Variant report

Variant	esv2761614
Chromosome Location	chr10:93960695-93981177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 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	ARID3A	chr10:93964171-93964249	HepG2	liver:	n/a	n/a
2	ATF1	chr10:93960569-93960760	K562	blood:	n/a	n/a
3	ATF2	chr10:93970909-93971451	GM12878	blood:	n/a	n/a
4	ATF2	chr10:93970898-93971462	GM12878	blood:	n/a	n/a
5	BATF	chr10:93970990-93971355	GM12878	blood:	n/a	chr10:93971193-93971204 chr10:93971194-93971204
6	BATF	chr10:93971080-93971348	GM12878	blood:	n/a	chr10:93971193-93971204 chr10:93971194-93971204
7	BCL11A	chr10:93971038-93971406	GM12878	blood:	n/a	chr10:93971151-93971160
8	BCL11A	chr10:93971033-93971332	GM12878	blood:	n/a	chr10:93971151-93971160
9	BCLAF1	chr10:93970911-93971457	GM12878	blood:	n/a	chr10:93971151-93971160
10	BHLHE40	chr10:93978367-93978595	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:93970994-93971465	GM12878	blood:	n/a	n/a
12	CBX3	chr10:93970883-93971366	HCT-116	colon:	n/a	n/a
13	CCNT2	chr10:93960467-93960754	K562	blood:	n/a	n/a
14	CEBPB	chr10:93978906-93979806	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:93970941-93971342	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr10:93970829-93971504	HCT-116	colon:	n/a	n/a
17	CEBPB	chr10:93976501-93976693	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr10:93979294-93979707	HCT-116	colon:	n/a	n/a
19	CHD2	chr10:93976461-93976667	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr10:93978499-93978574	GM12878	blood:	n/a	n/a
21	CHD2	chr10:93971047-93971349	GM12878	blood:	n/a	n/a
22	CREB1	chr10:93970955-93971479	GM12878	blood:	n/a	n/a
23	CREB1	chr10:93970968-93971361	GM12878	blood:	n/a	n/a
24	CTCF	chr10:93976440-93976590	HEEpiC	esophagus:	n/a	chr10:93976571-93976584
25	CTCF	chr10:93976406-93976705	MCF-7	breast:	n/a	chr10:93976571-93976584
26	CTCF	chr10:93976420-93976570	GM12867	blood:	n/a	n/a
27	CTCF	chr10:93976331-93976744	H1-hESC	embryonic stem cell:	n/a	chr10:93976571-93976584
28	CTCF	chr10:93976540-93976690	GM06990	blood:	n/a	chr10:93976571-93976584
29	CTCF	chr10:93976500-93976650	GM12868	blood:	n/a	chr10:93976571-93976584
30	CTCF	chr10:93976460-93976610	SK-N-SH_RA	brain:	n/a	chr10:93976571-93976584
31	CTCF	chr10:93976400-93976550	GM12873	blood:	n/a	n/a
32	CTCF	chr10:93976465-93976639	GM19238	blood:	n/a	chr10:93976571-93976584
33	CTCF	chr10:93976467-93976593	GM10248	blood:	n/a	chr10:93976571-93976584
34	CTCF	chr10:93976400-93976550	GM12870	blood:	n/a	n/a
35	CTCF	chr10:93976360-93976731	H1-hESC	embryonic stem cell:	n/a	chr10:93976571-93976584
36	CTCF	chr10:93976460-93976610	WERI-Rb-1	eye:	n/a	chr10:93976571-93976584
37	CTCF	chr10:93976420-93976570	NB4	blood:	n/a	n/a
38	CTCF	chr10:93976440-93976590	HEK293	kidney:	n/a	chr10:93976571-93976584
39	CTCF	chr10:93976440-93976590	GM12878	blood:	n/a	chr10:93976571-93976584
40	CTCF	chr10:93976460-93976610	Hela-S3	cervix:	n/a	chr10:93976571-93976584
41	CTCF	chr10:93976400-93976550	GM12872	blood:	n/a	n/a
42	CTCF	chr10:93976427-93976625	A549	lung:	n/a	chr10:93976571-93976584
43	CTCF	chr10:93976450-93976662	Hela-S3	cervix:	n/a	chr10:93976571-93976584
44	CTCF	chr10:93976440-93976590	GM12873	blood:	n/a	chr10:93976571-93976584
45	CTCF	chr10:93976460-93976610	K562	blood:	n/a	chr10:93976571-93976584
46	CTCF	chr10:93964160-93964310	Caco-2	colon:	n/a	n/a
47	CTCF	chr10:93976401-93976706	K562	blood:	n/a	chr10:93976571-93976584
48	CTCF	chr10:93976440-93976590	HUVEC	blood vessel:	n/a	chr10:93976571-93976584
49	CTCF	chr10:93976440-93976590	WERI-Rb-1	eye:	n/a	chr10:93976571-93976584
50	CTCF	chr10:93976520-93976670	GM12873	blood:	n/a	chr10:93976571-93976584

