Variant report

Variant	esv2763287
Chromosome Location	chr2:183939173-184037893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1661)
CpG islands
(count:1345)
Chromatin interactive
region (count:118)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183943053-183943747	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183977385-183977757	K562	blood:	n/a	n/a
3	ARID3A	chr2:183988399-183989979	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:183977968-183978126	K562	blood:	n/a	n/a
5	ARID3A	chr2:184009418-184009500	K562	blood:	n/a	n/a
6	ARID3A	chr2:183988933-183990031	K562	blood:	n/a	n/a
7	ARID3A	chr2:184021991-184022497	K562	blood:	n/a	n/a
8	ARID3A	chr2:183990312-183991101	K562	blood:	n/a	n/a
9	ARID3A	chr2:184011836-184011848	K562	blood:	n/a	n/a
10	ARID3A	chr2:183943226-183944503	K562	blood:	n/a	n/a
11	ATF1	chr2:183988548-183989798	K562	blood:	n/a	n/a
12	ATF1	chr2:183958913-183958980	K562	blood:	n/a	n/a
13	ATF1	chr2:184019613-184019907	K562	blood:	n/a	n/a
14	ATF1	chr2:183943040-183944478	K562	blood:	n/a	n/a
15	ATF1	chr2:183977365-183977711	K562	blood:	n/a	n/a
16	ATF2	chr2:183958654-183959350	GM12878	blood:	n/a	n/a
17	ATF2	chr2:183958643-183959484	GM12878	blood:	n/a	n/a
18	ATF2	chr2:183988645-183989273	GM12878	blood:	n/a	n/a
19	ATF2	chr2:183988711-183989839	GM12878	blood:	n/a	n/a
20	ATF2	chr2:183943208-183943674	GM12878	blood:	n/a	n/a
21	ATF2	chr2:183988604-183989274	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr2:183943071-183943612	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr2:183988667-183989691	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr2:183943094-183943882	GM12878	blood:	n/a	n/a
25	ATF2	chr2:183989322-183989822	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr2:183988652-183989324	K562	blood:	n/a	n/a
27	ATF3	chr2:183988781-183989391	A549	lung:	n/a	n/a
28	ATF3	chr2:183988586-183989641	A549	lung:	n/a	n/a
29	BACH1	chr2:183970245-183970405	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr2:183977993-183978041	K562	blood:	n/a	n/a
31	BATF	chr2:183952885-183953101	GM12878	blood:	n/a	n/a
32	BATF	chr2:183958908-183959250	GM12878	blood:	n/a	chr2:183959034-183959045 chr2:183959035-183959045
33	BATF	chr2:183989459-183989903	GM12878	blood:	n/a	n/a
34	BATF	chr2:183958806-183959262	GM12878	blood:	n/a	chr2:183959034-183959045 chr2:183959035-183959045
35	BCL11A	chr2:183958882-183959206	GM12878	blood:	n/a	chr2:183959033-183959042 chr2:183959034-183959043
36	BCL3	chr2:183988569-183989937	A549	lung:	n/a	n/a
37	BCL3	chr2:183988433-183989951	A549	lung:	n/a	n/a
38	BCLAF1	chr2:183988851-183989956	GM12878	blood:	n/a	n/a
39	BCLAF1	chr2:183958822-183959447	GM12878	blood:	n/a	chr2:183959033-183959042 chr2:183959034-183959043
40	BHLHE40	chr2:184022092-184022187	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:183942935-183944007	K562	blood:	n/a	n/a
42	BHLHE40	chr2:183943089-183944415	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:183988768-183990091	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:183988760-183989787	HepG2	liver:	n/a	n/a
45	BHLHE40	chr2:183944264-183944483	K562	blood:	n/a	n/a
46	BHLHE40	chr2:183970227-183970519	K562	blood:	n/a	n/a
47	BHLHE40	chr2:183988338-183990089	K562	blood:	n/a	n/a
48	BHLHE40	chr2:183990490-183990973	K562	blood:	n/a	n/a
49	BRCA1	chr2:183953969-183953988	HepG2	liver:	n/a	n/a
50	BRCA1	chr2:183988798-183989217	HepG2	liver:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183988933-183988983	MCF10A-Er-Src	breast:	n/a
2	chr2:183943203-183943253	RPTEC	kidney:	n/a
3	chr2:183943203-183943253	BJ	skin:	n/a
4	chr2:183988933-183988983	MCF10A-Er-Src	breast:	n/a
5	chr2:183943203-183943253	RPTEC	kidney:	n/a
6	chr2:183943203-183943253	BJ	skin:	n/a
7	chr2:183943388-183943438	NH-A	brain:	n/a
8	chr2:183943496-183943546	NHBE	bronchial:	n/a
9	chr2:183963421-183963471	PFSK-1	brain:	n/a
10	chr2:183988968-183989018	MCF10A-Er-Src	breast:	n/a
11	chr2:183943203-183943253	BE2_C	brain:	n/a
12	chr2:183943203-183943253	AG10803	skin:	n/a
13	chr2:183988968-183989018	CMK	blood:	n/a
14	chr2:183988872-183988922	RPTEC	kidney:	n/a
15	chr2:183943203-183943253	HIPEpiC	eye:	n/a
16	chr2:183963421-183963471	SAEC	small airway:	n/a
17	chr2:183943496-183943546	HRPEpiC	eye:	n/a
18	chr2:183989067-183989117	Hela-S3	cervix:	n/a
19	chr2:183943198-183943248	ovcar-3	ovarian:	n/a
20	chr2:183989067-183989117	NH-A	brain:	n/a
21	chr2:183943388-183943438	Hepatocyte	liver:	n/a
22	chr2:183943203-183943253	HUVEC	blood vessel:	n/a
23	chr2:183988960-183989010	HAEpiC	amniotic membrane:	n/a
24	chr2:183989548-183989598	PANC-1	pancreas:	n/a
25	chr2:183943469-183943519	HL-60	blood:	n/a
