Variant report

Variant	nsv583739
Chromosome Location	chr2:178942302-178993562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178974597-178974930	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:178974581-178974935	K562	blood:	n/a	n/a
3	ARID3A	chr2:178976898-178977429	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:178976920-178977251	K562	blood:	n/a	n/a
5	ATF2	chr2:178976877-178977311	GM12878	blood:	n/a	n/a
6	ATF2	chr2:178976818-178977303	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:178976920-178977397	GM12878	blood:	n/a	n/a
8	ATF2	chr2:178976825-178977263	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr2:178976882-178977268	K562	blood:	n/a	n/a
10	ATF3	chr2:178976839-178977460	A549	lung:	n/a	n/a
11	BACH1	chr2:178976842-178977310	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:178976994-178977120	K562	blood:	n/a	n/a
13	BCL3	chr2:178976764-178977570	A549	lung:	n/a	chr2:178977137-178977145
14	BCL3	chr2:178976708-178977347	A549	lung:	n/a	chr2:178977137-178977145
15	BCLAF1	chr2:178976940-178977327	K562	blood:	n/a	chr2:178977137-178977145
16	BCLAF1	chr2:178976884-178977609	GM12878	blood:	n/a	chr2:178977137-178977145
17	BCLAF1	chr2:178976838-178977436	GM12878	blood:	n/a	chr2:178977137-178977145
18	BHLHE40	chr2:178976931-178977398	K562	blood:	n/a	chr2:178977085-178977101
19	BHLHE40	chr2:178976965-178977652	GM12878	blood:	n/a	chr2:178977085-178977101
20	BRCA1	chr2:178976874-178977278	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr2:178976932-178977574	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:178976977-178977271	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:178976944-178977264	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr2:178976858-178977273	K562	blood:	n/a	n/a
25	CBX3	chr2:178976748-178977833	HCT-116	colon:	n/a	n/a
26	CBX3	chr2:178960221-178960596	K562	blood:	n/a	n/a
27	CBX3	chr2:178976819-178977515	K562	blood:	n/a	n/a
28	CBX3	chr2:178976684-178977547	HCT-116	colon:	n/a	n/a
29	CBX3	chr2:178966009-178966407	K562	blood:	n/a	n/a
30	CCNT2	chr2:178976937-178977633	K562	blood:	n/a	n/a
31	CEBPB	chr2:178974143-178974273	K562	blood:	n/a	chr2:178974181-178974192
32	CEBPB	chr2:178976727-178977277	A549	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
33	CEBPB	chr2:178976793-178977445	GM12878	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
34	CEBPB	chr2:178976623-178977534	HCT-116	colon:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
35	CEBPB	chr2:178976675-178977379	K562	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
36	CEBPB	chr2:178978943-178978969	A549	lung:	n/a	n/a
37	CEBPB	chr2:178976791-178977201	K562	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
38	CEBPB	chr2:178949020-178949330	H1-hESC	embryonic stem cell:	n/a	chr2:178949132-178949141 chr2:178949130-178949143 chr2:178949132-178949143 chr2:178949132-178949141 chr2:178949132-178949141 chr2:178949130-178949141 chr2:178949132-178949141
39	CEBPB	chr2:178976600-178977396	A549	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
40	CEBPB	chr2:178976794-178977258	H1-hESC	embryonic stem cell:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
41	CEBPB	chr2:178976793-178977216	IMR90	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
42	CEBPB	chr2:178976832-178977171	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
43	CEBPB	chr2:178974078-178974316	IMR90	lung:	n/a	chr2:178974181-178974192
44	CEBPB	chr2:178948977-178949357	A549	lung:	n/a	chr2:178949132-178949141 chr2:178949130-178949143 chr2:178949132-178949143 chr2:178949132-178949141 chr2:178949132-178949141 chr2:178949130-178949141 chr2:178949132-178949141
45	CEBPB	chr2:178949096-178949421	MCF-7	breast:	n/a	chr2:178949132-178949141 chr2:178949130-178949143 chr2:178949132-178949143 chr2:178949132-178949141 chr2:178949132-178949141 chr2:178949130-178949141 chr2:178949132-178949141
46	CEBPB	chr2:178976809-178977343	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
47	CEBPB	chr2:178976675-178977347	MCF-7	breast:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
48	CEBPB	chr2:178976811-178977243	K562	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
49	CEBPB	chr2:178976565-178977402	MCF-7	breast:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
50	CEBPB	chr2:178948969-178949346	HepG2	liver:	n/a	chr2:178949132-178949141 chr2:178949130-178949143 chr2:178949132-178949143 chr2:178949132-178949141 chr2:178949132-178949141 chr2:178949130-178949141 chr2:178949132-178949141

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178977979-178978029	ProgFib	skin:	n/a
2	chr2:178977818-178977868	GM12892	blood:	n/a
3	chr2:178977979-178978029	ProgFib	skin:	n/a
4	chr2:178977818-178977868	GM12892	blood:	n/a
5	chr2:178975712-178975762	CMK	blood:	n/a
6	chr2:178973065-178973115	BE2_C	brain:	n/a
7	chr2:178973216-178973266	SK-N-SH_RA	brain:	n/a
