Variant report

Variant	esv34280
Chromosome Location	chr3:142887460-142962075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:427)
Chromatin interactive
region (count:77)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142900853-142901159	K562	blood:	n/a	n/a
2	ARID3A	chr3:142897049-142897053	K562	blood:	n/a	n/a
3	ARID3A	chr3:142887160-142887701	K562	blood:	n/a	n/a
4	ARID3A	chr3:142902142-142902812	K562	blood:	n/a	n/a
5	ATF1	chr3:142896868-142897147	K562	blood:	n/a	n/a
6	ATF1	chr3:142887275-142887709	K562	blood:	n/a	n/a
7	ATF2	chr3:142899282-142899641	GM12878	blood:	n/a	n/a
8	ATF2	chr3:142925940-142926781	GM12878	blood:	n/a	n/a
9	ATF2	chr3:142926094-142926643	GM12878	blood:	n/a	n/a
10	ATF3	chr3:142887373-142887703	K562	blood:	n/a	n/a
11	ATF3	chr3:142941383-142941722	K562	blood:	n/a	n/a
12	BACH1	chr3:142926292-142926562	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:142926223-142926583	K562	blood:	n/a	n/a
14	BATF	chr3:142896967-142897183	GM12878	blood:	n/a	chr3:142897061-142897072
15	BATF	chr3:142896728-142896940	GM12878	blood:	n/a	n/a
16	BATF	chr3:142926120-142926589	GM12878	blood:	n/a	n/a
17	BATF	chr3:142896975-142897185	GM12878	blood:	n/a	chr3:142897061-142897072
18	BCL11A	chr3:142926100-142926557	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:142896930-142897147	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:142926060-142926545	GM12878	blood:	n/a	n/a
21	BCL3	chr3:142925964-142926581	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:142889996-142890544	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:142926050-142926724	GM12878	blood:	n/a	n/a
24	BCLAF1	chr3:142925723-142926725	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:142926070-142926539	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:142887394-142887703	K562	blood:	n/a	n/a
27	BHLHE40	chr3:142941367-142941680	K562	blood:	n/a	n/a
28	BHLHE40	chr3:142889636-142889695	GM12878	blood:	n/a	n/a
29	CBX3	chr3:142941254-142941740	K562	blood:	n/a	n/a
30	CBX3	chr3:142914454-142914881	K562	blood:	n/a	n/a
31	CBX3	chr3:142887276-142888091	K562	blood:	n/a	n/a
32	CBX3	chr3:142911803-142912166	K562	blood:	n/a	n/a
33	CBX3	chr3:142892097-142892462	K562	blood:	n/a	n/a
34	CBX3	chr3:142889073-142890041	K562	blood:	n/a	n/a
35	CBX3	chr3:142892077-142892498	K562	blood:	n/a	n/a
36	CBX3	chr3:142896742-142897236	K562	blood:	n/a	n/a
37	CBX3	chr3:142902085-142903026	K562	blood:	n/a	n/a
38	CCNT2	chr3:142900846-142901134	K562	blood:	n/a	n/a
39	CCNT2	chr3:142887290-142887770	K562	blood:	n/a	chr3:142887495-142887515
40	CCNT2	chr3:142902198-142902830	K562	blood:	n/a	chr3:142902508-142902528
41	CCNT2	chr3:142941447-142941639	K562	blood:	n/a	n/a
42	CCNT2	chr3:142936308-142936485	K562	blood:	n/a	n/a
43	CEBPB	chr3:142935848-142936007	K562	blood:	n/a	n/a
44	CEBPB	chr3:142902017-142902206	H1-hESC	embryonic stem cell:	n/a	chr3:142902094-142902105
45	CEBPB	chr3:142901738-142902685	K562	blood:	n/a	chr3:142902094-142902105
46	CEBPB	chr3:142898261-142898325	K562	blood:	n/a	n/a
47	CEBPB	chr3:142901955-142902272	HepG2	liver:	n/a	chr3:142902094-142902105
48	CEBPB	chr3:142923465-142923583	K562	blood:	n/a	n/a
49	CEBPB	chr3:142935866-142935999	A549	lung:	n/a	n/a
50	CEBPB	chr3:142901818-142902340	K562	blood:	n/a	chr3:142902094-142902105

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:142895375-142895425	HCPEpiC	choroid plexus:	n/a
2	chr3:142890118-142890168	HL-60	blood:	n/a
3	chr3:142895279-142895329	GM12878	blood:	n/a
4	chr3:142895861-142895911	NT2-D1	testis:	n/a
5	chr3:142890118-142890168	IMR90	lung:	fetal
6	chr3:142895861-142895911	LNCaP	prostate:	n/a
7	chr3:142888303-142888353	RPTEC	kidney:	n/a
8	chr3:142895861-142895911	Caco-2	colon:	n/a
9	chr3:142893947-142893997	HRPEpiC	eye:	n/a
10	chr3:142895375-142895425	CMK	blood:	n/a
11	chr3:142895861-142895911	ProgFib	skin:	n/a
12	chr3:142890118-142890168	H1-hESC	embryonic stem cell:	embryo
13	chr3:142895861-142895911	NH-A	brain:	n/a
14	chr3:142893947-142893997	GM12878	blood:	n/a
15	chr3:142926178-142926228	HCM	heart:	n/a
16	chr3:142926178-142926228	H1-hESC	embryonic stem cell:	embryo
17	chr3:142895279-142895329	NH-A	brain:	n/a
18	chr3:142895279-142895329	MCF-7	breast:	n/a
19	chr3:142926178-142926228	RPTEC	kidney:	n/a
20	chr3:142926178-142926228	IMR90	lung:	fetal
21	chr3:142893947-142893997	IMR90	lung:	fetal
22	chr3:142893947-142893997	NHDF-neo	bronchial:	n/a
23	chr3:142890118-142890168	HRCEpiC	kidney:	n/a
