86362870	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556682504	chr2:86362898-86362899	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116799667	chr2:86362899-86362900	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542640249	chr2:86362962-86362963	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs367695454	chr2:86362985-86362986	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147801187	chr2:86363006-86363007	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs3770069	chr2:86363074-86363075	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs565482640	chr2:86363081-86363082	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369611868	chr2:86363153-86363154	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532802594	chr2:86363154-86363155	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372355480	chr2:86363168-86363169	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538461423	chr2:86363209-86363210	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544710038	chr2:86363266-86363267	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563006513	chr2:86363321-86363322	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs530022166	chr2:86363352-86363353	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548588474	chr2:86363373-86363374	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs556809099	chr2:86363421-86363422	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567417238	chr2:86363437-86363438	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138989521	chr2:86363447-86363448	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568788603	chr2:86363461-86363462	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546428103	chr2:86363463-86363464	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529360194	chr2:86363502-86363503	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577594752	chr2:86363527-86363528	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112717516	chr2:86363612-86363613	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186292728	chr2:86363616-86363617	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs556620977	chr2:86363619-86363620	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377293394	chr2:86363697-86363698	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192506947	chr2:86363724-86363725	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs375156355	chr2:86363736-86363737	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554564727	chr2:86363752-86363753	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113856008	chr2:86363767-86363768	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573416684	chr2:86363809-86363810	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7558040	chr2:86363855-86363856	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs180824825	chr2:86363925-86363926	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149015534	chr2:86363963-86363964	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145770579	chr2:86364055-86364056	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201721699	chr2:86364076-86364077	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs72839327	chr2:86364115-86364116	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201724046	chr2:86364146-86364147	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201242466	chr2:86364147-86364148	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200786483	chr2:86364182-86364183	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144692694	chr2:86364202-86364203	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541820007	chr2:86364205-86364206	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373005797	chr2:86364225-86364226	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146619705	chr2:86364290-86364291	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2241434	chr2:86364353-86364354	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs540785464	chr2:86364392-86364393	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141293154	chr2:86364408-86364409	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532152379	chr2:86364477-86364478	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	21346763	CNVD
Autism	22495309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86334400-86362800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:86335000-86379000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:86335000-86409000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:86335200-86366600	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr2:86335200-86380800	Strong transcription	Fetal Thymus	thymus
6	chr2:86335400-86394000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:86335400-86408800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:86335600-86366600	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr2:86335600-86366800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr2:86335600-86368000	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr2:86335600-86369200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr2:86335600-86373600	Strong transcription	K562	blood
13	chr2:86335600-86378800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:86335600-86379000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:86335600-86379000	Strong transcription	Duodenum Mucosa	Duodenum
16	chr2:86335600-86379000	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr2:86335600-86394000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr2:86335600-86401000	Strong transcription	Placenta	Placenta
19	chr2:86335600-86407400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr2:86335600-86408600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr2:86335800-86378600	Strong transcription	Fetal Brain Female	brain
22	chr2:86336000-86365800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr2:86336000-86378600	Strong transcription	Brain Germinal Matrix	brain
24	chr2:86336000-86378800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr2:86336000-86378800	Strong transcription	Liver	Liver
26	chr2:86336000-86380800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:86336000-86401200	Strong transcription	Adipose Nuclei	Adipose
28	chr2:86336200-86366600	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr2:86336600-86363000	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr2:86336600-86369400	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr2:86336600-86378600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:86336600-86378600	Strong transcription	Fetal Muscle Leg	muscle
33	chr2:86336600-86378800	Strong transcription	Fetal Intestine Large	intestine
34	chr2:86336600-86378800	Strong transcription	Fetal Muscle Trunk	muscle
35	chr2:86336600-86378800	Strong transcription	Rectal Smooth Muscle	rectum
36	chr2:86336600-86394200	Strong transcription	Primary T cells from cord blood	blood
37	chr2:86336800-86379200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:86336800-86407400	Strong transcription	Dnd41	blood
39	chr2:86337600-86365800	Strong transcription	Thymus	Thymus
40	chr2:86337600-86367800	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr2:86337600-86369400	Strong transcription	Spleen	Spleen
42	chr2:86337600-86378600	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr2:86337600-86378800	Strong transcription	Stomach Smooth Muscle	stomach
44	chr2:86339400-86379000	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr2:86340000-86365800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr2:86340000-86366800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr2:86340800-86368000	Strong transcription	Primary hematopoietic stem cells	blood
48	chr2:86340800-86378800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr2:86341200-86379400	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr2:86341400-86366600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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