Variant report

Variant	nsv1001555
Chromosome Location	chr2:125904415-126630781
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2271)
CpG islands
(count:244)
Chromatin interactive
region (count:41)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2271 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:125926516-125927003	GM12878	blood:	n/a	n/a
2	ATF2	chr2:126156277-126156950	GM12878	blood:	n/a	n/a
3	ATF2	chr2:126155295-126156152	GM12878	blood:	n/a	n/a
4	ATF2	chr2:125926631-125926967	GM12878	blood:	n/a	n/a
5	ATF2	chr2:125924680-125925234	GM12878	blood:	n/a	n/a
6	ATF2	chr2:126156222-126157393	GM12878	blood:	n/a	n/a
7	ATF2	chr2:126316690-126317178	GM12878	blood:	n/a	n/a
8	ATF2	chr2:126400678-126401617	GM12878	blood:	n/a	n/a
9	ATF2	chr2:126155036-126156050	GM12878	blood:	n/a	n/a
10	BACH1	chr2:126458688-126458954	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:126458745-126458939	K562	blood:	n/a	n/a
12	BACH1	chr2:126353854-126354004	K562	blood:	n/a	n/a
13	BATF	chr2:126088857-126089078	GM12878	blood:	n/a	n/a
14	BATF	chr2:126492832-126493048	GM12878	blood:	n/a	n/a
15	BATF	chr2:126316692-126317146	GM12878	blood:	n/a	n/a
16	BATF	chr2:126155442-126155871	GM12878	blood:	n/a	n/a
17	BATF	chr2:126155425-126155912	GM12878	blood:	n/a	n/a
18	BATF	chr2:126401281-126401587	GM12878	blood:	n/a	n/a
19	BATF	chr2:126156294-126156689	GM12878	blood:	n/a	n/a
20	BATF	chr2:126081942-126082216	GM12878	blood:	n/a	n/a
21	BATF	chr2:126316741-126317078	GM12878	blood:	n/a	n/a
22	BATF	chr2:126237134-126237359	GM12878	blood:	n/a	n/a
23	BATF	chr2:126401292-126401608	GM12878	blood:	n/a	n/a
24	BATF	chr2:126212687-126213029	GM12878	blood:	n/a	n/a
25	BATF	chr2:125924684-125925219	GM12878	blood:	n/a	n/a
26	BATF	chr2:126416133-126416550	GM12878	blood:	n/a	chr2:126416326-126416337
27	BATF	chr2:126087822-126088016	GM12878	blood:	n/a	n/a
28	BATF	chr2:126503224-126503450	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:126155449-126155921	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:126155560-126155740	GM12878	blood:	n/a	n/a
31	BCL3	chr2:126088801-126089122	GM12878	blood:	n/a	n/a
32	BCL3	chr2:126155574-126155960	GM12878	blood:	n/a	n/a
33	BCL3	chr2:126156313-126156789	GM12878	blood:	n/a	n/a
34	BCL3	chr2:125924759-125925157	GM12878	blood:	n/a	n/a
35	BCL3	chr2:126155182-126156009	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:126155332-126155937	GM12878	blood:	n/a	n/a
37	BCLAF1	chr2:126155048-126155978	GM12878	blood:	n/a	n/a
38	BCLAF1	chr2:126401122-126401620	GM12878	blood:	n/a	n/a
39	BCLAF1	chr2:126016959-126017405	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:125985580-125985619	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:126229714-126229879	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:126504323-126504523	GM12878	blood:	n/a	n/a
43	BHLHE40	chr2:126541287-126541503	K562	blood:	n/a	n/a
44	BHLHE40	chr2:126568769-126569122	K562	blood:	n/a	n/a
45	BHLHE40	chr2:126155240-126155918	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:126000266-126000306	GM12878	blood:	n/a	n/a
47	BHLHE40	chr2:126087765-126088070	GM12878	blood:	n/a	n/a
48	BRCA1	chr2:126155630-126155633	GM12878	blood:	n/a	n/a
49	BRCA1	chr2:126503179-126503329	HepG2	liver:	n/a	n/a
50	CCNT2	chr2:125999661-125999834	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:126504079-126504129	GM06990	blood:	n/a
2	chr2:126504079-126504129	HEEpiC	esophagus:	n/a
3	chr2:126595338-126595388	A549	lung:	n/a
4	chr2:126350052-126350102	K562	blood:	n/a
5	chr2:126235913-126235963	HCPEpiC	choroid plexus:	n/a
6	chr2:126350052-126350102	HCT-116	colon:	n/a
7	chr2:126235913-126235963	Caco-2	colon:	n/a
8	chr2:126595338-126595388	AG04449	skin:	fetal
9	chr2:126235913-126235963	HRCEpiC	kidney:	n/a
10	chr2:126504079-126504129	BJ	skin:	n/a
11	chr2:126350052-126350102	HL-60	blood:	n/a
12	chr2:126350052-126350102	BE2_C	brain:	n/a
13	chr2:126350052-126350102	SK-N-MC	brain:	n/a
14	chr2:126595338-126595388	T-47D	breast:	n/a
15	chr2:126504079-126504129	HRE	kidney:	n/a
16	chr2:126595338-126595388	AG04450	lung:	fetal
17	chr2:126235913-126235963	PFSK-1	brain:	n/a
18	chr2:126595338-126595388	IMR90	lung:	fetal
19	chr2:126504079-126504129	HNPCEpiC	eye:	n/a
20	chr2:126350052-126350102	H1-hESC	embryonic stem cell:	embryo
21	chr2:126504079-126504129	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:126504079-126504129	SK-N-MC	brain:	n/a
23	chr2:126595338-126595388	HMEC	breast:	n/a
24	chr2:126235913-126235963	SKMC	muscle:	n/a
25	chr2:126235913-126235963	AG10803	skin:	n/a
26	chr2:126504079-126504129	AG09309	skin:	n/a
27	chr2:126595338-126595388	ECC-1	luminal epithelium:	n/a
