Variant report

Variant	nsv471643
Chromosome Location	chr7:102203036-102359973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4695)
CpG islands
(count:1037)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4695 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102212897-102213097	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
3	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
4	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
5	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
6	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
7	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
8	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
9	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
10	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:102214079-102214404	GM12878	blood:	n/a	n/a
12	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
13	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
14	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
15	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
16	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
17	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
18	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
19	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
20	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
21	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
22	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
23	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
24	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
25	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
26	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
27	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
28	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a
29	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
30	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
31	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
32	BATF	chr7:102212379-102213628	GM12878	blood:	n/a	n/a
33	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
34	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
35	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
36	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
37	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
38	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
39	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
40	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
41	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
42	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
43	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
44	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
45	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
46	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a
47	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
48	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
49	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
50	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102312308-102312358	HAEpiC	amniotic membrane:	n/a
2	chr7:102212892-102212942	PFSK-1	brain:	n/a
3	chr7:102312315-102312365	GM06990	blood:	n/a
4	chr7:102313389-102313439	ovcar-3	ovarian:	n/a
5	chr7:102312315-102312365	IMR90	lung:	fetal
6	chr7:102308061-102308111	AoSMC	blood vessel:	n/a
7	chr7:102212892-102212942	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:102327236-102327286	AG04450	lung:	fetal
9	chr7:102246378-102246428	PFSK-1	brain:	n/a
10	chr7:102332458-102332508	Caco-2	colon:	n/a
11	chr7:102312200-102312250	AG10803	skin:	n/a
12	chr7:102312318-102312368	PrEC	prostate:	n/a
13	chr7:102327236-102327286	A549	lung:	n/a
14	chr7:102259241-102259291	MCF10A-Er-Src	breast:	n/a
15	chr7:102246378-102246428	HRE	kidney:	n/a
16	chr7:102311965-102312015	Hela-S3	cervix:	n/a
17	chr7:102259241-102259291	IMR90	lung:	fetal
18	chr7:102212892-102212942	SK-N-SH	brain:	n/a
19	chr7:102312331-102312381	ovcar-3	ovarian:	n/a
20	chr7:102308061-102308111	HRCEpiC	kidney:	n/a
21	chr7:102259241-102259291	HEEpiC	esophagus:	n/a
22	chr7:102312315-102312365	BJ	skin:	n/a
23	chr7:102311965-102312015	HCT-116	colon:	n/a
24	chr7:102279588-102279638	AG09309	skin:	n/a
25	chr7:102259241-102259291	NB4	blood:	n/a
26	chr7:102312331-102312381	AoSMC	blood vessel:	n/a
27	chr7:102330635-102330685	A549	lung:	n/a
28	chr7:102330635-102330685	HL-60	blood:	n/a
29	chr7:102312315-102312365	HL-60	blood:	n/a
30	chr7:102311965-102312015	SK-N-MC	brain:	n/a
31	chr7:102246378-102246428	Caco-2	colon:	n/a
32	chr7:102312331-102312381	HCT-116	colon:	n/a
33	chr7:102312308-102312358	MCF-7	breast:	n/a
34	chr7:102212892-102212942	SKMC	muscle:	n/a
35	chr7:102330635-102330685	HAEpiC	amniotic membrane:	n/a
36	chr7:102329146-102329196	ProgFib	skin:	n/a
37	chr7:102279588-102279638	PANC-1	pancreas:	n/a
38	chr7:102329146-102329196	Jurkat	blood:	n/a
39	chr7:102327236-102327286	HRPEpiC	eye:	n/a
40	chr7:102259241-102259291	HCT-116	colon:	n/a
41	chr7:102246378-102246428	BJ	skin:	n/a
42	chr7:102327236-102327286	NB4	blood:	n/a
43	chr7:102259241-102259291	BJ	skin:	n/a
44	chr7:102308061-102308111	NH-A	brain:	n/a
45	chr7:102327236-102327286	HAEpiC	amniotic membrane:	n/a
46	chr7:102329146-102329196	AG04450	lung:	fetal
47	chr7:102279588-102279638	SAEC	small airway:	n/a
48	chr7:102312308-102312358	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:102311965-102312015	GM12892	blood:	n/a
50	chr7:102329146-102329196	NHBE	bronchial:	n/a

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RASA4	hsa-miR-335-5p	chr7:102227581-102227605

Variant related genes	Relation type
ENSG00000270249	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
ENSG00000205236	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
POLR2J3	TF binding region
SPDYE2B	TF binding region
ENSG00000270249	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
ENSG00000205236	CpG island
RASA4	CpG island
RASA4DP	CpG island
POLR2J3	CpG island
SPDYE2B	CpG island

