Variant report

Variant	nsv885861
Chromosome Location	chr6:44837356-45043618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:961)
CpG islands
(count:183)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45017618-45017640	K562	blood:	n/a	n/a
2	ARID3A	chr6:44888556-44889970	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:45011822-45012263	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:44900932-44900942	K562	blood:	n/a	n/a
5	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
6	ARID3A	chr6:45025490-45025613	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:44918920-44919276	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:44907927-44908749	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:44942228-44942585	K562	blood:	n/a	n/a
10	ARID3A	chr6:45017086-45017200	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
12	ATF1	chr6:44876296-44876496	K562	blood:	n/a	n/a
13	ATF1	chr6:44888645-44888963	K562	blood:	n/a	n/a
14	ATF1	chr6:45016978-45017291	K562	blood:	n/a	n/a
15	ATF1	chr6:45025523-45025589	K562	blood:	n/a	n/a
16	ATF1	chr6:44893099-44893531	K562	blood:	n/a	n/a
17	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
18	ATF2	chr6:44836928-44837768	GM12878	blood:	n/a	n/a
19	ATF2	chr6:44836879-44837663	GM12878	blood:	n/a	n/a
20	ATF2	chr6:44966734-44967257	GM12878	blood:	n/a	n/a
21	ATF2	chr6:44966735-44967151	GM12878	blood:	n/a	n/a
22	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
23	BACH1	chr6:44965357-44965412	K562	blood:	n/a	n/a
24	BATF	chr6:44966783-44967196	GM12878	blood:	n/a	n/a
25	BATF	chr6:44977286-44977716	GM12878	blood:	n/a	chr6:44977540-44977551
26	BATF	chr6:44977334-44977648	GM12878	blood:	n/a	chr6:44977540-44977551
27	BATF	chr6:44947204-44947474	GM12878	blood:	n/a	n/a
28	BATF	chr6:44966841-44967148	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:44836957-44837650	GM12878	blood:	n/a	n/a
30	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
31	BHLHE40	chr6:44836956-44837694	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
34	BHLHE40	chr6:44969459-44969727	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:45016926-45017297	K562	blood:	n/a	n/a
36	BHLHE40	chr6:44888678-44889228	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:44891304-44891474	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:45011813-45011861	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr6:44889457-44889879	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
41	CBX3	chr6:44940388-44940854	K562	blood:	n/a	n/a
42	CBX3	chr6:45016920-45017304	K562	blood:	n/a	n/a
43	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
44	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
