Variant report

Variant	esv1820988
Chromosome Location	chr2:98168868-98240470
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	chr2:98207224-98207615	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:98207279-98207593	K562	blood:	n/a	n/a
3	ATF1	chr2:98207276-98207536	K562	blood:	n/a	n/a
4	ATF1	chr2:98235903-98235915	K562	blood:	n/a	n/a
5	ATF3	chr2:98207210-98207581	K562	blood:	n/a	n/a
6	BATF	chr2:98207309-98207641	GM12878	blood:	n/a	n/a
7	BATF	chr2:98206887-98207071	GM12878	blood:	n/a	n/a
8	BATF	chr2:98207363-98207686	GM12878	blood:	n/a	n/a
9	BATF	chr2:98194694-98194913	GM12878	blood:	n/a	n/a
10	BATF	chr2:98206281-98206755	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:98207352-98207590	GM12878	blood:	n/a	chr2:98207572-98207579
12	BCL11A	chr2:98205341-98205570	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:98206444-98207010	GM12878	blood:	n/a	chr2:98206849-98206862 chr2:98206762-98206775
14	BCL11A	chr2:98219694-98219900	GM12878	blood:	n/a	n/a
15	BCLAF1	chr2:98207201-98207637	GM12878	blood:	n/a	chr2:98207572-98207579
16	BHLHE40	chr2:98207280-98207592	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:98206179-98206453	K562	blood:	n/a	n/a
18	BHLHE40	chr2:98206228-98206632	HepG2	liver:	n/a	n/a
19	BHLHE40	chr2:98206265-98206289	GM12878	blood:	n/a	n/a
20	BRCA1	chr2:98207285-98207646	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr2:98229993-98230316	K562	blood:	n/a	n/a
22	CBX3	chr2:98206082-98206466	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	CCNT2	chr2:98206271-98206359	K562	blood:	n/a	n/a
26	CEBPB	chr2:98212021-98212220	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:98212009-98212216	K562	blood:	n/a	n/a
28	CEBPB	chr2:98212022-98212221	HepG2	liver:	n/a	n/a
29	CEBPD	chr2:98206159-98206391	HepG2	liver:	n/a	n/a
30	CHD1	chr2:98207385-98207408	GM12878	blood:	n/a	n/a
31	CHD2	chr2:98206316-98206476	HepG2	liver:	n/a	n/a
32	CHD2	chr2:98206243-98206454	K562	blood:	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	chr2:98206306-98206498	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr2:98207380-98207530	SAEC	small airway:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
37	CTCF	chr2:98236121-98236207	GM12891	blood:	n/a	chr2:98236158-98236179
38	CTCF	chr2:98221682-98221835	MCF-7	breast:	n/a	chr2:98221775-98221793
39	CTCF	chr2:98206620-98206770	HFF	foreskin:	n/a	n/a
40	CTCF	chr2:98207298-98207573	Hela-S3	cervix:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
41	CTCF	chr2:98236069-98236243	MCF-7	breast:	n/a	chr2:98236229-98236237 chr2:98236158-98236179
42	CTCF	chr2:98221606-98221981	A549	lung:	n/a	chr2:98221775-98221793
43	CTCF	chr2:98206452-98206634	GM10248	blood:	n/a	n/a
44	CTCF	chr2:98236163-98236194	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr2:98236118-98236219	H1-hESC	embryonic stem cell:	n/a	chr2:98236158-98236179
