Variant report

Variant	esv1800315
Chromosome Location	chr3:69374729-69414587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:69375893-69376474	GM12878	blood:	n/a	n/a
2	ATF2	chr3:69375857-69376503	GM12878	blood:	n/a	n/a
3	BATF	chr3:69402729-69403057	GM12878	blood:	n/a	n/a
4	BATF	chr3:69375943-69376426	GM12878	blood:	n/a	n/a
5	BATF	chr3:69402806-69403041	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:69376078-69376357	GM12878	blood:	n/a	chr3:69376225-69376234
7	BCL3	chr3:69388494-69388847	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:69375830-69376535	GM12878	blood:	n/a	chr3:69376225-69376234
9	BHLHE40	chr3:69377529-69377687	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:69402548-69403163	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:69375893-69376556	GM12878	blood:	n/a	n/a
12	BRCA1	chr3:69403990-69404034	GM12878	blood:	n/a	n/a
13	CEBPB	chr3:69406405-69406753	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:69412148-69412487	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:69412156-69412463	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:69412187-69412411	A549	lung:	n/a	n/a
17	CEBPB	chr3:69402946-69403150	HepG2	liver:	n/a	chr3:69403048-69403061
18	CEBPB	chr3:69412159-69412382	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:69413433-69413807	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:69389915-69390115	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:69412321-69412368	K562	blood:	n/a	n/a
22	CEBPB	chr3:69389849-69390049	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:69402911-69403237	Hela-S3	cervix:	n/a	chr3:69403048-69403061
24	CHD1	chr3:69377163-69377629	GM12878	blood:	n/a	n/a
25	CHD2	chr3:69375694-69376467	GM12878	blood:	n/a	n/a
26	CREB1	chr3:69375773-69376527	GM12878	blood:	n/a	n/a
27	CREB1	chr3:69375891-69376403	GM12878	blood:	n/a	n/a
28	CTCF	chr3:69406472-69406539	GM13976	blood:	n/a	n/a
29	CTCF	chr3:69391914-69392007	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr3:69413440-69413590	AG04449	skin:	n/a	n/a
31	CTCF	chr3:69413380-69413530	NHEK	skin:	n/a	n/a
32	CTCF	chr3:69413320-69413470	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr3:69405487-69405608	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr3:69413482-69413546	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:69381813-69381843	GM19239	blood:	n/a	n/a
36	CTCF	chr3:69394361-69394426	Fibrobl	skin:	n/a	n/a
37	CTCF	chr3:69387066-69387133	GM13977	blood:	n/a	n/a
38	CTCF	chr3:69413500-69413650	BE2_C	brain:	n/a	n/a
39	CTCF	chr3:69413478-69413527	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:69385807-69385891	GM20000	blood:	n/a	n/a
41	CTCF	chr3:69413452-69413531	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:69413503-69413534	ProgFib	skin:	n/a	n/a
43	CTCF	chr3:69405511-69405554	Pancreas_OC	pancreas:	n/a	n/a
44	CUX1	chr3:69375950-69376391	GM12878	blood:	n/a	n/a
45	CUX1	chr3:69377383-69377514	GM12878	blood:	n/a	n/a
46	E2F4	chr3:69413490-69413794	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr3:69406504-69406666	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr3:69376016-69376801	GM12878	blood:	n/a	n/a
49	EBF1	chr3:69375984-69376420	GM12878	blood:	n/a	n/a
50	EBF1	chr3:69388943-69389094	GM12878	blood:	n/a	chr3:69389002-69389012

