Variant report

Variant	esv1842036
Chromosome Location	chr2:98155850-98257451
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	ARID3A	chr2:98207279-98207593	K562	blood:	n/a	n/a
2	ARID3A	chr2:98207224-98207615	HepG2	liver:	n/a	n/a
3	ATF1	chr2:98235903-98235915	K562	blood:	n/a	n/a
4	ATF1	chr2:98207276-98207536	K562	blood:	n/a	n/a
5	ATF3	chr2:98207210-98207581	K562	blood:	n/a	n/a
6	BATF	chr2:98206887-98207071	GM12878	blood:	n/a	n/a
7	BATF	chr2:98194694-98194913	GM12878	blood:	n/a	n/a
8	BATF	chr2:98206281-98206755	GM12878	blood:	n/a	n/a
9	BATF	chr2:98207309-98207641	GM12878	blood:	n/a	n/a
10	BATF	chr2:98207363-98207686	GM12878	blood:	n/a	n/a
11	BATF	chr2:98158810-98158993	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:98206444-98207010	GM12878	blood:	n/a	chr2:98206849-98206862 chr2:98206762-98206775
13	BCL11A	chr2:98207352-98207590	GM12878	blood:	n/a	chr2:98207572-98207579
14	BCL11A	chr2:98205341-98205570	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:98219694-98219900	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:98207201-98207637	GM12878	blood:	n/a	chr2:98207572-98207579
17	BHLHE40	chr2:98206228-98206632	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:98207280-98207592	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:98206265-98206289	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:98206179-98206453	K562	blood:	n/a	n/a
21	BRCA1	chr2:98207285-98207646	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr2:98229993-98230316	K562	blood:	n/a	n/a
23	CBX3	chr2:98206107-98207533	K562	blood:	n/a	n/a
24	CBX3	chr2:98207164-98207600	K562	blood:	n/a	n/a
25	CBX3	chr2:98206082-98206466	K562	blood:	n/a	n/a
26	CCNT2	chr2:98206271-98206359	K562	blood:	n/a	n/a
27	CEBPB	chr2:98212022-98212221	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:98212021-98212220	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:98212009-98212216	K562	blood:	n/a	n/a
30	CEBPD	chr2:98206159-98206391	HepG2	liver:	n/a	n/a
31	CHD1	chr2:98207385-98207408	GM12878	blood:	n/a	n/a
32	CHD2	chr2:98206306-98206498	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr2:98207321-98207531	GM12878	blood:	n/a	n/a
34	CHD2	chr2:98207250-98207471	HepG2	liver:	n/a	n/a
35	CHD2	chr2:98206243-98206454	K562	blood:	n/a	n/a
36	CHD2	chr2:98206316-98206476	HepG2	liver:	n/a	n/a
37	CTCF	chr2:98206620-98206770	HFF	foreskin:	n/a	n/a
38	CTCF	chr2:98207300-98207450	HVMF	connective:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
39	CTCF	chr2:98207084-98207557	MCF-7	breast:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
40	CTCF	chr2:98221700-98221831	K562	blood:	n/a	chr2:98221775-98221793
41	CTCF	chr2:98207380-98207530	HCPEpiC	choroid plexus:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
42	CTCF	chr2:98206728-98206934	Medullo	brain:	n/a	chr2:98206828-98206841
43	CTCF	chr2:98236065-98236251	MCF-7	breast:	n/a	chr2:98236229-98236237 chr2:98236158-98236179
44	CTCF	chr2:98206726-98206917	Hela-S3	cervix:	n/a	chr2:98206828-98206841
45	CTCF	chr2:98207320-98207470	NHLF	lung:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
46	CTCF	chr2:98207286-98207638	Medullo	brain:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
47	CTCF	chr2:98206663-98207012	GM10248	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
48	CTCF	chr2:98207400-98207550	A549	lung:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
49	CTCF	chr2:98207126-98207729	K562	blood:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
50	CTCF	chr2:98174073-98174120	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98206702-98206752	HepG2	liver:	n/a
2	chr2:98206702-98206752	HepG2	liver:	n/a
3	chr2:98207378-98207428	NHBE	bronchial:	n/a
4	chr2:98207190-98207240	HCT-116	colon:	n/a
5	chr2:98207378-98207428	H1-hESC	embryonic stem cell:	embryo
6	chr2:98206733-98206783	HRPEpiC	eye:	n/a
7	chr2:98206249-98206299	U87	brain:	n/a
8	chr2:98205903-98205953	HCPEpiC	choroid plexus:	n/a
9	chr2:98206733-98206783	HIPEpiC	eye:	n/a
10	chr2:98206702-98206752	A549	lung:	n/a
11	chr2:98205903-98205953	SK-N-SH_RA	brain:	n/a
12	chr2:98206733-98206783	A549	lung:	n/a
13	chr2:98206095-98206145	HCF	heart:	n/a
14	chr2:98206702-98206752	NHBE	bronchial:	n/a
15	chr2:98206249-98206299	Jurkat	blood:	n/a
16	chr2:98206249-98206299	HCPEpiC	choroid plexus:	n/a
17	chr2:98210494-98210544	PFSK-1	brain:	n/a
18	chr2:98205903-98205953	HUVEC	blood vessel:	n/a
19	chr2:98207378-98207428	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:98207190-98207240	NHBE	bronchial:	n/a
21	chr2:98210494-98210544	U87	brain:	n/a
22	chr2:98256494-98256544	GM12891	blood:	n/a
23	chr2:98210494-98210544	HIPEpiC	eye:	n/a
24	chr2:98205903-98205953	GM12891	blood:	n/a
25	chr2:98256494-98256544	NT2-D1	testis:	n/a
26	chr2:98207190-98207240	Hepatocyte	liver:	n/a
27	chr2:98256494-98256544	MCF-7	breast:	n/a
28	chr2:98206095-98206145	GM06990	blood:	n/a
29	chr2:98205903-98205953	HAEpiC	amniotic membrane:	n/a
30	chr2:98206249-98206299	GM12878	blood:	n/a
31	chr2:98207378-98207428	HepG2	liver:	n/a
32	chr2:98207378-98207428	HCF	heart:	n/a
33	chr2:98207378-98207428	SAEC	small airway:	n/a
34	chr2:98207190-98207240	BE2_C	brain:	n/a
35	chr2:98206702-98206752	GM06990	blood:	n/a
36	chr2:98206733-98206783	HRE	kidney:	n/a
37	chr2:98206702-98206752	Jurkat	blood:	n/a