46	CTCF	chr2:98207202-98207631	T-47D	breast:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
47	CTCF	chr2:98232957-98233026	MCF-7	breast:	n/a	chr2:98232970-98232988
48	CTCF	chr2:98207360-98207510	GM12869	blood:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
49	CTCF	chr2:98207380-98207530	AG04449	skin:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
50	CTCF	chr2:98207320-98207470	GM12801	blood:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98206095-98206145	HL-60	blood:	n/a
2	chr2:98207190-98207240	BJ	skin:	n/a
3	chr2:98206702-98206752	ProgFib	skin:	n/a
4	chr2:98206249-98206299	NH-A	brain:	n/a
5	chr2:98206175-98206225	H1-hESC	embryonic stem cell:	embryo
6	chr2:98206733-98206783	AoSMC	blood vessel:	n/a
7	chr2:98206702-98206752	Hela-S3	cervix:	n/a
8	chr2:98207190-98207240	T-47D	breast:	n/a
9	chr2:98207378-98207428	NHBE	bronchial:	n/a
10	chr2:98206175-98206225	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:98206733-98206783	HCF	heart:	n/a
12	chr2:98205903-98205953	H1-hESC	embryonic stem cell:	embryo
13	chr2:98206249-98206299	SAEC	small airway:	n/a
14	chr2:98206249-98206299	RPTEC	kidney:	n/a
15	chr2:98206702-98206752	Caco-2	colon:	n/a
16	chr2:98210494-98210544	NT2-D1	testis:	n/a
17	chr2:98210494-98210544	Jurkat	blood:	n/a
18	chr2:98206733-98206783	AG09319	gingival:	n/a
19	chr2:98206175-98206225	GM12878	blood:	n/a
20	chr2:98206095-98206145	HMEC	breast:	n/a
21	chr2:98205903-98205953	NB4	blood:	n/a
22	chr2:98206733-98206783	PFSK-1	brain:	n/a
23	chr2:98206175-98206225	AG09309	skin:	n/a
24	chr2:98206095-98206145	HAEpiC	amniotic membrane:	n/a
25	chr2:98207378-98207428	AG04450	lung:	fetal
26	chr2:98206175-98206225	HUVEC	blood vessel:	n/a
27	chr2:98210494-98210544	ovcar-3	ovarian:	n/a
28	chr2:98206175-98206225	SAEC	small airway:	n/a
29	chr2:98206175-98206225	A549	lung:	n/a
30	chr2:98206702-98206752	PANC-1	pancreas:	n/a
31	chr2:98205903-98205953	ECC-1	luminal epithelium:	n/a
32	chr2:98205903-98205953	GM12878	blood:	n/a
33	chr2:98206095-98206145	PrEC	prostate:	n/a
34	chr2:98207190-98207240	PFSK-1	brain:	n/a
35	chr2:98206175-98206225	AG04449	skin:	fetal
36	chr2:98206249-98206299	CMK	blood:	n/a
37	chr2:98205903-98205953	GM12891	blood:	n/a
38	chr2:98207190-98207240	HRCEpiC	kidney:	n/a
39	chr2:98207378-98207428	HL-60	blood:	n/a
40	chr2:98206702-98206752	AG04450	lung:	fetal
41	chr2:98206733-98206783	IMR90	lung:	fetal
42	chr2:98206733-98206783	HCT-116	colon:	n/a
43	chr2:98207378-98207428	SK-N-SH	brain:	n/a
44	chr2:98207378-98207428	RPTEC	kidney:	n/a
45	chr2:98207378-98207428	SAEC	small airway:	n/a
46	chr2:98206095-98206145	RPTEC	kidney:	n/a
47	chr2:98206095-98206145	GM12892	blood:	n/a
48	chr2:98210494-98210544	HEEpiC	esophagus:	n/a
49	chr2:98207378-98207428	BE2_C	brain:	n/a
50	chr2:98205903-98205953	GM12892	blood:	n/a