24	chr3:142895375-142895425	HRCEpiC	kidney:	n/a
25	chr3:142895279-142895329	HL-60	blood:	n/a
26	chr3:142895861-142895911	MCF-7	breast:	n/a
27	chr3:142926178-142926228	NH-A	brain:	n/a
28	chr3:142926178-142926228	K562	blood:	n/a
29	chr3:142888303-142888353	BE2_C	brain:	n/a
30	chr3:142890118-142890168	GM19239	blood:	n/a
31	chr3:142893947-142893997	HCT-116	colon:	n/a
32	chr3:142895861-142895911	K562	blood:	n/a
33	chr3:142890118-142890168	HAEpiC	amniotic membrane:	n/a
34	chr3:142895861-142895911	HCM	heart:	n/a
35	chr3:142895279-142895329	HIPEpiC	eye:	n/a
36	chr3:142890118-142890168	GM12891	blood:	n/a
37	chr3:142895375-142895425	NHBE	bronchial:	n/a
38	chr3:142895279-142895329	GM12892	blood:	n/a
39	chr3:142895279-142895329	AG09309	skin:	n/a
40	chr3:142895279-142895329	U87	brain:	n/a
41	chr3:142895375-142895425	Hela-S3	cervix:	n/a
42	chr3:142888303-142888353	MCF-7	breast:	n/a
43	chr3:142888303-142888353	T-47D	breast:	n/a
44	chr3:142895375-142895425	NB4	blood:	n/a
45	chr3:142895375-142895425	RPTEC	kidney:	n/a
46	chr3:142890118-142890168	T-47D	breast:	n/a
47	chr3:142895861-142895911	GM19239	blood:	n/a
48	chr3:142895279-142895329	SAEC	small airway:	n/a
49	chr3:142895861-142895911	NB4	blood:	n/a
50	chr3:142895279-142895329	H1-hESC	embryonic stem cell:	embryo

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:142842312..142844525-chr3:142920222..142922927,2	K562	blood:
2	chr3:142918300..142920442-chr3:142921412..142923086,3	K562	blood:
3	chr3:142954351..142956458-chr3:142960764..142964653,3	K562	blood:
4	chr3:142900165..142901896-chr3:142950119..142953076,2	K562	blood:
5	chr3:142935120..142937637-chr3:142937877..142939570,2	MCF-7	breast:
6	chr3:142917101..142918800-chr3:142923414..142925582,2	K562	blood:
7	chr3:142904057..142907019-chr3:142910125..142912001,3	K562	blood:
8	chr3:142895472..142897996-chr3:143019191..143020977,2	K562	blood:
9	chr3:142935120..142937637-chr3:142937877..142939570,2	MCF-7	breast:
10	chr3:142899439..142901462-chr3:142905793..142908005,2	K562	blood:
11	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:
12	chr3:142910443..142912503-chr3:142926393..142928620,2	K562	blood:
13	chr3:142908825..142914026-chr3:142914356..142919906,7	K562	blood:
14	chr3:142925537..142928123-chr3:142932131..142934327,2	K562	blood:
15	chr3:142889235..142895118-chr3:142897231..142901814,7	K562	blood:
16	chr3:142943499..142945080-chr3:143037580..143040276,2	K562	blood:
17	chr3:142955679..142958275-chr3:142964132..142966713,2	K562	blood:
18	chr3:142926220..142927861-chr3:142959735..142962076,2	K562	blood:
19	chr3:142945884..142947891-chr3:142949125..142952561,4	K562	blood:
20	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:
21	chr3:142940072..142941625-chr3:142954271..142955900,2	K562	blood:
22	chr3:142930578..142932212-chr3:142932647..142934719,2	K562	blood:
23	chr3:142908825..142914026-chr3:142914356..142919906,7	K562	blood:
24	chr3:142951557..142953116-chr3:142953358..142955384,2	K562	blood:
25	chr3:142938667..142941480-chr3:142941937..142946054,4	K562	blood:
26	chr3:142930578..142932212-chr3:142932647..142934719,2	K562	blood:
27	chr3:142948047..142951312-chr3:142952653..142957193,4	K562	blood:
28	chr3:142929008..142930843-chr3:142953006..142954925,2	K562	blood:
29	chr3:142929546..142932145-chr3:142933219..142936261,3	K562	blood:
30	chr3:142922192..142925185-chr3:142931380..142934358,2	K562	blood:
31	chr3:142837194..142839590-chr3:142902275..142903779,2	K562	blood:
32	chr3:142956744..142958765-chr3:142965944..142967632,2	K562	blood:
33	chr3:142875650..142878540-chr3:142902217..142903747,2	K562	blood:
34	chr3:142921678..142924452-chr3:142925121..142926893,2	K562	blood:
35	chr3:142914308..142916627-chr3:142918947..142921480,2	K562	blood:
36	chr3:142899439..142901462-chr3:142905793..142908005,2	K562	blood:
37	chr3:142926220..142927861-chr3:142959735..142962076,2	K562	blood:
38	chr3:142887670..142889227-chr3:142893884..142896662,2	K562	blood:
39	chr3:142907861..142909717-chr3:142911559..142913814,2	K562	blood:
40	chr3:142947986..142949747-chr3:143028626..143030178,2	K562	blood:
41	chr3:142951557..142953116-chr3:142953358..142955384,2	K562	blood:
42	chr3:142929008..142930843-chr3:142953006..142954925,2	K562	blood:
43	chr3:142889235..142895118-chr3:142897231..142901814,7	K562	blood:
44	chr3:142907861..142909717-chr3:142911559..142913814,2	K562	blood:
