Variant report

Variant	esv3357463
Chromosome Location	chr2:10333551-10336049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr2:10334171-10334321	MCF10A-Er-Src	breast:	n/a	chr2:10334239-10334250 chr2:10334241-10334250 chr2:10334241-10334249 chr2:10334240-10334250 chr2:10334242-10334249 chr2:10334240-10334249
2	FOS	chr2:10334112-10334413	HUVEC	blood vessel:	n/a	chr2:10334239-10334250 chr2:10334241-10334250 chr2:10334241-10334249 chr2:10334240-10334250 chr2:10334242-10334249 chr2:10334240-10334249
3	JUND	chr2:10334073-10334407	HepG2	liver:	n/a	chr2:10334241-10334250 chr2:10334241-10334249 chr2:10334239-10334250 chr2:10334240-10334250 chr2:10334242-10334249 chr2:10334240-10334249
4	NFIC	chr2:10334385-10335040	ECC-1	luminal epithelium:	n/a	n/a
5	NFIC	chr2:10334377-10334998	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr2:10334592-10335493	K562	blood:	n/a	n/a
7	POLR2A	chr2:10334122-10334190	HepG2	liver:	n/a	n/a
8	POLR2A	chr2:10334408-10334761	HepG2	liver:	n/a	n/a
9	POLR2A	chr2:10334262-10334501	K562	blood:	n/a	n/a
10	RAD21	chr2:10335946-10337232	SK-N-SH	brain:	n/a	chr2:10336789-10336802 chr2:10336890-10336904
11	TCF12	chr2:10334339-10335180	ECC-1	luminal epithelium:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10334372-10334422	MCF10A-Er-Src	breast:	n/a
2	chr2:10334372-10334422	PANC-1	pancreas:	n/a
3	chr2:10334372-10334422	ovcar-3	ovarian:	n/a
4	chr2:10334372-10334422	NH-A	brain:	n/a
5	chr2:10334372-10334422	Hela-S3	cervix:	n/a
6	chr2:10334372-10334422	BE2_C	brain:	n/a
7	chr2:10334372-10334422	SK-N-SH_RA	brain:	n/a
8	chr2:10334372-10334422	HCPEpiC	choroid plexus:	n/a
9	chr2:10334372-10334422	BJ	skin:	n/a
10	chr2:10334372-10334422	Hepatocyte	liver:	n/a
11	chr2:10334372-10334422	MCF-7	breast:	n/a
12	chr2:10334372-10334422	HRPEpiC	eye:	n/a
13	chr2:10334372-10334422	PrEC	prostate:	n/a
14	chr2:10334372-10334422	RPTEC	kidney:	n/a
15	chr2:10334372-10334422	ECC-1	luminal epithelium:	n/a
16	chr2:10334372-10334422	PFSK-1	brain:	n/a
17	chr2:10334372-10334422	HRE	kidney:	n/a
18	chr2:10334372-10334422	GM12892	blood:	n/a
19	chr2:10334372-10334422	AG09319	gingival:	n/a
20	chr2:10334372-10334422	NHDF-neo	bronchial:	n/a
21	chr2:10334372-10334422	T-47D	breast:	n/a
22	chr2:10334372-10334422	HEEpiC	esophagus:	n/a
23	chr2:10334372-10334422	AoSMC	blood vessel:	n/a
24	chr2:10334372-10334422	AG04450	lung:	fetal
25	chr2:10334372-10334422	HIPEpiC	eye:	n/a
26	chr2:10334372-10334422	NB4	blood:	n/a
27	chr2:10334372-10334422	SAEC	small airway:	n/a
28	chr2:10334372-10334422	GM12891	blood:	n/a
29	chr2:10334372-10334422	SK-N-MC	brain:	n/a
30	chr2:10334372-10334422	U87	brain:	n/a
31	chr2:10334372-10334422	Caco-2	colon:	n/a
32	chr2:10334372-10334422	HCT-116	colon:	n/a
33	chr2:10334372-10334422	Jurkat	blood:	n/a
34	chr2:10334372-10334422	CMK	blood:	n/a
35	chr2:10334372-10334422	ProgFib	skin:	n/a
36	chr2:10334372-10334422	NHBE	bronchial:	n/a
37	chr2:10334372-10334422	GM12878	blood:	n/a
38	chr2:10334372-10334422	GM06990	blood:	n/a
39	chr2:10334372-10334422	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:10334372-10334422	HEK293	kidney:	embryo
41	chr2:10334372-10334422	HNPCEpiC	eye:	n/a
42	chr2:10334372-10334422	NT2-D1	testis:	n/a
43	chr2:10334372-10334422	SKMC	muscle:	n/a
44	chr2:10334372-10334422	H1-hESC	embryonic stem cell:	embryo
45	chr2:10334372-10334422	HAEpiC	amniotic membrane:	n/a
46	chr2:10334372-10334422	HCF	heart:	n/a
47	chr2:10334372-10334422	AG04449	skin:	fetal
48	chr2:10334372-10334422	HRCEpiC	kidney:	n/a
49	chr2:10334372-10334422	LNCaP	prostate:	n/a
50	chr2:10334372-10334422	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:10333815..10336556-chr2:10366578..10368507,2	MCF-7	breast:
2	chr2:10333609..10335207-chr2:10346879..10348820,2	K562	blood:
3	chr2:10272209..10275438-chr2:10333614..10336814,3	K562	blood:
4	chr16:2902125..2904816-chr2:10333422..10334922,2	MCF-7	breast:
5	chr2:10261562..10263628-chr2:10332391..10333942,2	K562	blood:
6	chr2:10276382..10278828-chr2:10333001..10334634,2	MCF-7	breast:
7	chr2:10335310..10337198-chr2:10565374..10566915,2	K562	blood:
8	chr2:10260909..10263628-chr2:10332391..10334618,3	K562	blood:

No data

Variant related genes	Relation type
MIR4261	TF binding region
MIR4261	CpG island
ENSG00000171848	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369671500	chr2:10333556-10333557	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs147441759	chr2:10333578-10333579	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563038294	chr2:10333599-10333600	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530215582	chr2:10333609-10333610	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75560159	chr2:10333635-10333636	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531389684	chr2:10333655-10333656	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148507072	chr2:10333656-10333657	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375018828	chr2:10333660-10333661	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568234482	chr2:10333661-10333662	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189478714	chr2:10333662-10333663	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs13407907	chr2:10333746-10333747	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546145944	chr2:10333754-10333755	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs180767490	chr2:10333764-10333765	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs13383316	chr2:10333767-10333768	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556767748	chr2:10333768-10333769	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568964234	chr2:10333847-10333848	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141858074	chr2:10333866-10333867	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554819362	chr2:10333961-10333962	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186336612	chr2:10333978-10333979	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540535789	chr2:10333993-10333994	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558937991	chr2:10333994-10333995	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577300338	chr2:10333997-10333998	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150619143	chr2:10334015-10334016	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139749307	chr2:10334035-10334036	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574895418	chr2:10334075-10334076	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs60537578	chr2:10334095-10334096	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576743561	chr2:10334128-10334129	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs536031217	chr2:10334130-10334131	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111457788	chr2:10334137-10334138	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs72788356	chr2:10334148-10334149	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552444629	chr2:10334197-10334198	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75276028	chr2:10334249-10334250	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531992536	chr2:10334289-10334290	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114385757	chr2:10334322-10334323	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs146835547	chr2:10334350-10334351	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114615043	chr2:10334362-10334363	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548358713	chr2:10334372-10334373	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190833769	chr2:10334418-10334419	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116037324	chr2:10334420-10334421	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558875543	chr2:10334426-10334427	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs139728329	chr2:10334475-10334476	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113800122	chr2:10334497-10334498	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556533666	chr2:10334505-10334506	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs144507193	chr2:10334538-10334539	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145424023	chr2:10334553-10334554	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560256330	chr2:10334555-10334556	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572292193	chr2:10334565-10334566	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138402140	chr2:10334584-10334585	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201427958	chr2:10334609-10334610	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546018738	chr2:10334646-10334647	Enhancers Weak transcription Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10290200-10351400	Strong transcription	Dnd41	blood
2	chr2:10302400-10337600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:10304400-10339800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:10311800-10337000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:10313000-10344400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:10314000-10340400	Weak transcription	HepG2	liver
7	chr2:10320600-10337200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:10320800-10336800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:10321800-10338000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:10325600-10342800	Weak transcription	Fetal Brain Female	brain
11	chr2:10326600-10339400	Strong transcription	Thymus	Thymus
12	chr2:10327600-10333600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr2:10328200-10336600	Weak transcription	Brain Germinal Matrix	brain
14	chr2:10328800-10336600	Weak transcription	Gastric	stomach
15	chr2:10329000-10337200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr2:10329800-10333600	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr2:10330800-10334000	Weak transcription	Fetal Kidney	kidney
18	chr2:10331800-10333600	Weak transcription	Fetal Thymus	thymus
19	chr2:10331800-10333800	Weak transcription	Spleen	Spleen
20	chr2:10332000-10333800	Weak transcription	Esophagus	oesophagus
21	chr2:10332000-10337400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr2:10332200-10334400	Weak transcription	Fetal Intestine Small	intestine
23	chr2:10332400-10335200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:10332600-10333600	Weak transcription	Right Ventricle	heart
25	chr2:10332600-10334600	Enhancers	Fetal Muscle Leg	muscle
26	chr2:10332800-10333800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr2:10333000-10334600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:10333000-10334600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:10333000-10334800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:10333000-10335200	Enhancers	Fetal Lung	lung
31	chr2:10333000-10347000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:10333200-10333600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:10333200-10334600	Enhancers	NHLF	lung
34	chr2:10333200-10334600	Enhancers	Osteobl	bone
35	chr2:10333200-10334800	Enhancers	NHDF-Ad	bronchial
36	chr2:10333400-10333600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr2:10333400-10334200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr2:10333400-10334800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:10333400-10334800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr2:10333400-10335000	Enhancers	Fetal Stomach	stomach
41	chr2:10333400-10335200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:10333600-10333800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:10333600-10333800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr2:10333600-10333800	Enhancers	Right Ventricle	heart
45	chr2:10333600-10333800	Enhancers	Stomach Mucosa	stomach
46	chr2:10333600-10334000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr2:10333600-10334400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:10333600-10334400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr2:10333600-10334600	Enhancers	Placenta	Placenta
50	chr2:10333600-10335200	Strong transcription	Monocytes-CD14+_RO01746	blood

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