8	chr2:178977979-178978029	MCF10A-Er-Src	breast:	n/a
9	chr2:178973147-178973197	HAEpiC	amniotic membrane:	n/a
10	chr2:178977979-178978029	HCM	heart:	n/a
11	chr2:178973251-178973301	U87	brain:	n/a
12	chr2:178977079-178977129	HUVEC	blood vessel:	n/a
13	chr2:178973216-178973266	HEK293	kidney:	embryo
14	chr2:178973065-178973115	HCT-116	colon:	n/a
15	chr2:178973019-178973069	ProgFib	skin:	n/a
16	chr2:178973092-178973142	HCF	heart:	n/a
17	chr2:178977002-178977052	H1-hESC	embryonic stem cell:	embryo
18	chr2:178975712-178975762	BE2_C	brain:	n/a
19	chr2:178976295-178976345	NHDF-neo	bronchial:	n/a
20	chr2:178976981-178977031	GM12892	blood:	n/a
21	chr2:178974175-178974225	BE2_C	brain:	n/a
22	chr2:178973065-178973115	AG09319	gingival:	n/a
23	chr2:178973019-178973069	PANC-1	pancreas:	n/a
24	chr2:178973147-178973197	AoSMC	blood vessel:	n/a
25	chr2:178976295-178976345	HCF	heart:	n/a
26	chr2:178976254-178976304	BE2_C	brain:	n/a
27	chr2:178970574-178970624	BE2_C	brain:	n/a
28	chr2:178973065-178973115	HRE	kidney:	n/a
29	chr2:178976254-178976304	AG10803	skin:	n/a
30	chr2:178973079-178973129	HCM	heart:	n/a
31	chr2:178976981-178977031	AG09309	skin:	n/a
32	chr2:178970574-178970624	AG04449	skin:	fetal
33	chr2:178974175-178974225	PrEC	prostate:	n/a
34	chr2:178977081-178977131	GM12891	blood:	n/a
35	chr2:178976361-178976411	HCM	heart:	n/a
36	chr2:178974175-178974225	HNPCEpiC	eye:	n/a
37	chr2:178975712-178975762	HMEC	breast:	n/a
38	chr2:178981007-178981057	NH-A	brain:	n/a
39	chr2:178977002-178977052	NHBE	bronchial:	n/a
40	chr2:178976254-178976304	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:178976981-178977031	PrEC	prostate:	n/a
42	chr2:178973147-178973197	HEK293	kidney:	embryo
43	chr2:178977818-178977868	MCF10A-Er-Src	breast:	n/a
44	chr2:178973164-178973214	HAEpiC	amniotic membrane:	n/a
45	chr2:178976254-178976304	HL-60	blood:	n/a
46	chr2:178973019-178973069	HEK293	kidney:	embryo
47	chr2:178977002-178977052	PFSK-1	brain:	n/a
48	chr2:178973092-178973142	Hela-S3	cervix:	n/a
49	chr2:178976361-178976411	NB4	blood:	n/a
50	chr2:178970574-178970624	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:178940677..178943272-chr2:178945277..178948244,4	K562	blood:
2	chr2:178939852..178942987-chr2:178976321..178978354,3	K562	blood:
3	chr2:178975761..178978600-chr2:179056476..179059620,3	K562	blood:
4	chr2:178959487..178962376-chr2:178976482..178978600,2	MCF-7	breast:
5	chr2:178974519..178975080-chr2:179279294..179279980,2	MCF-7	breast:
6	chr2:178981148..178983862-chr2:179057589..179059906,2	MCF-7	breast:
7	chr2:178993079..178995697-chr2:179002423..179004658,2	K562	blood:
8	chr2:178977795..178981676-chr2:178993113..178997821,5	K562	blood:
9	chr2:178980858..178983485-chr2:178983971..178985850,2	K562	blood:
10	chr2:178974271..178975212-chr2:179283614..179284146,3	MCF-7	breast:
11	chr2:178991568..178995332-chr2:178996165..178998325,3	MCF-7	breast:
12	chr2:178978462..178980467-chr2:179057158..179058664,2	MCF-7	breast:
13	chr2:178978517..178980297-chr2:179707105..179709962,2	K562	blood:
14	chr2:178757808..178759787-chr2:178940377..178942583,2	K562	blood:
15	chr2:178977351..178979746-chr2:178983845..178986068,3	K562	blood:
16	chr2:178951510..178953164-chr2:178957903..178959538,2	K562	blood:
17	chr2:178982755..178985967-chr2:178987271..178990939,3	K562	blood:
18	chr2:178976973..178979935-chr2:178988410..178990810,2	K562	blood:
19	chr2:178981363..178983943-chr2:179315477..179318383,2	K562	blood:
20	chr2:178951510..178953164-chr2:178957903..178959538,2	K562	blood:
21	chr2:178977125..178980608-chr2:178981010..178983814,6	K562	blood:
22	chr2:178987630..178989492-chr2:178991140..178993708,2	K562	blood:
23	chr2:178972756..178975132-chr2:178975866..178978416,2	MCF-7	breast:
24	chr2:178940297..178942724-chr2:178946031..178947901,2	K562	blood:
25	chr2:178940999..178943053-chr2:178957174..178959156,2	K562	blood:
26	chr2:178970656..178974678-chr2:178975520..178979270,3	K562	blood:
27	chr2:178975067..178978289-chr2:179058254..179060575,4	MCF-7	breast:
28	chr2:178976973..178979935-chr2:178988410..178990810,2	K562	blood:
29	chr2:178847948..178848513-chr2:178974436..178975057,2	MCF-7	breast:
30	chr2:178955531..178957949-chr2:178963225..178965293,2	K562	blood:
31	chr2:178936273..178939016-chr2:178945956..178948361,3	K562	blood:
32	chr2:178940677..178943272-chr2:178945277..178948244,4	K562	blood:
33	chr2:178970656..178974678-chr2:178975520..178979270,3	K562	blood:
34	chr2:178986068..178988538-chr2:178997888..179000584,2	K562	blood:
35	chr2:178991876..178994492-chr2:179011398..179013023,2	K562	blood:
36	chr2:178975231..178977429-chr2:179315218..179317152,2	MCF-7	breast:
37	chr2:178972756..178975132-chr2:178975866..178978416,2	MCF-7	breast:
38	chr2:178952298..178954111-chr2:178975625..178977992,2	K562	blood:
39	chr2:178974511..178975026-chr2:179283583..179284286,2	K562	blood:
40	chr2:178985399..178987987-chr2:179314612..179317404,2	MCF-7	breast:
41	chr2:178973629..178974622-chr2:179240854..179241453,2	MCF-7	breast:
42	chr2:178974133..178981122-chr2:179276785..179281060,9	K562	blood:
43	chr2:178940999..178943053-chr2:178957174..178959156,2	K562	blood:
44	chr2:178965236..178967731-chr2:178970870..178972647,2	K562	blood:
45	chr2:178974721..178975261-chr2:179285955..179286795,2	K562	blood:
46	chr2:178977222..178979193-chr2:179277270..179279929,2	MCF-7	breast:
47	chr2:178935372..178939354-chr2:178942023..178945915,4	K562	blood:
48	chr2:178979115..178980922-chr2:179059390..179062250,2	K562	blood:
49	chr2:178960724..178963095-chr2:178966189..178968403,2	MCF-7	breast:
50	chr2:178976808..178978488-chr2:179342162..179344754,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSBPL6-3	chr2:178990866-178990911	NONHSAT075737
2	lnc-RBM45-1	chr2:178986636-178987086	ucscGeneNc_uc002umb_1

Variant related genes	Relation type
CYCTP	TF binding region
PDE11A	TF binding region
RBM45	TF binding region
ENSG00000227241	TF binding region
CYCTP	CpG island
PDE11A	CpG island
RBM45	CpG island
ENSG00000227241	CpG island
ENSG00000079156	chromatin interactions
ENSG00000128655	chromatin interactions
ENSG00000180228	chromatin interactions
ENSG00000079150	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000155636	chromatin interactions
ENSG00000223960	chromatin interactions

Extended variants
information (count: 1362 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6710329	chr2:178942302-178942303	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576081286	chr2:178942309-178942310	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571877372	chr2:178942312-178942313	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184908445	chr2:178942323-178942324	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561933856	chr2:178942380-178942381	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs13032997	chr2:178942395-178942396	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs13033229	chr2:178942471-178942472	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs13033237	chr2:178942519-178942520	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112571520	chr2:178942528-178942529	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13033250	chr2:178942529-178942530	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs77385086	chr2:178942652-178942653	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374509923	chr2:178942655-178942656	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143799511	chr2:178942688-178942689	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369684271	chr2:178942736-178942737	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540850628	chr2:178942746-178942747	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs1435572	chr2:178942789-178942790	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs368668659	chr2:178942804-178942805	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs532034375	chr2:178942847-178942848	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs4436997	chr2:178942884-178942885	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552106984	chr2:178942923-178942924	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568985696	chr2:178942926-178942927	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs80155484	chr2:178942973-178942974	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs13397185	chr2:178942977-178942978	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568241136	chr2:178942998-178942999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534130093	chr2:178943011-178943012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187469853	chr2:178943012-178943013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192800044	chr2:178943041-178943042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13397357	chr2:178943097-178943098	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79630526	chr2:178943169-178943170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543110395	chr2:178943182-178943183	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200939294	chr2:178943197-178943198	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200794869	chr2:178943198-178943199	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs5836642	chr2:178943199-178943200	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201771495	chr2:178943200-178943201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200087103	chr2:178943202-178943203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141325181	chr2:178943233-178943234	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561687039	chr2:178943271-178943272	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145077379	chr2:178943314-178943315	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541916247	chr2:178943338-178943339	