45	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
46	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
47	CBX3	chr6:44940439-44940814	K562	blood:	n/a	n/a
48	CCNT2	chr6:44888713-44888911	K562	blood:	n/a	chr6:44888832-44888852
49	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a
50	CCNT2	chr6:44893177-44893452	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44866054-44866104	NHBE	bronchial:	n/a
2	chr6:45030454-45030504	CMK	blood:	n/a
3	chr6:45030454-45030504	IMR90	lung:	fetal
4	chr6:44866054-44866104	HIPEpiC	eye:	n/a
5	chr6:45030454-45030504	GM12878	blood:	n/a
6	chr6:45030454-45030504	HCF	heart:	n/a
7	chr6:44838538-44838588	PFSK-1	brain:	n/a
8	chr6:45030454-45030504	AoSMC	blood vessel:	n/a
9	chr6:45030454-45030504	ProgFib	skin:	n/a
10	chr6:44866054-44866104	CMK	blood:	n/a
11	chr6:44838538-44838588	BJ	skin:	n/a
12	chr6:44866054-44866104	AG10803	skin:	n/a
13	chr6:44866054-44866104	RPTEC	kidney:	n/a
14	chr6:44838538-44838588	IMR90	lung:	fetal
15	chr6:45030454-45030504	HAEpiC	amniotic membrane:	n/a
16	chr6:44838538-44838588	GM06990	blood:	n/a
17	chr6:44866054-44866104	BJ	skin:	n/a
18	chr6:45030454-45030504	RPTEC	kidney:	n/a
19	chr6:44838538-44838588	HRCEpiC	kidney:	n/a
20	chr6:44866054-44866104	LNCaP	prostate:	n/a
21	chr6:45030454-45030504	AG10803	skin:	n/a
22	chr6:44866054-44866104	NT2-D1	testis:	n/a
23	chr6:44838538-44838588	PANC-1	pancreas:	n/a
24	chr6:45030454-45030504	GM12891	blood:	n/a
25	chr6:44866054-44866104	Hela-S3	cervix:	n/a
26	chr6:45030454-45030504	Hepatocyte	liver:	n/a
27	chr6:44838538-44838588	HCM	heart:	n/a
28	chr6:44866054-44866104	HCF	heart:	n/a
29	chr6:44866054-44866104	PFSK-1	brain:	n/a
30	chr6:44838538-44838588	HCPEpiC	choroid plexus:	n/a
31	chr6:44838538-44838588	NT2-D1	testis:	n/a
32	chr6:44866054-44866104	IMR90	lung:	fetal
33	chr6:44838538-44838588	HL-60	blood:	n/a
34	chr6:45030454-45030504	K562	blood:	n/a
35	chr6:44838538-44838588	HNPCEpiC	eye:	n/a
36	chr6:44866054-44866104	SK-N-MC	brain:	n/a
37	chr6:44838538-44838588	AoSMC	blood vessel:	n/a
38	chr6:45030454-45030504	ECC-1	luminal epithelium:	n/a
39	chr6:45030454-45030504	PrEC	prostate:	n/a
40	chr6:45030454-45030504	BJ	skin:	n/a
41	chr6:44866054-44866104	SKMC	muscle:	n/a
42	chr6:45030454-45030504	NHBE	bronchial:	n/a
43	chr6:44838538-44838588	ovcar-3	ovarian:	n/a
44	chr6:45030454-45030504	HRE	kidney:	n/a
45	chr6:44838538-44838588	AG09319	gingival:	n/a
46	chr6:44838538-44838588	HUVEC	blood vessel:	n/a
47	chr6:44838538-44838588	A549	lung:	n/a
48	chr6:45030454-45030504	HEEpiC	esophagus:	n/a
49	chr6:45030454-45030504	HUVEC	blood vessel:	n/a
50	chr6:44866054-44866104	AG04450	lung:	fetal

