Variant report

Variant	nsv516759
Chromosome Location	chr2:127796666-127859441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2159)
CpG islands
(count:1714)
Chromatin interactive
region (count:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:127807793-127807989	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:127822615-127822618	K562	blood:	n/a	n/a
3	ATF2	chr2:127839350-127839700	GM12878	blood:	n/a	n/a
4	ATF2	chr2:127825499-127825993	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:127797006-127797597	GM12878	blood:	n/a	n/a
6	ATF2	chr2:127825494-127825920	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:127844429-127844950	GM12878	blood:	n/a	n/a
8	ATF2	chr2:127844404-127844947	GM12878	blood:	n/a	n/a
9	ATF2	chr2:127797116-127797488	GM12878	blood:	n/a	n/a
10	ATF3	chr2:127825607-127825875	K562	blood:	n/a	n/a
11	ATF3	chr2:127822254-127822814	A549	lung:	n/a	n/a
12	ATF3	chr2:127822206-127822801	K562	blood:	n/a	n/a
13	ATF3	chr2:127822130-127822684	K562	blood:	n/a	n/a
14	ATF3	chr2:127825591-127825922	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:127825651-127825951	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:127802018-127802163	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:127822214-127822973	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:127846567-127846639	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:127822234-127822731	K562	blood:	n/a	n/a
20	BACH1	chr2:127807740-127808003	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr2:127796995-127797551	GM12878	blood:	n/a	chr2:127797302-127797313
22	BATF	chr2:127797111-127797480	GM12878	blood:	n/a	chr2:127797302-127797313
23	BATF	chr2:127822263-127822708	GM12878	blood:	n/a	chr2:127822516-127822527 chr2:127822517-127822527
24	BCL11A	chr2:127797115-127797534	GM12878	blood:	n/a	chr2:127797302-127797311 chr2:127797301-127797310
25	BCL11A	chr2:127797200-127797457	GM12878	blood:	n/a	chr2:127797302-127797311 chr2:127797301-127797310
26	BCL11A	chr2:127844549-127844858	GM12878	blood:	n/a	n/a
27	BCL3	chr2:127811506-127811950	GM12878	blood:	n/a	n/a
28	BCL3	chr2:127801129-127802418	GM12878	blood:	n/a	n/a
29	BCL3	chr2:127811578-127811877	GM12878	blood:	n/a	n/a
30	BCL3	chr2:127801087-127802446	GM12878	blood:	n/a	n/a
31	BCL3	chr2:127822265-127822701	K562	blood:	n/a	n/a
32	BCL3	chr2:127821940-127822838	A549	lung:	n/a	chr2:127822050-127822059
33	BCL3	chr2:127807664-127808252	A549	lung:	n/a	n/a
34	BCLAF1	chr2:127839268-127839716	GM12878	blood:	n/a	n/a
35	BCLAF1	chr2:127844359-127844791	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:127822259-127822834	K562	blood:	n/a	n/a
37	BCLAF1	chr2:127825630-127825900	GM12878	blood:	n/a	n/a
38	BCLAF1	chr2:127822262-127822771	K562	blood:	n/a	n/a
39	BCLAF1	chr2:127822359-127822805	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:127838526-127839961	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:127804192-127804461	HepG2	liver:	n/a	chr2:127804298-127804307
42	BHLHE40	chr2:127825347-127825940	GM12878	blood:	n/a	n/a
43	BHLHE40	chr2:127822373-127822818	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:127838100-127838398	K562	blood:	n/a	n/a
45	BHLHE40	chr2:127844445-127844936	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:127823468-127823585	K562	blood:	n/a	n/a
47	BHLHE40	chr2:127804162-127804488	K562	blood:	n/a	chr2:127804298-127804307
48	BHLHE40	chr2:127819030-127819058	HepG2	liver:	n/a	n/a
49	BHLHE40	chr2:127841796-127841981	K562	blood:	n/a	n/a
50	BHLHE40	chr2:127807725-127808031	K562	blood:	n/a	chr2:127807929-127807945

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127815206-127815256	GM12891	blood:	n/a
2	chr2:127825935-127825985	MCF10A-Er-Src	breast:	n/a
3	chr2:127841945-127841995	HCM	heart:	n/a
4	chr2:127852450-127852500	GM06990	blood:	n/a
5	chr2:127800962-127801012	Caco-2	colon:	n/a
6	chr2:127821711-127821761	ProgFib	skin:	n/a
7	chr2:127815206-127815256	GM12891	blood:	n/a
8	chr2:127825935-127825985	MCF10A-Er-Src	breast:	n/a
9	chr2:127841945-127841995	HCM	heart:	n/a
10	chr2:127852450-127852500	GM06990	blood:	n/a
11	chr2:127800962-127801012	Caco-2	colon:	n/a
12	chr2:127821711-127821761	ProgFib	skin:	n/a
13	chr2:127826149-127826199	NHBE	bronchial:	n/a
14	chr2:127801137-127801187	AoSMC	blood vessel:	n/a
15	chr2:127811853-127811903	HIPEpiC	eye:	n/a
16	chr2:127818000-127818050	IMR90	lung:	fetal
17	chr2:127805855-127805905	BE2_C	brain:	n/a
18	chr2:127801271-127801321	Hepatocyte	liver:	n/a
19	chr2:127821711-127821761	Jurkat	blood:	n/a