26	chr2:183942982-183943032	PFSK-1	brain:	n/a
27	chr2:183943938-183943988	AG10803	skin:	n/a
28	chr2:183989548-183989598	HAEpiC	amniotic membrane:	n/a
29	chr2:183943469-183943519	GM19239	blood:	n/a
30	chr2:183988872-183988922	AG09309	skin:	n/a
31	chr2:183943551-183943601	GM12891	blood:	n/a
32	chr2:183988000-183988050	HL-60	blood:	n/a
33	chr2:183943506-183943556	HL-60	blood:	n/a
34	chr2:183989047-183989097	AG09319	gingival:	n/a
35	chr2:183989047-183989097	PANC-1	pancreas:	n/a
36	chr2:183943203-183943253	AG09319	gingival:	n/a
37	chr2:183989548-183989598	HL-60	blood:	n/a
38	chr2:183943551-183943601	Caco-2	colon:	n/a
39	chr2:183943203-183943253	HCF	heart:	n/a
40	chr2:183943203-183943253	GM12891	blood:	n/a
41	chr2:183989107-183989157	HCPEpiC	choroid plexus:	n/a
42	chr2:183943388-183943438	ProgFib	skin:	n/a
43	chr2:183943203-183943253	SKMC	muscle:	n/a
44	chr2:183989107-183989157	LNCaP	prostate:	n/a
45	chr2:183989107-183989157	GM06990	blood:	n/a
46	chr2:183988933-183988983	GM06990	blood:	n/a
47	chr2:183989067-183989117	GM12892	blood:	n/a
48	chr2:183943203-183943253	ProgFib	skin:	n/a
49	chr2:183988872-183988922	AoSMC	blood vessel:	n/a
50	chr2:183943198-183943248	NHBE	bronchial:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:184015191..184017995-chr2:184020754..184023549,2	K562	blood:
2	chr2:183943480..183947089-chr2:183947127..183951235,3	MCF-7	breast:
3	chr2:184020158..184022833-chr2:184025922..184028556,2	K562	blood:
4	chr2:183941058..183944169-chr2:183988077..183990587,3	MCF-7	breast:
5	chr2:183950455..183953323-chr2:183953411..183955359,2	K562	blood:
6	chr2:183977930..183980927-chr2:183984054..183985620,2	MCF-7	breast:
7	chr2:183989189..183990903-chr2:184002119..184004777,2	MCF-7	breast:
8	chr2:184002655..184004806-chr2:184014352..184016566,2	K562	blood:
9	chr2:183988409..183991229-chr2:184005605..184009543,5	MCF-7	breast:
10	chr2:183961564..183963218-chr2:183968375..183970375,2	K562	blood:
11	chr2:183601411..183603904-chr2:183956963..183959592,2	MCF-7	breast:
12	chr2:183981717..183985228-chr2:183986533..183989454,4	MCF-7	breast:
13	chr2:183902000..183906390-chr2:183941845..183945087,6	MCF-7	breast:
14	chr2:183970085..183972201-chr2:183987942..183989595,2	MCF-7	breast:
15	chr2:183994056..183995638-chr2:184003260..184004880,2	K562	blood:
16	chr2:183981717..183985228-chr2:183986533..183989454,4	MCF-7	breast:
17	chr2:183988048..183989640-chr2:184013730..184015754,3	K562	blood:
18	chr2:183939801..183941684-chr2:183944000..183946021,2	K562	blood:
19	chr2:183975767..183977523-chr2:183982555..183984134,2	K562	blood:
20	chr2:183942606..183944610-chr2:183988840..183990429,2	K562	blood:
21	chr2:184015191..184017995-chr2:184020754..184023549,2	K562	blood:
22	chr2:183886816..183889401-chr2:183988651..183990376,2	K562	blood:
23	chr2:183942911..183945636-chr2:183991182..183993608,2	K562	blood:
24	chr2:183973630..183975717-chr2:183987994..183990316,2	K562	blood:
25	chr2:183943535..183946309-chr2:183948894..183950555,3	K562	blood:
26	chr2:183935971..183937541-chr2:183938769..183940980,2	K562	blood:
27	chr2:183987752..183989755-chr2:184035957..184037928,2	MCF-7	breast:
28	chr2:183988386..183990737-chr2:184027696..184029728,3	K562	blood:
29	chr2:183954410..183956747-chr2:183990297..183991914,2	K562	blood:
30	chr2:184018781..184021679-chr2:184025666..184028556,3	K562	blood:
31	chr2:183936424..183941841-chr2:183941943..183946520,8	K562	blood:
32	chr2:183976023..183978343-chr2:183982634..183984997,2	K562	blood:
33	chr2:184006368..184007873-chr2:184008611..184010923,2	MCF-7	breast:
34	chr2:183976023..183978343-chr2:183982634..183984997,2	K562	blood:
35	chr2:183998810..184000982-chr2:184027517..184029612,2	K562	blood:
36	chr2:184000064..184001821-chr2:184013911..184016128,2	MCF-7	breast:
37	chr2:183987113..183989914-chr2:184001624..184005072,5	K562	blood:
38	chr2:184007568..184011382-chr2:184012317..184014101,3	K562	blood:
39	chr2:183937263..183939244-chr2:183999975..184002800,2	K562	blood:
40	chr2:183937263..183939244-chr2:183999975..184002800,2	K562	blood:
41	chr2:183989265..183990800-chr2:184010673..184012208,2	MCF-7	breast:
42	chr2:183895298..183904606-chr2:183986062..183992067,16	K562	blood:
43	chr2:184005599..184007720-chr2:184007957..184009877,2	K562	blood:
44	chr2:183989265..183990800-chr2:184010673..184012208,2	MCF-7	breast:
45	chr2:183775532..183777640-chr2:183990491..183993127,2	K562	blood:
46	chr2:183900414..183906188-chr2:183987961..183990917,10	MCF-7	breast:
47	chr2:183992197..183994349-chr2:184006346..184008645,2	K562	blood:
48	chr2:183990685..183993122-chr2:184003291..184005876,2	K562	blood:
