Variant report

Variant	esv1797969
Chromosome Location	chr7:102394076-102399857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:102398676-102398970	K562	blood:	n/a	n/a
2	CTCF	chr7:102398840-102398990	NHDF-neo	bronchial:	n/a	n/a
3	CTCF	chr7:102398713-102398900	GM10266	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
4	CTCF	chr7:102398820-102398970	HCM	heart:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
5	CTCF	chr7:102398820-102398970	HA-sp	spinal cord:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
6	CTCF	chr7:102398780-102398930	GM12878	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
7	CTCF	chr7:102398840-102398990	HVMF	connective:	n/a	n/a
8	CTCF	chr7:102398780-102398930	GM06990	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
9	CTCF	chr7:102398713-102398933	Kidney_OC	kidney:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
10	CTCF	chr7:102398682-102398976	Medullo	brain:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
11	CTCF	chr7:102398800-102398950	AG10803	skin:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
12	CTCF	chr7:102398800-102398950	BJ	skin:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
13	CTCF	chr7:102398820-102398970	SK-N-SH_RA	brain:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
14	CTCF	chr7:102398560-102398710	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr7:102398840-102398990	NHLF	lung:	n/a	n/a
16	CTCF	chr7:102398840-102398990	HCM	heart:	n/a	n/a
17	CTCF	chr7:102398800-102398950	HEEpiC	esophagus:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
18	CTCF	chr7:102398820-102398970	NB4	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
19	CTCF	chr7:102398780-102398930	HCPEpiC	choroid plexus:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
20	CTCF	chr7:102398540-102398690	AG10803	skin:	n/a	n/a
21	CTCF	chr7:102398726-102398870	MCF-7	breast:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
22	CTCF	chr7:102398820-102398970	HFF-Myc	foreskin:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
23	CTCF	chr7:102398710-102398875	GM12878	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
24	CTCF	chr7:102398673-102398956	K562	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
25	CTCF	chr7:102398714-102398928	A549	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
26	CTCF	chr7:102398760-102398910	GM06990	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
27	CTCF	chr7:102398702-102398922	K562	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
28	CTCF	chr7:102398670-102398965	IMR90	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
29	CTCF	chr7:102398800-102398950	GM12873	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
30	CTCF	chr7:102398800-102398950	HPF	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
31	CTCF	chr7:102398800-102398950	HRE	kidney:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
32	CTCF	chr7:102398637-102398975	K562	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
33	CTCF	chr7:102398800-102398950	HMF	breast:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
34	CTCF	chr7:102398840-102398990	GM12873	blood:	n/a	n/a
35	CTCF	chr7:102398677-102398994	Spleen_OC	spleen:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
36	CTCF	chr7:102398770-102398967	MCF-7	breast:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
37	CTCF	chr7:102398800-102398950	AG09319	gingival:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
38	CTCF	chr7:102398800-102398950	HRPEpiC	eye:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
39	CTCF	chr7:102398820-102398970	WI-38	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
40	CTCF	chr7:102398645-102399110	A549	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
41	CTCF	chr7:102398567-102399019	A549	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
42	CTCF	chr7:102398719-102398925	LNCaP	prostate:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
43	CTCF	chr7:102398800-102398950	HCFaa	heart:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
44	CTCF	chr7:102398560-102398710	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr7:102398840-102398990	AG04450	lung:	n/a	n/a
46	CTCF	chr7:102398781-102398877	GM20000	blood:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
47	CTCF	chr7:102398800-102398950	AG04450	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
48	CTCF	chr7:102398691-102399027	A549	lung:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
49	CTCF	chr7:102398724-102398938	Pancreas_OC	pancreas:	n/a	chr7:102398831-102398847 chr7:102398833-102398846 chr7:102398832-102398853 chr7:102398830-102398848
50	CTCF	chr7:102398840-102398990	GM12872	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:102396782..102398459-chr7:102714684..102716364,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000213385	TF binding region
ENSG00000170632	chromatin interactions
ENSG00000161040	chromatin interactions

Extended variants
information (count: 193 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:193 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10226473	chr7:102394076-102394077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181075123	chr7:102394085-102394086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536480694	chr7:102394145-102394146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551321147	chr7:102394188-102394189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200419270	chr7:102394189-102394190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554802987	chr7:102394238-102394239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2539367	chr7:102394286-102394287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574227972	chr7:102394328-102394329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2539366	chr7:102394358-102394359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs2537466	chr7:102394415-102394416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs577931620	chr7:102394422-102394423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2539365	chr7:102394424-102394425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545699900	chr7:102394447-102394448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560649719	chr7:102394458-102394459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28632028	chr7:102394532-102394533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527983114	chr7:102394544-102394545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549205686	chr7:102394557-102394558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28514781	