38	chr2:98206249-98206299	MCF-7	breast:	n/a
39	chr2:98206733-98206783	ovcar-3	ovarian:	n/a
40	chr2:98210494-98210544	Jurkat	blood:	n/a
41	chr2:98207190-98207240	Hela-S3	cervix:	n/a
42	chr2:98206702-98206752	SAEC	small airway:	n/a
43	chr2:98207190-98207240	AG04450	lung:	fetal
44	chr2:98206175-98206225	AG09309	skin:	n/a
45	chr2:98207378-98207428	NT2-D1	testis:	n/a
46	chr2:98206095-98206145	GM12891	blood:	n/a
47	chr2:98206733-98206783	HCPEpiC	choroid plexus:	n/a
48	chr2:98206249-98206299	AG04450	lung:	fetal
49	chr2:98206702-98206752	LNCaP	prostate:	n/a
50	chr2:98207378-98207428	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:98206110..98207769-chr2:98279652..98281540,2	K562	blood:
2	chr2:98243278..98243852-chr2:98313428..98314134,2	MCF-7	breast:
3	chr2:98207345..98207911-chr2:98364591..98365105,3	K562	blood:
4	chr2:98207000..98207853-chr2:219712161..219712679,2	MCF-7	breast:
5	chr2:98207030..98207867-chr2:98316437..98317264,2	MCF-7	breast:
6	chr2:98207335..98207918-chr2:98313479..98314662,4	MCF-7	breast:
7	chr2:98205848..98207835-chr2:98279004..98283186,3	MCF-7	breast:
8	chr2:98236811..98238337-chr2:98279045..98280683,2	K562	blood:
9	chr2:98255861..98257628-chr2:98260670..98262537,2	K562	blood:
10	chr2:98204043..98208769-chr2:98260858..98263741,4	MCF-7	breast:
11	chr2:98205832..98206585-chr20:2450969..2451709,2	NB4	blood:
12	chr2:98207030..98207891-chr2:98316572..98317381,2	K562	blood:
13	chr2:98206697..98208046-chr2:98313463..98314373,16	MCF-7	breast:
14	chr2:96658361..96659117-chr2:98208510..98209019,2	MCF-7	breast:
15	chr2:98242376..98244442-chr2:98262339..98264310,2	K562	blood:
16	chr2:98206925..98207973-chr2:98313358..98314529,26	K562	blood:
17	chr11:65274173..65274684-chr2:98182548..98183048,2	Hela-S3	cervix:
18	chr2:98201716..98203846-chr2:98280440..98282039,2	K562	blood:
19	chr2:98207043..98207962-chr2:98341661..98342410,2	MCF-7	breast:
20	chr2:98206838..98208035-chr2:98280277..98281403,5	MCF-7	breast:
21	chr2:98250388..98251913-chr2:98260315..98262590,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTR1B-5	chr2:98166049-98166705	NONHSAT072653
2	lnc-ACTR1B-5	chr2:98164470-98165954	NONHSAT072653

Variant related genes	Relation type
ANKRD36B	TF binding region
UBTFL6	TF binding region
ANKRD36B	CpG island
UBTFL6	CpG island
ENSG00000228486	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000135940	chromatin interactions
ENSG00000201806	chromatin interactions

Extended variants
information (count: 2950 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2950 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551552597	chr2:98155870-98155871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs6737245	chr2:98155915-98155916	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs536934646	chr2:98155944-98155945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3970447	chr2:98155946-98155947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3970446	chr2:98155963-98155964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4069272	chr2:98155966-98155967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562633102	chr2:98156023-98156024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2309075	chr2:98156059-98156060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567437340	chr2:98156064-98156065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2309074	chr2:98156085-98156086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6740279	chr2:98156087-98156088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2309073	chr2:98156110-98156111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529752993	chr2:98156124-98156125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536210629	chr2:98156137-98156138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552704599	chr2:98156139-98156140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2871109	chr2:98156147-98156148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572890377	chr2:98156164-98156165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544816578	chr2:98156174-98156175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189390776	chr2:98156240-98156241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373406704	chr2:98156349-98156350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548206329	chr2:98156353-98156354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546668314	chr2:98156357-98156358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575936878	chr2:98156393-98156394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199679277	chr2:98156414-98156415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181777503	chr2:98156421-98156422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188739692	chr2:98156433-98156434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561530001	chr2:98156468-98156469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186892734	chr2:98156514-98156515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546924269	chr2:98156540-98156541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560334033	chr2:98156575-98156576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2442235	chr2:98156600-98156601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191410935	