Extended variants
information (count: 1810 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1810 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376757044	chr7:102204226-102204227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371323533	chr7:102204259-102204260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112830398	chr7:102204427-102204428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202014335	chr7:102204545-102204546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533957747	chr7:102204559-102204560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555323739	chr7:102204608-102204609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs29001468	chr7:102204633-102204634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573413749	chr7:102204692-102204693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28445991	chr7:102204697-102204698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567876933	chr7:102204826-102204827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200969709	chr7:102204862-102204863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373090622	chr7:102204910-102204911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538500337	chr7:102204927-102204928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376077571	chr7:102204986-102204987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556483831	chr7:102205008-102205009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201898488	chr7:102205145-102205146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374993693	chr7:102205146-102205147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200366507	chr7:102205153-102205154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578092164	chr7:102205155-102205156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370354243	chr7:102205169-102205170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545261885	chr7:102205231-102205232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553954693	chr7:102205302-102205303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373798940	chr7:102205378-102205379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367559153	chr7:102205417-102205418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572157363	chr7:102205523-102205524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62482995	chr7:102205575-102205576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542661454	chr7:102205644-102205645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560840306	chr7:102205779-102205780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531511786	chr7:102206080-102206081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543664899	chr7:102206083-102206084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371129501	chr7:102206091-102206092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201172473	chr7:102206171-102206172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112986176	chr7:102206176-102206177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368841181	chr7:102206178-102206179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62482996	chr7:102206317-102206318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182739950	chr7:102206324-102206325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146210736	chr7:102206371-102206372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370499903	chr7:102206417-102206418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372551104	chr7:102206418-102206419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376516603	chr7:102206421-102206422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62482997	chr7:102206437-102206438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72494476	chr7:102206443-102206444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368645781	chr7:102206467-102206468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200820296	chr7:102206514-102206515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565027311	chr7:102206663-102206664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532385626	chr7:102206666-102206667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547165582	chr7:102206678-102206679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370502383	chr7:102206719-102206720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527742956	chr7:102206762-102206763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368036596	chr7:102206892-102206893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102168600-102212600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:102173600-102212600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:102174800-102212600	Weak transcription	Fetal Stomach	stomach
4	chr7:102200600-102212600	Weak transcription	Fetal Brain Female	brain
5	chr7:102203000-102212600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:102203600-102212600	Weak transcription	Lung	lung
7	chr7:102203800-102212600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:102203800-102212600	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr7:102203800-102212600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:102204600-102206200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr7:102204800-102212600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:102204800-102212600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:102204800-102212600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:102204800-102212600	Weak transcription	Spleen	Spleen
15	chr7:102205000-102212600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr7:102205000-102212600	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:102205000-102212600	Weak transcription	Brain Germinal Matrix	brain
18	chr7:102205000-102212600	Weak transcription	Left Ventricle	heart
19	chr7:102205600-102212600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:102205600-102212600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:102205600-102212600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:102205600-102212600	Weak transcription	Placenta	Placenta
23	chr7:102206200-102207400	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:102206200-102209800	Weak transcription	Fetal Muscle Leg	muscle
25	chr7:102206200-102212600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:102206200-102212600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:102206200-102212600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:102206200-102212600	Weak transcription	Adipose Nuclei	Adipose
29	chr7:102206200-102212600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr7:102206200-102212600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr7:102206200-102212600	Weak transcription	Fetal Thymus	thymus
32	chr7:102206200-102212600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:102206200-102212600	Weak transcription	Thymus	Thymus
34	chr7:102206800-102212600	Weak transcription	Brain Angular Gyrus	brain
35	chr7:102206800-102212600	Weak transcription	Brain Hippocampus Middle	brain
36	chr7:102207200-102212600	Weak transcription	Primary B cells from cord blood	blood
37	chr7:102207400-102211000	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:102207400-102212600	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr7:102207600-102209800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr7:102209200-102209400	Enhancers	NH-A	brain
41	chr7:102209400-102212600	Weak transcription	NH-A	brain
42	chr7:102209800-102210200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr7:102209800-102210200	Strong transcription	Fetal Muscle Leg	muscle
44	chr7:102210000-102212600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr7:102210000-102212600	Weak transcription	Colon Smooth Muscle	Colon
46	chr7:102210000-102212600	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr7:102210200-102212600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr7:102210200-102212600	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:102211000-102211200	Enhancers	Dnd41	blood
50	chr7:102211000-102211400	Enhancers	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links