28	chr2:126350052-126350102	HRCEpiC	kidney:	n/a
29	chr2:126504079-126504129	CMK	blood:	n/a
30	chr2:126595338-126595388	PrEC	prostate:	n/a
31	chr2:126504079-126504129	RPTEC	kidney:	n/a
32	chr2:126595338-126595388	SK-N-SH_RA	brain:	n/a
33	chr2:126504079-126504129	GM19239	blood:	n/a
34	chr2:126350052-126350102	HEK293	kidney:	embryo
35	chr2:126504079-126504129	AG04449	skin:	fetal
36	chr2:126504079-126504129	SAEC	small airway:	n/a
37	chr2:126235913-126235963	AG04449	skin:	fetal
38	chr2:126595338-126595388	LNCaP	prostate:	n/a
39	chr2:126235913-126235963	NT2-D1	testis:	n/a
40	chr2:126350052-126350102	GM12878	blood:	n/a
41	chr2:126235913-126235963	HCM	heart:	n/a
42	chr2:126235913-126235963	NB4	blood:	n/a
43	chr2:126350052-126350102	BJ	skin:	n/a
44	chr2:126235913-126235963	GM12892	blood:	n/a
45	chr2:126350052-126350102	LNCaP	prostate:	n/a
46	chr2:126504079-126504129	SKMC	muscle:	n/a
47	chr2:126504079-126504129	H1-hESC	embryonic stem cell:	embryo
48	chr2:126504079-126504129	HCF	heart:	n/a
49	chr2:126595338-126595388	AG09319	gingival:	n/a
50	chr2:126595338-126595388	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:125567512..125568092-chr2:126229510..126230293,2	MCF-7	breast:
2	chr2:126398778..126400895-chr2:126402290..126404652,2	K562	blood:
3	chr2:126475681..126477438-chr2:126478103..126480608,2	K562	blood:
4	chr2:126480919..126482425-chr2:126537842..126540403,2	K562	blood:
5	chr2:126159691..126161842-chr2:126162114..126163675,2	MCF-7	breast:
6	chr2:126441149..126442866-chr2:126450432..126451944,2	K562	blood:
7	chr2:126576985..126578529-chr2:126578759..126580981,2	K562	blood:
8	chr2:126195917..126197437-chr21:34914470..34917100,2	MCF-7	breast:
9	chr2:126480919..126482425-chr2:126537842..126540403,2	K562	blood:
10	chr2:126398778..126400895-chr2:126402290..126404652,2	K562	blood:
11	chr2:126423393..126427272-chr2:126428665..126431892,3	K562	blood:
12	chr2:126503076..126503791-chr2:127534683..127535324,4	MCF-7	breast:
13	chr2:126047722..126049606-chr2:126299311..126300955,2	K562	blood:
14	chr2:126210559..126213448-chr2:126214193..126215952,2	MCF-7	breast:
15	chr2:126042769..126044618-chr2:126044851..126047472,2	K562	blood:
16	chr2:126475681..126477438-chr2:126478103..126480608,2	K562	blood:
17	chr2:126165207..126167120-chr2:126171074..126173153,2	K562	blood:
18	chr2:126503200..126503743-chr2:127729269..127730019,3	MCF-7	breast:
19	chr2:126324067..126325943-chr2:126329563..126331533,2	K562	blood:
20	chr2:126159691..126161842-chr2:126162114..126163675,2	MCF-7	breast:
21	chr2:126601742..126603479-chr2:126606916..126609588,2	K562	blood:
22	chr2:126601742..126603479-chr2:126606916..126609588,2	K562	blood:
23	chr2:122288312..122291056-chr2:126544098..126546696,2	K562	blood:
24	chr2:126423393..126427272-chr2:126428665..126431892,3	K562	blood:
25	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
26	chr2:126441149..126442866-chr2:126450432..126451944,2	K562	blood:
27	chr2:126413571..126415580-chr2:126417629..126419546,2	K562	blood:
28	chr2:126047722..126049606-chr2:126299311..126300955,2	K562	blood:
29	chr2:126502797..126503723-chr2:127002290..127003108,2	MCF-7	breast:
30	chr2:126441721..126443799-chr2:126451980..126453632,2	K562	blood:
31	chr2:126412945..126415071-chr2:126417219..126419546,2	K562	blood:
32	chr2:126210559..126213448-chr2:126214193..126215952,2	MCF-7	breast:
33	chr2:126574297..126576211-chr2:126580943..126583873,2	K562	blood:
34	chr2:126413571..126415580-chr2:126417629..126419546,2	K562	blood:
35	chr2:126441721..126443799-chr2:126451980..126453632,2	K562	blood:
36	chr2:126165207..126167120-chr2:126171074..126173153,2	K562	blood:
37	chr2:126042769..126044618-chr2:126044851..126047472,2	K562	blood:
38	chr2:126324067..126325943-chr2:126329563..126331533,2	K562	blood:
39	chr2:126412945..126415071-chr2:126417219..126419546,2	K562	blood:
40	chr2:126574297..126576211-chr2:126580943..126583873,2	K562	blood:
41	chr2:126502767..126504184-chr2:127534751..127535559,5	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BIN1-3	chr2:126464386-126464754	NONHSAT074119
2	lnc-BIN1-3	chr2:126483361-126483468	NONHSAT074119
3	lnc-CNTNAP5-2	chr2:126474462-126474592	NONHSAT074117
4	lnc-CNTNAP5-3	chr2:126468546-126468947	XLOC_001657
5	lnc-CNTNAP5-2	chr2:126456152-126456276	NONHSAT074117
6	lnc-CNTNAP5-3	chr2:126523154-126523419	XLOC_001657
7	lnc-BIN1-3	chr2:126464387-126464754	XLOC_002307
8	lnc-CNTNAP5-2	chr2:126457983-126458113	FPKM1_group_17139_transcript_1
9	lnc-BIN1-9	chr2:126199832-126199992	l_1943_chr2:126180856-126199888_testes
10	lnc-GYPC-3	chr2:126591970-126592032	NONHSAT074124