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:93976192-93976242	MCF10A-Er-Src	breast:	n/a
2	chr10:93976192-93976242	AG09309	skin:	n/a
3	chr10:93976249-93976299	HCPEpiC	choroid plexus:	n/a
4	chr10:93976087-93976137	GM12878	blood:	n/a
5	chr10:93976087-93976137	ECC-1	luminal epithelium:	n/a
6	chr10:93976087-93976137	Hepatocyte	liver:	n/a
7	chr10:93976249-93976299	Caco-2	colon:	n/a
8	chr10:93976192-93976242	SAEC	small airway:	n/a
9	chr10:93976192-93976242	HNPCEpiC	eye:	n/a
10	chr10:93976087-93976137	NHDF-neo	bronchial:	n/a
11	chr10:93976192-93976242	AG09319	gingival:	n/a
12	chr10:93976087-93976137	BE2_C	brain:	n/a
13	chr10:93976087-93976137	HCM	heart:	n/a
14	chr10:93976192-93976242	HEK293	kidney:	embryo
15	chr10:93976087-93976137	HAEpiC	amniotic membrane:	n/a
16	chr10:93976249-93976299	PFSK-1	brain:	n/a
17	chr10:93976192-93976242	ECC-1	luminal epithelium:	n/a
18	chr10:93976087-93976137	SK-N-SH_RA	brain:	n/a
19	chr10:93976087-93976137	NB4	blood:	n/a
20	chr10:93976249-93976299	PrEC	prostate:	n/a
21	chr10:93976087-93976137	HRCEpiC	kidney:	n/a
22	chr10:93976087-93976137	A549	lung:	n/a
23	chr10:93976087-93976137	HCPEpiC	choroid plexus:	n/a
24	chr10:93976249-93976299	U87	brain:	n/a
25	chr10:93976249-93976299	NH-A	brain:	n/a
26	chr10:93976192-93976242	IMR90	lung:	fetal
27	chr10:93976192-93976242	HCT-116	colon:	n/a
28	chr10:93976249-93976299	GM12892	blood:	n/a
29	chr10:93976192-93976242	HMEC	breast:	n/a
30	chr10:93976087-93976137	Hela-S3	cervix:	n/a
31	chr10:93976087-93976137	LNCaP	prostate:	n/a
32	chr10:93976087-93976137	HepG2	liver:	n/a
33	chr10:93976249-93976299	HRCEpiC	kidney:	n/a
34	chr10:93976087-93976137	AG10803	skin:	n/a
35	chr10:93976192-93976242	ProgFib	skin:	n/a
36	chr10:93976192-93976242	ovcar-3	ovarian:	n/a
37	chr10:93976192-93976242	HAEpiC	amniotic membrane:	n/a
38	chr10:93976249-93976299	LNCaP	prostate:	n/a
39	chr10:93976249-93976299	IMR90	lung:	fetal
40	chr10:93976249-93976299	AG09319	gingival:	n/a
41	chr10:93976087-93976137	K562	blood:	n/a
42	chr10:93976087-93976137	IMR90	lung:	fetal
43	chr10:93976249-93976299	HRE	kidney:	n/a
44	chr10:93976192-93976242	RPTEC	kidney:	n/a
45	chr10:93976192-93976242	Hepatocyte	liver:	n/a
46	chr10:93976087-93976137	GM19239	blood:	n/a
47	chr10:93976087-93976137	HPAEpiC	pulmonary alveolar:	n/a
48	chr10:93976192-93976242	SKMC	muscle:	n/a
49	chr10:93976087-93976137	GM12891	blood:	n/a
50	chr10:93976249-93976299	Hepatocyte	liver:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:93976217..93977889-chr10:94051487..94052996,2	MCF-7	breast:
2	chr10:93976925..93978749-chr10:94049775..94052495,2	MCF-7	breast:
3	chr10:93958713..93960977-chr10:93966306..93968107,2	MCF-7	breast:
4	chr10:93847286..93847823-chr10:93976420..93976923,2	MCF-7	breast:
5	chr10:93973011..93976411-chr10:94049477..94051967,3	K562	blood:
6	chr10:93958713..93960977-chr10:93966306..93968107,2	MCF-7	breast:
7	chr10:93967344..93971211-chr10:94049163..94052466,3	MCF-7	breast:
8	chr10:93969866..93972797-chr10:93997351..93999951,2	MCF-7	breast:

No data

Variant related genes	Relation type
NHP2P1	TF binding region
ENSG00000221042	TF binding region
NHP2P1	CpG island
ENSG00000221042	CpG island
ENSG00000198060	chromatin interactions
ENSG00000107864	chromatin interactions