49	chr2:184005599..184007720-chr2:184007957..184009877,2	K562	blood:
50	chr2:183902872..183905490-chr2:183940905..183944482,4	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DUSP19-1	chr2:183983319-183983667	NONHSAT075936
2	lnc-NCKAP1-1	chr2:183973168-183973247	ENSG00000224643.1
3	lnc-DUSP19-1	chr2:183984734-183984790	NONHSAT075936
4	lnc-DUSP19-1	chr2:183983319-183983470	XLOC_001778
5	lnc-NCKAP1-1	chr2:183972220-183972431	ENSG00000224643.1
6	lnc-NCKAP1-1	chr2:183948133-183948267	ENSG00000224643.1
7	lnc-DUSP19-1	chr2:183982247-183982354	NONHSAT075936
8	lnc-DUSP19-1	chr2:183982268-183982354	XLOC_001778

No data

Variant related genes	Relation type
KRT8P10	TF binding region
DUSP19	TF binding region
NUP35	TF binding region
ENSG00000224643	TF binding region
KRT8P10	CpG island
DUSP19	CpG island
NUP35	CpG island
ENSG00000224643	CpG island
ENSG00000138434	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000162999	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000163002	chromatin interactions
ENSG00000202141	chromatin interactions
ENSG00000161960	chromatin interactions
ENSG00000231203	chromatin interactions

Extended variants
information (count: 3929 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:3929 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4666885	chr2:183939173-183939174	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530785423	chr2:183939180-183939181	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144050482	chr2:183939191-183939192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs189236044	chr2:183939200-183939201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148654893	chr2:183939218-183939219	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs546743809	chr2:183939246-183939247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566566515	chr2:183939316-183939317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375471371	chr2:183939340-183939341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142230832	chr2:183939352-183939353	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs16823967	chr2:183939361-183939362	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs146764015	chr2:183939368-183939369	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571591035	chr2:183939375-183939376	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372675079	chr2:183939387-183939388	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537717159	chr2:183939388-183939389	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534042083	chr2:183939410-183939411	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567353486	chr2:183939433-183939434	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs536243348	chr2:183939443-183939444	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs553092411	chr2:183939459-183939460	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs373757629	chr2:183939460-183939461	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs572963157	chr2:183939462-183939463	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs192860596	chr2:183939492-183939493	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs75727280	chr2:183939498-183939499	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs543885742	chr2:183939524-183939525	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs575462860	chr2:183939617-183939618	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs17704284	chr2:183939618-183939619	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs561144471	chr2:183939648-183939649	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs140384648	chr2:183939662-183939663	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184787276	chr2:183939720-183939721	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs144229446	chr2:183939723-183939724	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs72890345	chr2:183939724-183939725	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138771511	chr2:183939761-183939762	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs189029384	chr2:183939791-183939792	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs75474658	chr2:183939792-183939793	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs146545698	chr2:183939815-183939816	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs550910369	chr2:183939836-183939837	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs181750509	chr2:183939837-183939838	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs536256805	chr2:183939893-183939894	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs552904408	chr2:183939992-183939993	