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69408925-69408975	SK-N-SH	brain:	n/a
2	chr3:69390063-69390113	LNCaP	prostate:	n/a
3	chr3:69402811-69402861	SKMC	muscle:	n/a
4	chr3:69390063-69390113	ovcar-3	ovarian:	n/a
5	chr3:69408925-69408975	HIPEpiC	eye:	n/a
6	chr3:69408925-69408975	H1-hESC	embryonic stem cell:	embryo
7	chr3:69390063-69390113	MCF-7	breast:	n/a
8	chr3:69408925-69408975	GM12892	blood:	n/a
9	chr3:69402811-69402861	GM12891	blood:	n/a
10	chr3:69402811-69402861	BE2_C	brain:	n/a
11	chr3:69390063-69390113	HRCEpiC	kidney:	n/a
12	chr3:69402811-69402861	HIPEpiC	eye:	n/a
13	chr3:69408925-69408975	Hepatocyte	liver:	n/a
14	chr3:69408925-69408975	HepG2	liver:	n/a
15	chr3:69390063-69390113	NHBE	bronchial:	n/a
16	chr3:69390063-69390113	PANC-1	pancreas:	n/a
17	chr3:69408925-69408975	IMR90	lung:	fetal
18	chr3:69408925-69408975	HRCEpiC	kidney:	n/a
19	chr3:69408925-69408975	BJ	skin:	n/a
20	chr3:69402811-69402861	NHDF-neo	bronchial:	n/a
21	chr3:69390063-69390113	HCPEpiC	choroid plexus:	n/a
22	chr3:69402811-69402861	HRE	kidney:	n/a
23	chr3:69390063-69390113	HCT-116	colon:	n/a
24	chr3:69390063-69390113	GM19239	blood:	n/a
25	chr3:69402811-69402861	H1-hESC	embryonic stem cell:	embryo
26	chr3:69402811-69402861	RPTEC	kidney:	n/a
27	chr3:69390063-69390113	NB4	blood:	n/a
28	chr3:69402811-69402861	HNPCEpiC	eye:	n/a
29	chr3:69390063-69390113	HMEC	breast:	n/a
30	chr3:69390063-69390113	Caco-2	colon:	n/a
31	chr3:69390063-69390113	HEK293	kidney:	embryo
32	chr3:69408925-69408975	AG04450	lung:	fetal
33	chr3:69390063-69390113	SK-N-SH	brain:	n/a
34	chr3:69402811-69402861	SK-N-SH_RA	brain:	n/a
35	chr3:69402811-69402861	BJ	skin:	n/a
36	chr3:69402811-69402861	K562	blood:	n/a
37	chr3:69402811-69402861	Hepatocyte	liver:	n/a
38	chr3:69408925-69408975	PANC-1	pancreas:	n/a
39	chr3:69408925-69408975	GM19239	blood:	n/a
40	chr3:69390063-69390113	AG10803	skin:	n/a
41	chr3:69402811-69402861	HEK293	kidney:	embryo
42	chr3:69408925-69408975	SK-N-SH_RA	brain:	n/a
43	chr3:69408925-69408975	SKMC	muscle:	n/a
44	chr3:69390063-69390113	ECC-1	luminal epithelium:	n/a
45	chr3:69390063-69390113	GM12878	blood:	n/a
46	chr3:69390063-69390113	SK-N-SH_RA	brain:	n/a
47	chr3:69390063-69390113	NT2-D1	testis:	n/a
48	chr3:69402811-69402861	CMK	blood:	n/a
49	chr3:69390063-69390113	AG09309	skin:	n/a
50	chr3:69402811-69402861	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:69373390..69375436-chr3:69478207..69481106,2	MCF-7	breast:
2	chr3:69374544..69375213-chr6:139764292..139765130,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMOD3-3	chr3:69383112-69383617	NONHSAT090359
2	lnc-LMOD3-3	chr3:69383323-69383617	NONHSAT090360
3	lnc-LMOD3-3	chr3:69385656-69385737	NONHSAT090360