20	chr2:127821711-127821761	PFSK-1	brain:	n/a
21	chr2:127852450-127852500	AoSMC	blood vessel:	n/a
22	chr2:127818046-127818096	AG09319	gingival:	n/a
23	chr2:127801137-127801187	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:127841945-127841995	AG09319	gingival:	n/a
25	chr2:127818101-127818151	Caco-2	colon:	n/a
26	chr2:127805855-127805905	AG10803	skin:	n/a
27	chr2:127805910-127805960	SK-N-SH	brain:	n/a
28	chr2:127825935-127825985	H1-hESC	embryonic stem cell:	embryo
29	chr2:127800646-127800696	HRPEpiC	eye:	n/a
30	chr2:127839539-127839589	NHBE	bronchial:	n/a
31	chr2:127811853-127811903	ovcar-3	ovarian:	n/a
32	chr2:127805770-127805820	BE2_C	brain:	n/a
33	chr2:127811805-127811855	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:127811805-127811855	GM12878	blood:	n/a
35	chr2:127815133-127815183	AG04449	skin:	fetal
36	chr2:127800646-127800696	IMR90	lung:	fetal
37	chr2:127830703-127830753	Jurkat	blood:	n/a
38	chr2:127800646-127800696	GM12891	blood:	n/a
39	chr2:127852450-127852500	GM12878	blood:	n/a
40	chr2:127805855-127805905	SK-N-SH_RA	brain:	n/a
41	chr2:127815206-127815256	SK-N-SH_RA	brain:	n/a
42	chr2:127830703-127830753	HepG2	liver:	n/a
43	chr2:127818226-127818276	K562	blood:	n/a
44	chr2:127818000-127818050	NHBE	bronchial:	n/a
45	chr2:127818101-127818151	NHDF-neo	bronchial:	n/a
46	chr2:127818000-127818050	HL-60	blood:	n/a
47	chr2:127801271-127801321	K562	blood:	n/a
48	chr2:127815133-127815183	HEEpiC	esophagus:	n/a
49	chr2:127819455-127819505	ovcar-3	ovarian:	n/a
50	chr2:127839539-127839589	BJ	skin:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:127825712..127826261-chr2:127901784..127902300,2	MCF-7	breast:
2	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
3	chr2:127852372..127854342-chr2:127858358..127859956,2	MCF-7	breast:
4	chr2:127809898..127812598-chr2:127812721..127816309,3	MCF-7	breast:
5	chr2:127823166..127825424-chr2:127856557..127859034,2	MCF-7	breast:
6	chr2:127843180..127845570-chr2:127848864..127852714,3	MCF-7	breast:
7	chr2:127825651..127827427-chr2:127830304..127832432,2	MCF-7	breast:
8	chr2:127800876..127803938-chr2:127806149..127808710,3	MCF-7	breast:
9	chr2:127837345..127839578-chr2:127840445..127843454,3	MCF-7	breast:
10	chr2:127818892..127820837-chr2:127828429..127830167,2	MCF-7	breast:
11	chr2:127834991..127836623-chr2:127840456..127842151,2	MCF-7	breast:
12	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
13	chr2:127837291..127839948-chr2:127841422..127844629,3	K562	blood:
14	chr2:127834701..127837421-chr2:127840734..127842424,2	MCF-7	breast:
15	chr2:127854702..127856656-chr2:127856950..127858701,2	MCF-7	breast:
16	chr2:127808007..127810886-chr2:127814452..127816219,3	K562	blood:
17	chr2:127840959..127842662-chr2:127845324..127846999,2	K562	blood:
18	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
19	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
20	chr2:127825651..127827427-chr2:127830304..127832432,2	MCF-7	breast:
21	chr2:127810346..127812900-chr2:127820941..127823666,3	MCF-7	breast:
22	chr2:127815185..127819090-chr2:127820939..127825042,7	K562	blood:
23	chr2:127002328..127003186-chr2:127807433..127808421,2	K562	blood:
24	chr2:127818892..127820837-chr2:127828429..127830167,2	MCF-7	breast:
25	chr2:127782007..127782956-chr2:127806151..127807307,3	MCF-7	breast:
26	chr2:127857696..127862567-chr2:127862895..127866178,8	MCF-7	breast:
27	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
28	chr2:127813553..127815177-chr2:127820446..127822528,2	MCF-7	breast:
29	chr2:127853337..127855770-chr2:127871735..127873345,2	K562	blood:
30	chr2:127829702..127832406-chr2:127833096..127835380,2	K562	blood:
31	chr2:127805679..127808550-chr2:127820998..127823785,2	MCF-7	breast:
32	chr2:127822672..127825565-chr2:127830790..127832845,2	K562	blood:
33	chr2:127808007..127810886-chr2:127814452..127816219,3	K562	blood:
34	chr2:127822672..127825565-chr2:127830790..127832845,2	K562	blood:
35	chr2:127825705..127826883-chr2:127897059..127898198,8	MCF-7	breast:
36	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
37	chr2:127854702..127856656-chr2:127856950..127858701,2	MCF-7	breast:
38	chr2:127815347..127818543-chr2:127821043..127823308,3	K562	blood:
39	chr2:127844458..127846446-chr2:127850246..127851813,2	K562	blood:
40	chr2:127846711..127850055-chr2:127853164..127855548,3	MCF-7	breast:
41	chr2:127812299..127814743-chr2:127815692..127817435,2	MCF-7	breast:
42	chr2:127822177..127823094-chr7:128694437..128695276,2	Hela-S3	cervix:
43	chr2:127839430..127842816-chr2:127848432..127852029,4	MCF-7	breast:
44	chr2:127852372..127854342-chr2:127858358..127859956,2	MCF-7	breast:
45	chr2:127643679..127644563-chr2:127807789..127808402,4	MCF-7	breast:
46	chr2:127840959..127842662-chr2:127845324..127846999,2	K562	blood:
47	chr2:127643808..127644560-chr2:127807706..127808371,2	K562	blood:
48	chr2:127824897..127826990-chr2:127827722..127829890,2	K562	blood:
49	chr2:127829446..127832299-chr2:127837118..127839537,2	K562	blood:
50	chr2:127822075..127822831-chr2:128145042..128145699,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
BIN1	TF binding region
BIN1	CpG island
ENSG00000260163	chromatin interactions
ENSG00000136717	chromatin interactions
ENSG00000260634	chromatin interactions
ENSG00000169967	chromatin interactions
ENSG00000064419	chromatin interactions

Extended variants
information (count: 2892 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2892 , 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	rs17014788	chr2:127796666-127796667	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575887106	chr2:127796716-127796717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188298355	chr2:127796723-127796724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547062762	chr2:127796784-127796785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561723924	chr2:127796788-127796789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181852209	chr2:127796789-127796790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565950744	chr2:127796791-127796792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57430631	chr2:127796797-127796798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184859243	chr2:127796804-127796805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560544842	chr2:127796819-127796820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372644588	chr2:127796847-127796848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552567161	chr2:127796879-127796880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188746533	chr2:127796891-127796892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547584376	chr2:127796901-127796902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375987288	chr2:127796950-127796951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548902042	chr2:127796982-127796983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547813332	chr2:127796985-127796986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34558712	chr2:127796986-127796987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568542782	chr2:127796997-127796998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181745393	chr2:127797012-127797013	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs541228832	chr2:127797019-127797020	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553965865	chr2:127797045-127797046	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs78948193	chr2:127797085-127797086	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs7605172	chr2:127797114-127797115	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555737868	chr2:127797179-127797180	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576029187	chr2:127797185-127797186	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs539959422	chr2:127797258-127797259	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs186355017	chr2:127797291-127797292	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs191271810	chr2:127797309-127797310	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541196423	chr2:127797334-127797335	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs564284698	chr2:127797352-127797353	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181508737	chr2:127797399-127797400	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs552748260	chr2:127797460-127797461	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556657007	chr2:127797494-127797495	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562859761	chr2:127797503-127797504	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559376055	chr2:127797526-127797527	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548577499	chr2:127797542-127797543	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185249179	chr2:127797554-127797555	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116489016	chr2:127797557-127797558	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547543800	chr2:127797569-127797570	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142144954	chr2:127797623-127797624	