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs566872793	chr2:183939994-183939995	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs539087589	chr2:183939996-183939997	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs373853213	chr2:183939998-183939999	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs558766271	chr2:183940001-183940002	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs556024986	chr2:183940002-183940003	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs575424207	chr2:183940075-183940076	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs559920638	chr2:183940144-183940145	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576045827	chr2:183940187-183940188	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs141299410	chr2:183940229-183940230	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs115734647	chr2:183940236-183940237	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs568723791	chr2:183940304-183940305	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs186365675	chr2:183940350-183940351	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183934800-183943000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:183934800-183943000	Weak transcription	Esophagus	oesophagus
3	chr2:183934800-183943000	Weak transcription	Right Atrium	heart
4	chr2:183935800-183943000	Weak transcription	Aorta	Aorta
5	chr2:183936400-183940200	Weak transcription	Gastric	stomach
6	chr2:183936400-183943000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:183936400-183943000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:183940200-183940800	Enhancers	Gastric	stomach
9	chr2:183940200-183940800	Enhancers	K562	blood
10	chr2:183940600-183940800	Enhancers	Brain Substantia Nigra	brain
11	chr2:183940800-183941600	Enhancers	Stomach Mucosa	stomach
12	chr2:183940800-183942800	Weak transcription	K562	blood
13	chr2:183940800-183943000	Weak transcription	Gastric	stomach
14	chr2:183941000-183942800	Weak transcription	Brain Substantia Nigra	brain
15	chr2:183941600-183942000	Weak transcription	Stomach Mucosa	stomach
16	chr2:183942000-183942200	Enhancers	Stomach Mucosa	stomach
17	chr2:183942200-183942800	Bivalent Enhancer	HepG2	liver
18	chr2:183942200-183943000	Weak transcription	Stomach Mucosa	stomach
19	chr2:183942200-183943000	Enhancers	Thymus	Thymus
20	chr2:183942600-183942800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr2:183942600-183944400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:183942800-183943000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
23	chr2:183942800-183943000	Active TSS	Primary hematopoietic stem cells	blood
24	chr2:183942800-183943000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:183942800-183943000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr2:183942800-183943000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr2:183942800-183943000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr2:183942800-183943000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:183942800-183943000	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr2:183942800-183943200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr2:183942800-183943200	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr2:183942800-183943400	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr2:183942800-183943400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:183942800-183943400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:183942800-183943600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:183942800-183943600	Active TSS	Liver	Liver
37	chr2:183942800-183943800	Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr2:183942800-183943800	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr2:183942800-183943800	Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr2:183942800-183943800	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr2:183942800-183943800	Active TSS	NH-A	brain
42	chr2:183942800-183944000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:183942800-183944000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:183942800-183944000	Bivalent/Poised TSS	HepG2	liver
45	chr2:183942800-183944000	Active TSS	NHEK	skin
46	chr2:183942800-183944200	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr2:183942800-183944200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:183942800-183944200	Active TSS	Muscle Satellite Cultured Cells	--
49	chr2:183942800-183944200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr2:183942800-183944200	Active TSS	Brain Germinal Matrix	brain

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