11	lnc-GYPC-3	chr2:126584146-126584357	NONHSAT074124
12	lnc-GYPC-4	chr2:126580685-126580892	NONHSAT074123
13	lnc-CNTNAP5-9	chr2:126185016-126185417	NONHSAT074116
14	lnc-BIN1-9	chr2:126180857-126181224	l_1943_chr2:126180856-126199888_testes
15	lnc-CNTNAP5-2	chr2:126456152-126456276	FPKM1_group_17139_transcript_1
16	lnc-GYPC-3	chr2:126586980-126587217	NONHSAT074124
17	lnc-GYPC-3	chr2:126588064-126588174	NONHSAT074124
18	lnc-BIN1-3	chr2:126483362-126483468	XLOC_002307
19	lnc-CNTNAP5-3	chr2:126468545-126468947	NONHSAT074121
20	lnc-CNTNAP5-9	chr2:126239624-126239889	NONHSAT074116
21	lnc-CNTNAP5-3	chr2:126523153-126523419	NONHSAT074121

No data

Variant related genes	Relation type
ENSG00000235491	TF binding region
ENSG00000224410	TF binding region
ENSG00000235491	CpG island
ENSG00000224410	CpG island
ENSG00000159131	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000224410	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000159140	chromatin interactions
KCNC4	miRNA target sites
KCNH8	miRNA target sites

Extended variants
information (count: 9312 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:9312 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202178597	chr2:125924201-125924202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138939149	chr2:125924214-125924215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181951165	chr2:125924227-125924228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374412553	chr2:125924229-125924230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12999049	chr2:125924242-125924243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566332134	chr2:125924246-125924247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561765945	chr2:125924263-125924264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185250948	chr2:125924291-125924292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139204344	chr2:125924308-125924309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188112083	chr2:125924334-125924335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs13004238	chr2:125924362-125924363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143215458	chr2:125924423-125924424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552378750	chr2:125924449-125924450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4438483	chr2:125924509-125924510	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147529182	chr2:125924598-125924599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548476858	chr2:125924725-125924726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181305238	chr2:125924752-125924753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113681427	chr2:125924759-125924760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570153270	chr2:125924781-125924782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537174449	chr2:125924796-125924797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533515296	chr2:125924803-125924804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12711702	chr2:125924841-125924842	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537490014	chr2:125924843-125924844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140210304	chr2:125925005-125925006	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556352528	chr2:125925059-125925060	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185379201	chr2:125925088-125925089	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142028346	chr2:125925104-125925105	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565215740	chr2:125925126-125925127	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191057768	chr2:125925141-125925142	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376741963	chr2:125925221-125925222	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369831171	chr2:125925328-125925329	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs376689574	chr2:125925334-125925335	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs139722992	chr2:125925335-125925336	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs541062788	chr2:125925388-125925389	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs149795471	chr2:125925394-125925395	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs183727092	chr2:125925442-125925443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186564298	chr2:125925446-125925447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543903003	chr2:125925504-125925505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192298207	chr2:125925515-125925516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558762182	