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:
2	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
3	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
4	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
5	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
6	chr12:48357281..48357866-chr6:45012051..45012551,2	Hela-S3	cervix:
7	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
8	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
9	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
10	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
11	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
12	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
13	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
14	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
15	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
16	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:
17	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
18	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
19	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
20	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
21	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
22	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
23	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
24	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
25	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
26	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
27	chr6:44888776..44891351-chr6:45344894..45347692,2	K562	blood:
28	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
29	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
30	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
31	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
32	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
33	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
34	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
35	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
36	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
37	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
38	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
39	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
40	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
41	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-5	chr6:44866448-44867032	NONHSAT112969

No data

Variant related genes	Relation type
SUPT3H	TF binding region
NUDT19P4	TF binding region
SUPT3H	CpG island
NUDT19P4	CpG island
ENSG00000196284	chromatin interactions
ENSG00000134291	chromatin interactions

Extended variants
information (count: 7783 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:7783 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3799977	chr6:44837356-44837357	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs376975007	chr6:44837360-44837361	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs370501673	chr6:44837406-44837407	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138170357	chr6:44837446-44837447	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531414766	chr6:44837454-44837455	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs116763100	chr6:44837467-44837468	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs114321185	chr6:44837502-44837503	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs577485741	chr6:44837505-44837506	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544864369	chr6:44837507-44837508	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs563020278	chr6:44837510-44837511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs3799978	chr6:44837532-44837533	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs548795057	chr6:44837557-44837558	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149685876	chr6:44837559-44837560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs73735235	chr6:44837562-44837563	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533599113	chr6:44837567-44837568	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528149885	chr6:44837652-44837653	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs187512094	chr6:44837653-44837654	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs571193326	chr6:44837664-44837665	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs375876958	chr6:44837668-44837669	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531886983	chr6:44837682-44837683	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs143632646	chr6:44837814-44837815	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs547373254	chr6:44837816-44837817	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs113879125	chr6:44837848-44837849	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs138739320	chr6:44837931-44837932	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs539264633	chr6:44837936-44837937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs536493961	chr6:44837981-44837982	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs554298264	chr6:44838077-44838078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374230690	chr6:44838084-44838085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193197808	chr6:44838085-44838086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558552699	chr6:44838091-44838092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547864348	chr6:44838105-44838106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556315999	chr6:44838107-44838108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185217835	chr6:44838141-44838142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544269197	chr6:44838165-44838166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371499723	chr6:44838170-44838171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574984264	chr6:44838184-44838185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542448474	chr6:44838210-44838211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560634023	chr6:44838217-44838218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528216152	chr6:44838222-44838223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114477673	chr6:44838268-44838269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370991569	chr6:44838277-44838278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190435648	chr6:44838280-44838281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558829566	chr6:44838302-44838303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374748185	chr6:44838304-44838305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532175232	chr6:44838330-44838331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58790049	chr6:44838352-44838353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550303994	chr6:44838374-44838375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569136123	chr6:44838390-44838391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs472672	chr6:44838409-44838410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs547999623	chr6:44838420-44838421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44828400-44837800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr6:44833600-44849400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr6:44836000-44838000	Flanking Active TSS	GM12878-XiMat	blood
4	chr6:44836200-44837400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:44836200-44837400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:44836200-44837400	Enhancers	Fetal Intestine Large	intestine
7	chr6:44836400-44837400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr6:44836600-44837800	Enhancers	Fetal Intestine Small	intestine
9	chr6:44836600-44838000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:44837000-44838000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:44837200-44838200	Enhancers	HepG2	liver
12	chr6:44837400-44837600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:44837400-44837800	Enhancers	Fetal Heart	heart
14	chr6:44837400-44837800	Weak transcription	Fetal Intestine Large	intestine
15	chr6:44837600-44838200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:44837800-44838200	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:44837800-44838200	Enhancers	Fetal Intestine Large	intestine
18	chr6:44838000-44838200	Enhancers	GM12878-XiMat	blood
19	chr6:44838000-44838400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:44838200-44848800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr6:44838400-44854200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:44844200-44847800	Weak transcription	Dnd41	blood
23	chr6:44845200-44847800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:44845800-44846400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:44846400-44847600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:44846400-44848000	Enhancers	HepG2	liver
27	chr6:44846600-44846800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:44846800-44847200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:44854600-44866200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:44859200-44889400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr6:44860000-44860600	Enhancers	Right Ventricle	heart
32	chr6:44860000-44860800	Enhancers	Fetal Brain Male	brain
33	chr6:44860000-44860800	Enhancers	Fetal Heart	heart
34	chr6:44860800-44862800	Weak transcription	Fetal Heart	heart
35	chr6:44862600-44889400	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr6:44862800-44863600	Enhancers	Fetal Heart	heart
37	chr6:44863000-44865600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr6:44863200-44866600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:44863600-44870400	Weak transcription	Aorta	Aorta
40	chr6:44864000-44866600	Enhancers	Fetal Lung	lung
41	chr6:44864200-44866600	Enhancers	Fetal Stomach	stomach
42	chr6:44864800-44888400	Weak transcription	Primary T cells from cord blood	blood
43	chr6:44865000-44865800	Weak transcription	HSMM	muscle
44	chr6:44865800-44866200	Genic enhancers	HSMM	muscle
45	chr6:44866000-44866200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:44866000-44866600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:44866000-44866600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr6:44866000-44866600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:44866000-44866600	Enhancers	Gastric	stomach
50	chr6:44866000-44866600	Enhancers	HSMMtube	muscle

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