Extended variants
information (count: 686 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55937822	chr10:93960734-93960735	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549782508	chr10:93960755-93960756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181349772	chr10:93960766-93960767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185908732	chr10:93960790-93960791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551702753	chr10:93960860-93960861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571348302	chr10:93960920-93960921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189108169	chr10:93960929-93960930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546258126	chr10:93961024-93961025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146842483	chr10:93961051-93961052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200783020	chr10:93961059-93961060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573353658	chr10:93961087-93961088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181727070	chr10:93961106-93961107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545709852	chr10:93961130-93961131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565610308	chr10:93961141-93961142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572507328	chr10:93961195-93961196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74444802	chr10:93961256-93961257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561196109	chr10:93961276-93961277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530147859	chr10:93961286-93961287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs386372087	chr10:93961294-93961295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs58056642	chr10:93961313-93961314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187168717	chr10:93961331-93961332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117962493	chr10:93961353-93961354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192409121	chr10:93961382-93961383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140303854	chr10:93961401-93961402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551345683	chr10:93961402-93961403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571525123	chr10:93961463-93961464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11186851	chr10:93961517-93961518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs74149389	chr10:93961605-93961606	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs145344194	chr10:93961663-93961664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531086692	chr10:93961709-93961710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182508693	chr10:93961714-93961715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576095329	chr10:93961731-93961732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538635247	chr10:93961738-93961739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371453020	chr10:93961786-93961787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558938802	chr10:93961881-93961882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544488154	chr10:93961929-93961930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186139509	chr10:93961941-93961942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191059774	chr10:93961987-93961988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561591137	chr10:93961990-93961991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572719230	chr10:93961991-93961992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146436371	chr10:93962070-93962071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541230368	chr10:93962077-93962078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554725806	chr10:93962097-93962098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11186852	chr10:93962124-93962125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs182527469	chr10:93962313-93962314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187174150	chr10:93962329-93962330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs36005556	chr10:93962343-93962344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78598563	chr10:93962390-93962391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532326058	chr10:93962400-93962401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192091595	chr10:93962425-93962426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93926400-93976000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:93926600-93976000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr10:93926800-93982400	Weak transcription	HSMMtube	muscle
4	chr10:93927000-93963800	Weak transcription	Brain Angular Gyrus	brain
5	chr10:93927000-93966200	Weak transcription	Ovary	ovary
6	chr10:93927000-93970800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr10:93927200-93967600	Weak transcription	Adipose Nuclei	Adipose
8	chr10:93927200-93980400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr10:93927400-93966600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:93927400-93970800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr10:93927400-93997800	Weak transcription	Fetal Intestine Large	intestine
12	chr10:93929200-93984800	Weak transcription	Fetal Intestine Small	intestine
13	chr10:93929400-93967800	Weak transcription	Colon Smooth Muscle	Colon
14	chr10:93934200-93976200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:93940200-93971200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr10:93940600-93970800	Weak transcription	Fetal Stomach	stomach
17	chr10:93941800-93968000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr10:93941800-93971200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr10:93945800-93963800	Weak transcription	Fetal Brain Female	brain
20	chr10:93946600-93964000	Weak transcription	Left Ventricle	heart
21	chr10:93947800-93967800	Weak transcription	GM12878-XiMat	blood
22	chr10:93949000-93961800	Weak transcription	Primary T cells from cord blood	blood
23	chr10:93952400-93963400	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr10:93952600-93966200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr10:93956200-93967000	Weak transcription	Fetal Heart	heart
26	chr10:93958200-93968400	Weak transcription	Right Atrium	heart
27	chr10:93958400-93963800	Weak transcription	Right Ventricle	heart
28	chr10:93958400-93967600	Weak transcription	Brain Anterior Caudate	brain
29	chr10:93958400-93981000	Weak transcription	Psoas Muscle	Psoas
30	chr10:93958600-93961200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr10:93958800-93962800	Weak transcription	Aorta	Aorta
32	chr10:93958800-93967000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr10:93958800-93967000	Weak transcription	Brain Hippocampus Middle	brain
34	chr10:93959000-93969800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr10:93959000-93985800	Weak transcription	Brain Substantia Nigra	brain
36	chr10:93960000-93960800	Enhancers	HUVEC	blood vessel
37	chr10:93960000-93961200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr10:93960400-93960800	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr10:93960400-93960800	Enhancers	Hela-S3	cervix
40	chr10:93960400-93960800	Enhancers	K562	blood
41	chr10:93960600-93960800	Enhancers	Gastric	stomach
42	chr10:93960600-93961000	Enhancers	NHEK	skin
43	chr10:93960600-93961400	Enhancers	HMEC	breast
44	chr10:93960600-93961600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:93960600-93962000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr10:93960800-93967000	Weak transcription	K562	blood
47	chr10:93960800-93970000	Weak transcription	Hela-S3	cervix
48	chr10:93960800-93970800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr10:93960800-93976000	Weak transcription	Gastric	stomach
50	chr10:93961000-93990800	Weak transcription	Spleen	Spleen

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