45	chr3:142938475..142939430-chr3:142950578..142951319,2	MCF-7	breast:
46	chr3:142922192..142925185-chr3:142931380..142934358,2	K562	blood:
47	chr3:142948047..142951312-chr3:142952653..142957193,4	K562	blood:
48	chr3:142900165..142901896-chr3:142950119..142953076,2	K562	blood:
49	chr3:142925537..142928123-chr3:142932131..142934327,2	K562	blood:
50	chr3:142917669..142921522-chr3:142924910..142927664,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-10	chr3:142951419-142951544	l_2486_chr3:142951418-142976230_ovary
2	lnc-CHST2-10	chr3:142951611-142951872	l_2486_chr3:142951418-142976230_ovary

No data

Variant related genes	Relation type
PBX2P1	TF binding region
PBX2P1	CpG island
ENSG00000175040	chromatin interactions
ENSG00000244171	chromatin interactions
ENSG00000211483	chromatin interactions

Extended variants
information (count: 2880 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1449867	chr3:142887460-142887461	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559516392	chr3:142887472-142887473	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577736733	chr3:142887482-142887483	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556274496	chr3:142887522-142887523	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73866410	chr3:142887526-142887527	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73159650	chr3:142887564-142887565	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541531068	chr3:142887603-142887604	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549043892	chr3:142887695-142887696	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs560818979	chr3:142887736-142887737	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35804267	chr3:142887776-142887777	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528804204	chr3:142887780-142887781	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs546942932	chr3:142887782-142887783	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571888680	chr3:142887825-142887826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs35069191	chr3:142887827-142887828	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538898828	chr3:142887838-142887839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146857763	chr3:142887849-142887850	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140704485	chr3:142887861-142887862	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs7649342	chr3:142887871-142887872	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs554556022	chr3:142887887-142887888	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145920599	chr3:142887923-142887924	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534941406	chr3:142887954-142887955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs553017605	chr3:142887990-142887991	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs146662579	chr3:142888027-142888028	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs59013311	chr3:142888039-142888040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs17572584	chr3:142888043-142888044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs61157099	chr3:142888059-142888060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs140045665	chr3:142888066-142888067	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs150302946	chr3:142888097-142888098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542704252	chr3:142888102-142888103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560881352	chr3:142888109-142888110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147475344	chr3:142888129-142888130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs188744851	chr3:142888156-142888157	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569911960	chr3:142888186-142888187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371534304	chr3:142888296-142888297	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs137965140	chr3:142888303-142888304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149493152	chr3:142888304-142888305	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs193215006	chr3:142888311-142888312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs569071480	chr3:142888344-142888345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs183625926	chr3:142888378-142888379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548251169	chr3:142888396-142888397	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs10513192	