chr2:125925521-125925522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548514601	chr2:125925608-125925609	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568257094	chr2:125925616-125925617	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527330400	chr2:125925643-125925644	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72967803	chr2:125925653-125925654	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551859461	chr2:125925684-125925685	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139252849	chr2:125925686-125925687	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539166660	chr2:125925696-125925697	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555791183	chr2:125925777-125925778	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537048329	chr2:125925780-125925781	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569924147	chr2:125925819-125925820	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125924200-125925000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:125924400-125925000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:125924600-125925800	Enhancers	Osteobl	bone
4	chr2:125924800-125926000	Enhancers	NHLF	lung
5	chr2:125925000-125925400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:125925000-125925400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:125925000-125925400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:125925000-125927000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:125925200-125926000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:125925200-125926000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:125925400-125925600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:125925400-125925800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:125925400-125927800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:125925600-125926200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:125925800-125927000	Flanking Active TSS	Osteobl	bone
16	chr2:125925800-125927200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:125926000-125926800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:125926200-125927000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:125926800-125927000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:125927000-125927800	Enhancers	Osteobl	bone
21	chr2:125929600-125929800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:125932600-125933400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:125932800-125933600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:125933200-125933400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:125933200-125933600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:125933200-125933600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr2:125933200-125933600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:125933600-125943400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr2:125943400-125944000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:125943400-125944000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:125943600-125944200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:125951600-125952600	Enhancers	Brain Germinal Matrix	brain
33	chr2:125951800-125952200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:125960600-125961000	Enhancers	GM12878-XiMat	blood
35	chr2:125966800-125968000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr2:125967000-125967800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:125967400-125968000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:125967400-125968000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:125967400-125968000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:125967600-125968000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:125967600-125968000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr2:125967600-125968200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:125969800-125975400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr2:125979600-125979800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:125982400-125983000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:126012000-126012800	Enhancers	Brain Germinal Matrix	brain
47	chr2:126012800-126014800	Weak transcription	Brain Germinal Matrix	brain
48	chr2:126014800-126015600	Enhancers	Brain Germinal Matrix	brain
49	chr2:126015600-126017600	Weak transcription	Brain Germinal Matrix	brain
50	chr2:126017400-126018600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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