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539138108	chr2:127797640-127797641	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11902275	chr2:127797656-127797657	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs151222723	chr2:127797711-127797712	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78480303	chr2:127797729-127797730	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555086313	chr2:127797733-127797734	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11898274	chr2:127797741-127797742	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541338588	chr2:127797749-127797750	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139459003	chr2:127797754-127797755	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577949272	chr2:127797759-127797760	Genic enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2795 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127783600-127797000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:127783800-127815600	Weak transcription	Aorta	Aorta
3	chr2:127790400-127797000	Weak transcription	GM12878-XiMat	blood
4	chr2:127793200-127801200	Weak transcription	Fetal Lung	lung
5	chr2:127793200-127805400	Weak transcription	Liver	Liver
6	chr2:127794400-127797000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:127795600-127801400	Weak transcription	Fetal Heart	heart
8	chr2:127795800-127807600	Weak transcription	Brain Germinal Matrix	brain
9	chr2:127796400-127797200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:127797000-127797400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:127797000-127797400	Flanking Active TSS	GM12878-XiMat	blood
12	chr2:127797000-127797600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:127797000-127797600	Enhancers	Primary B cells from peripheral blood	blood
14	chr2:127797000-127797800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr2:127797000-127797800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr2:127797200-127797800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:127797400-127797800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:127797400-127798200	Enhancers	GM12878-XiMat	blood
19	chr2:127797600-127798200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:127797600-127805200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr2:127797800-127798000	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr2:127797800-127803600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:127797800-127805600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr2:127798200-127799200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:127798200-127811400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:127799000-127799800	Enhancers	Brain Cingulate Gyrus	brain
27	chr2:127799200-127799400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:127799200-127799400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:127799200-127799400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr2:127799200-127799800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:127799400-127799600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:127799400-127799600	Enhancers	Brain Angular Gyrus	brain
33	chr2:127799400-127799600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr2:127799400-127799600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:127799400-127799600	Enhancers	Right Ventricle	heart
36	chr2:127799400-127799800	Enhancers	Fetal Kidney	kidney
37	chr2:127799400-127801400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:127799400-127804800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr2:127799600-127801800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:127799600-127803800	Weak transcription	Right Ventricle	heart
41	chr2:127799600-127805800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr2:127799600-127805800	Weak transcription	Gastric	stomach
43	chr2:127799600-127806200	Weak transcription	Brain Angular Gyrus	brain
44	chr2:127799800-127800600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:127799800-127801200	Weak transcription	Fetal Kidney	kidney
46	chr2:127800000-127807600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr2:127800200-127807400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr2:127800400-127800600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:127800400-127802000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:127800600-127801400	Weak transcription	H9 Cell Line	embryonic stem cell

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