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555566054	chr2:178943387-178943388	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572323463	chr2:178943461-178943462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550086962	chr2:178943472-178943473	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184907746	chr2:178943485-178943486	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528857468	chr2:178943526-178943527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533638537	chr2:178943530-178943531	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs13397839	chr2:178943567-178943568	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561222751	chr2:178943580-178943581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138864949	chr2:178943647-178943648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532161058	chr2:178943729-178943730	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548291785	chr2:178943735-178943736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
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
Seminomas	18059402	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	21720365	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	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	chr2:178946200-178946400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr2:178946200-178946600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr2:178946200-178946600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr2:178946200-178946800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr2:178946200-178946800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:178946800-178947200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:178947200-178947400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr2:178947200-178947600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:178947200-178947800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:178952400-178954600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr2:178952600-178952800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr2:178952600-178954800	Enhancers	Fetal Intestine Large	intestine
13	chr2:178953000-178954800	Enhancers	Fetal Intestine Small	intestine
14	chr2:178953800-178954200	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr2:178954000-178954200	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr2:178965800-178966400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:178966000-178966600	Enhancers	K562	blood
18	chr2:178966000-178966600	Enhancers	NHDF-Ad	bronchial
19	chr2:178966600-178970400	Weak transcription	K562	blood
20	chr2:178967800-178968800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:178970400-178970600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:178970400-178970600	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr2:178970400-178971200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:178971200-178976800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:178973000-178973200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:178973200-178977000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:178974800-178975000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr2:178975000-178976400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr2:178975600-178976600	Enhancers	NHEK	skin
30	chr2:178976200-178976400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr2:178976400-178976600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:178976400-178976600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:178976400-178976600	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr2:178976400-178976600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr2:178976400-178976600	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr2:178976400-178976600	Enhancers	Dnd41	blood
37	chr2:178976400-178976800	Enhancers	Primary T cells from cord blood	blood
38	chr2:178976400-178976800	Enhancers	Primary T cells fromperipheralblood	blood
39	chr2:178976400-178976800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr2:178976400-178976800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr2:178976400-178976800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr2:178976400-178976800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr2:178976400-178976800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:178976400-178976800	Enhancers	Placenta	Placenta
45	chr2:178976400-178976800	Enhancers	Hela-S3	cervix
46	chr2:178976400-178976800	Enhancers	HMEC	breast
47	chr2:178976400-178977000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr2:178976600-178976800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr2:178976600-178976800	Enhancers	Primary B cells from peripheral blood	blood
50	chr2:178976600-178976800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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