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

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

Extended variants
information (count: 2111 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386648416	chr2:98168868-98168869	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371097404	chr2:98168869-98168870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552478426	chr2:98168883-98168884	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569463225	chr2:98168884-98168885	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201336983	chr2:98168895-98168896	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189918397	chr2:98168908-98168909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10209395	chr2:98168912-98168913	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs531831339	chr2:98168939-98168940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180811586	chr2:98168941-98168942	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555211427	chr2:98168951-98168952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565391336	chr2:98168963-98168964	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533888576	chr2:98169019-98169020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553798105	chr2:98169041-98169042	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186205326	chr2:98169047-98169048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546314231	chr2:98169076-98169077	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190379113	chr2:98169082-98169083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532468575	chr2:98169098-98169099	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10169456	chr2:98169110-98169111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs145277465	chr2:98169114-98169115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs118031909	chr2:98169137-98169138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540222066	chr2:98169168-98169169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560224076	chr2:98169173-98169174	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530099600	chr2:98169226-98169227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532085957	chr2:98169257-98169258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182013155	chr2:98169263-98169264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59824983	chr2:98169326-98169327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9677078	chr2:98169354-98169355	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs529546521	chr2:98169392-98169393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75989672	chr2:98169431-98169432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531893725	chr2:98169438-98169439	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548378345	chr2:98169439-98169440	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547651205	chr2:98169447-98169448	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575427933	chr2:98169457-98169458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566016797	chr2:98169461-98169462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9677528	chr2:98169479-98169480	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs9679287	chr2:98169519-98169520	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs9677087	chr2:98169544-98169545	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs539474252	chr2:98169548-98169549	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9679293	chr2:98169583-98169584	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs576460054	chr2:98169616-98169617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544390180	chr2:98169649-98169650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554843519	chr2:98169658-98169659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574768137	chr2:98169669-98169670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555068279	chr2:98169674-98169675	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540560227	chr2:98169689-98169690	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373424809	chr2:98169727-98169728	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12998184	chr2:98169742-98169743	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
48	rs368811626	chr2:98169755-98169756	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199655122	chr2:98169799-98169800	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200751592	chr2:98169816-98169817	Weak transcription Strong transcription Enhancers	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:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98140800-98187600	Weak transcription	Fetal Stomach	stomach
2	chr2:98142800-98171400	Weak transcription	Fetal Intestine Small	intestine
3	chr2:98142800-98174800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:98142800-98177800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:98143600-98205600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:98153400-98189800	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:98153600-98178600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:98154200-98185200	Weak transcription	Fetal Kidney	kidney
9	chr2:98154200-98187000	Weak transcription	Left Ventricle	heart
10	chr2:98154800-98169600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:98154800-98174800	Weak transcription	Placenta	Placenta
12	chr2:98155200-98176600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:98156200-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:98156800-98204200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr2:98160200-98205800	Weak transcription	K562	blood
16	chr2:98160800-98175800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:98161200-98171000	Weak transcription	HMEC	breast
18	chr2:98161400-98171000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr2:98161400-98172600	Weak transcription	Aorta	Aorta
20	chr2:98161400-98174400	Weak transcription	Pancreas	Pancrea
21	chr2:98161400-98174800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:98161400-98176600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr2:98161400-98176600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr2:98161400-98176800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:98161400-98177400	Weak transcription	Brain Substantia Nigra	brain
26	chr2:98161400-98178400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr2:98161400-98185800	Weak transcription	NHEK	skin
28	chr2:98161600-98170000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr2:98161800-98170800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr2:98162200-98176400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr2:98162400-98172600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:98162600-98173400	Strong transcription	Primary T cells from cord blood	blood
33	chr2:98162600-98177000	Weak transcription	Lung	lung
34	chr2:98163800-98172800	Weak transcription	Psoas Muscle	Psoas
35	chr2:98164000-98204600	Weak transcription	A549	lung
36	chr2:98164200-98172600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr2:98164200-98181000	Weak transcription	Hela-S3	cervix
38	chr2:98164400-98174600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:98164400-98175600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr2:98164400-98175600	Weak transcription	NHLF	lung
41	chr2:98164400-98179800	Weak transcription	Spleen	Spleen
42	chr2:98164800-98172800	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr2:98164800-98176000	Weak transcription	HSMMtube	muscle
44	chr2:98164800-98178800	Weak transcription	Right Ventricle	heart
45	chr2:98165000-98172200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr2:98165000-98172600	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr2:98165400-98173400	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr2:98165400-98174800	Weak transcription	Gastric	stomach
49	chr2:98165600-98171200	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr2:98165600-98171200	Weak transcription	NH-A	brain

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