No data

Variant related genes	Relation type
FRMD4B	TF binding region
FRMD4B	CpG island

Extended variants
information (count: 1720 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191500359	chr3:69374738-69374739	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564101024	chr3:69374787-69374788	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34428822	chr3:69374793-69374794	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536916176	chr3:69374912-69374913	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553715656	chr3:69374916-69374917	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566828253	chr3:69374920-69374921	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539085130	chr3:69374949-69374950	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78728909	chr3:69374993-69374994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187849907	chr3:69374994-69374995	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544374403	chr3:69375037-69375038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554441034	chr3:69375038-69375039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9876410	chr3:69375057-69375058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs191471149	chr3:69375079-69375080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560017878	chr3:69375092-69375093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531977559	chr3:69375094-69375095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146083122	chr3:69375124-69375125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144852048	chr3:69375133-69375134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72335731	chr3:69375134-69375135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397758184	chr3:69375144-69375145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562586602	chr3:69375158-69375159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531331812	chr3:69375200-69375201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548286477	chr3:69375233-69375234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371350022	chr3:69375270-69375271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567720693	chr3:69375333-69375334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183612461	chr3:69375354-69375355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559818210	chr3:69375373-69375374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547313080	chr3:69375433-69375434	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs567214674	chr3:69375439-69375440	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs539021168	chr3:69375460-69375461	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs552320195	chr3:69375472-69375473	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569257524	chr3:69375486-69375487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs186787290	chr3:69375503-69375504	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140084738	chr3:69375531-69375532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs555056176	chr3:69375560-69375561	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574245112	chr3:69375575-69375576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs529645412	chr3:69375647-69375648	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4855388	chr3:69375655-69375656	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs559404370	chr3:69375672-69375673	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553639066	chr3:69375677-69375678	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192654935	chr3:69375716-69375717	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144075613	chr3:69375724-69375725	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562314734	chr3:69375736-69375737	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576000724	chr3:69375740-69375741	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528504094	chr3:69375817-69375818	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs116641380	chr3:69375822-69375823	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs545380865	chr3:69375836-69375837	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs185494702	chr3:69375877-69375878	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs547250928	chr3:69375981-69375982	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs560747801	chr3:69376012-69376013	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs532667032	chr3:69376031-69376032	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:772 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69360600-69382200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:69366400-69376200	Enhancers	Brain Anterior Caudate	brain
3	chr3:69366800-69378200	Enhancers	Brain Hippocampus Middle	brain
4	chr3:69367200-69378400	Enhancers	Brain Substantia Nigra	brain
5	chr3:69367400-69374800	Enhancers	Brain Angular Gyrus	brain
6	chr3:69368400-69378200	Enhancers	Brain Cingulate Gyrus	brain
7	chr3:69369000-69377600	Weak transcription	Fetal Brain Female	brain
8	chr3:69369800-69376600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr3:69370200-69384000	Weak transcription	Left Ventricle	heart
10	chr3:69370400-69376600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:69370400-69379200	Weak transcription	Spleen	Spleen
12	chr3:69370600-69375800	Weak transcription	HUVEC	blood vessel
13	chr3:69371000-69375600	Weak transcription	Fetal Lung	lung
14	chr3:69371000-69377400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:69371400-69377000	Weak transcription	Fetal Stomach	stomach
16	chr3:69371600-69375600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:69371800-69380000	Weak transcription	Fetal Heart	heart
18	chr3:69372000-69375000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:69372200-69377400	Weak transcription	Ovary	ovary
20	chr3:69372200-69403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:69372400-69377200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr3:69372400-69380000	Weak transcription	NHEK	skin
23	chr3:69372800-69374800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr3:69373000-69375000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr3:69373000-69375800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:69373000-69376000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr3:69373200-69375800	Enhancers	Primary B cells from cord blood	blood
28	chr3:69373400-69375000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr3:69373400-69375400	Enhancers	GM12878-XiMat	blood
30	chr3:69373400-69376200	Enhancers	Fetal Thymus	thymus
31	chr3:69373600-69375400	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr3:69373600-69375400	Weak transcription	HSMMtube	muscle
33	chr3:69373600-69377400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr3:69373600-69378400	Enhancers	Primary B cells from peripheral blood	blood
35	chr3:69373800-69375000	Enhancers	Thymus	Thymus
36	chr3:69373800-69375600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr3:69373800-69375600	Weak transcription	HSMM	muscle
38	chr3:69373800-69380400	Weak transcription	Placenta	Placenta
39	chr3:69374000-69375800	Enhancers	Primary hematopoietic stem cells	blood
40	chr3:69374200-69375800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr3:69374200-69376200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr3:69374400-69375600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:69374400-69376000	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr3:69374400-69376600	Enhancers	Adipose Nuclei	Adipose
45	chr3:69374600-69375000	Enhancers	Primary T cells from cord blood	blood
46	chr3:69374600-69375000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr3:69374600-69375400	Enhancers	Dnd41	blood
48	chr3:69374600-69375600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr3:69374600-69375800	Weak transcription	Aorta	Aorta
50	chr3:69374600-69380400	Weak transcription	Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links