chr2:98156622-98156623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552426780	chr2:98156659-98156660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571090346	chr2:98156665-98156666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536823787	chr2:98156677-98156678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376050070	chr2:98156731-98156732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567183267	chr2:98156828-98156829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2442236	chr2:98156946-98156947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2442237	chr2:98156954-98156955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536199012	chr2:98156959-98156960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552924312	chr2:98156970-98156971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572783728	chr2:98156993-98156994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538704286	chr2:98156995-98156996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558654954	chr2:98157020-98157021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575425195	chr2:98157101-98157102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544772601	chr2:98157106-98157107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555201950	chr2:98157141-98157142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575076438	chr2:98157174-98157175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540614244	chr2:98157191-98157192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2442238	chr2:98157200-98157201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98140800-98187600	Weak transcription	Fetal Stomach	stomach
2	chr2:98141800-98161000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:98141800-98162800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:98142000-98168000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr2:98142800-98156000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:98142800-98162200	Weak transcription	Primary B cells from cord blood	blood
7	chr2:98142800-98165000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr2:98142800-98171400	Weak transcription	Fetal Intestine Small	intestine
9	chr2:98142800-98174800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:98142800-98177800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr2:98143600-98167600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:98143600-98205600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:98144200-98156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:98144600-98165200	Weak transcription	Brain Germinal Matrix	brain
15	chr2:98147800-98168000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr2:98149600-98167600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr2:98151600-98162200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr2:98151600-98165000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:98151800-98165400	Weak transcription	Fetal Muscle Leg	muscle
20	chr2:98152000-98162600	Weak transcription	Fetal Lung	lung
21	chr2:98152000-98163200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr2:98152400-98162600	Weak transcription	Adipose Nuclei	Adipose
23	chr2:98152400-98162600	Weak transcription	Fetal Thymus	thymus
24	chr2:98152600-98163600	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr2:98152800-98158400	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr2:98152800-98163800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:98153000-98166800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr2:98153200-98157000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:98153400-98189800	Weak transcription	Colon Smooth Muscle	Colon
30	chr2:98153600-98178600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr2:98153800-98156400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:98153800-98167200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr2:98154000-98156400	Strong transcription	Ovary	ovary
34	chr2:98154200-98162000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr2:98154200-98165400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:98154200-98168000	Weak transcription	Fetal Intestine Large	intestine
37	chr2:98154200-98185200	Weak transcription	Fetal Kidney	kidney
38	chr2:98154200-98187000	Weak transcription	Left Ventricle	heart
39	chr2:98154400-98166800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr2:98154600-98162600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr2:98154800-98162600	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:98154800-98169600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:98154800-98174800	Weak transcription	Placenta	Placenta
44	chr2:98155200-98176600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:98155400-98156200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:98155400-98162600	Weak transcription	Primary T cells from cord blood	blood
47	chr2:98155400-98165200	Weak transcription	Liver	Liver
48	chr2:98155800-98156200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr2:98155800-98156400	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr2:98155800-98156400	Strong transcription	Fetal Brain Female	brain

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