chr7:102394596-102394597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74300427	chr7:102394627-102394628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75491830	chr7:102394642-102394643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201375958	chr7:102394652-102394653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75687357	chr7:102394663-102394664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78927565	chr7:102394664-102394665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12113669	chr7:102394671-102394672	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2539363	chr7:102394772-102394773	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs28542122	chr7:102394797-102394798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28676980	chr7:102394799-102394800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549436115	chr7:102394803-102394804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28420779	chr7:102394824-102394825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28397762	chr7:102394869-102394870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571234274	chr7:102394891-102394892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538288129	chr7:102394917-102394918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71296537	chr7:102394918-102394919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28666505	chr7:102394924-102394925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547350733	chr7:102394931-102394932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2537465	chr7:102394984-102394985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565884533	chr7:102395005-102395006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536543239	chr7:102395007-102395008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200221544	chr7:102395040-102395041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113400963	chr7:102395051-102395052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374206426	chr7:102395052-102395053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576259542	chr7:102395056-102395057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367990529	chr7:102395072-102395073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112320093	chr7:102395086-102395087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147563877	chr7:102395087-102395088	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75841291	chr7:102395185-102395186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2537464	chr7:102395236-102395237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28664649	chr7:102395243-102395244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545118851	chr7:102395264-102395265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183719245	chr7:102395290-102395291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102390000-102394600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:102390000-102396400	Weak transcription	Spleen	Spleen
3	chr7:102390000-102402000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:102390000-102404000	Weak transcription	Aorta	Aorta
5	chr7:102390000-102405000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:102390000-102405200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:102390000-102421000	Weak transcription	Lung	lung
8	chr7:102390000-102434400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:102390200-102397600	Weak transcription	Placenta	Placenta
10	chr7:102390200-102397800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:102390200-102401200	Weak transcription	Gastric	stomach
12	chr7:102390200-102419200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:102390200-102432000	Weak transcription	Left Ventricle	heart
14	chr7:102390400-102411400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr7:102390400-102421000	Weak transcription	Fetal Intestine Large	intestine
16	chr7:102390400-102421200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr7:102390600-102396200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:102390600-102396400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:102390600-102402000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:102390600-102404000	Weak transcription	Pancreas	Pancrea
21	chr7:102390600-102404200	Weak transcription	Ovary	ovary
22	chr7:102390600-102405400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:102390600-102406400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr7:102390600-102420400	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr7:102390600-102421000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:102390600-102421000	Weak transcription	Thymus	Thymus
27	chr7:102390600-102421200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr7:102390600-102422600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr7:102390800-102394600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:102390800-102394600	Weak transcription	Fetal Stomach	stomach
31	chr7:102390800-102394600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr7:102390800-102396800	Weak transcription	Osteobl	bone
33	chr7:102390800-102397800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:102390800-102397800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:102390800-102397800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr7:102390800-102398200	Weak transcription	HMEC	breast
37	chr7:102390800-102398600	Weak transcription	Brain Hippocampus Middle	brain
38	chr7:102390800-102402200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr7:102390800-102403600	Weak transcription	Fetal Heart	heart
40	chr7:102390800-102404000	Weak transcription	Fetal Lung	lung
41	chr7:102390800-102405000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr7:102390800-102406800	Weak transcription	Brain Anterior Caudate	brain
43	chr7:102390800-102421200	Weak transcription	Brain Germinal Matrix	brain
44	chr7:102390800-102421200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr7:102390800-102448800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:102391000-102394600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:102391000-102394600	Weak transcription	Fetal Intestine Small	intestine
48	chr7:102391000-102398000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr7:102391000-102398000	Weak transcription	A549	lung
50	chr7:102391000-102402000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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