chr3:142888404-142888405	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs377090498	chr3:142888415-142888416	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564670735	chr3:142888419-142888420	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs558900518	chr3:142888450-142888451	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370623194	chr3:142888479-142888480	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531905591	chr3:142888564-142888565	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557202030	chr3:142888586-142888587	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs5853095	chr3:142888590-142888591	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs397806365	chr3:142888591-142888592	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1530266	chr3:142888606-142888607	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142881200-142888600	Enhancers	Primary T cells from cord blood	blood
2	chr3:142882000-142888400	Enhancers	Dnd41	blood
3	chr3:142882000-142891600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr3:142882200-142889000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr3:142882400-142889600	Enhancers	Fetal Thymus	thymus
6	chr3:142882800-142889200	Weak transcription	Fetal Stomach	stomach
7	chr3:142883600-142887800	Weak transcription	Primary B cells from cord blood	blood
8	chr3:142884000-142891600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr3:142884200-142887800	Enhancers	NHEK	skin
10	chr3:142884200-142891200	Enhancers	K562	blood
11	chr3:142884400-142888200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr3:142884600-142887600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr3:142884600-142889000	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr3:142884600-142889400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:142884800-142888000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr3:142884800-142889400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr3:142885200-142887600	Weak transcription	Thymus	Thymus
18	chr3:142885200-142889000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr3:142885400-142888000	Weak transcription	Fetal Lung	lung
20	chr3:142885600-142890200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:142885800-142888200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:142886000-142887800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:142886000-142888000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:142886000-142888000	Enhancers	HMEC	breast
25	chr3:142886200-142887600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:142886200-142887800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:142886200-142888600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr3:142886200-142889200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr3:142886200-142889400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr3:142886200-142889800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr3:142886400-142887800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr3:142886400-142887800	Enhancers	Hela-S3	cervix
33	chr3:142886400-142887800	Enhancers	Osteobl	bone
34	chr3:142886400-142888600	Weak transcription	GM12878-XiMat	blood
35	chr3:142886400-142889200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr3:142886400-142889800	Enhancers	Primary hematopoietic stem cells	blood
37	chr3:142886600-142887600	Enhancers	HSMM	muscle
38	chr3:142886600-142887600	Enhancers	NHDF-Ad	bronchial
39	chr3:142886600-142887800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr3:142886600-142887800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr3:142886600-142887800	Enhancers	NH-A	brain
42	chr3:142886600-142887800	Enhancers	NHLF	lung
43	chr3:142886600-142888000	Enhancers	HUVEC	blood vessel
44	chr3:142886600-142889200	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr3:142886600-142889200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:142886600-142890400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr3:142886800-142887800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr3:142886800-142890400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr3:142886800-142891400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:142887000-142887600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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