Variant report

Variant	esv3394983
Chromosome Location	chr1:241681554-241684102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:490)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:241682922-241683657	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:241683097-241684070	K562	blood:	n/a	n/a
3	ATF1	chr1:241682963-241683569	K562	blood:	n/a	n/a
4	ATF2	chr1:241682785-241683603	GM12878	blood:	n/a	n/a
5	BACH1	chr1:241681762-241682263	K562	blood:	n/a	n/a
6	BACH1	chr1:241682783-241683376	K562	blood:	n/a	n/a
7	BACH1	chr1:241682658-241683183	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr1:241682675-241683423	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:241682415-241683500	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:241681890-241683384	K562	blood:	n/a	n/a
11	BRCA1	chr1:241682758-241684056	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr1:241682907-241683425	K562	blood:	n/a	n/a
13	CBX3	chr1:241682673-241683553	K562	blood:	n/a	n/a
14	CCNT2	chr1:241681980-241683195	K562	blood:	n/a	n/a
15	CEBPB	chr1:241683227-241683447	A549	lung:	n/a	n/a
16	CEBPB	chr1:241682942-241683510	K562	blood:	n/a	n/a
17	CEBPB	chr1:241682849-241683523	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:241682984-241683552	K562	blood:	n/a	n/a
19	CEBPB	chr1:241681818-241682467	Hela-S3	cervix:	n/a	n/a
20	CEBPZ	chr1:241683128-241683344	HepG2	liver:	n/a	n/a
21	CHD1	chr1:241682904-241683031	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr1:241682260-241683621	GM12878	blood:	n/a	n/a
23	CHD2	chr1:241682594-241683368	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:241682065-241683460	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr1:241682837-241683378	GM12878	blood:	n/a	n/a
26	CHD2	chr1:241682770-241683355	HepG2	liver:	n/a	n/a
27	CHD2	chr1:241682603-241683487	K562	blood:	n/a	n/a
28	CREB1	chr1:241682652-241683308	A549	lung:	n/a	n/a
29	CREB1	chr1:241682329-241683509	HepG2	liver:	n/a	n/a
30	CREB1	chr1:241682813-241683393	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr1:241682748-241683438	GM12878	blood:	n/a	n/a
32	CREB1	chr1:241682902-241683165	A549	lung:	n/a	n/a
33	CTBP2	chr1:241682256-241683089	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr1:241682520-241682670	GM12874	blood:	n/a	n/a
35	CTCF	chr1:241682976-241682982	GM12892	blood:	n/a	n/a
36	CTCF	chr1:241682220-241682370	HCM	heart:	n/a	n/a
37	CTCF	chr1:241683111-241683215	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr1:241682443-241682628	GM12878	blood:	n/a	n/a
39	CTCF	chr1:241682220-241682370	NHLF	lung:	n/a	n/a
40	CTCF	chr1:241682312-241682367	GM13977	blood:	n/a	n/a
41	CTCF	chr1:241682540-241682690	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:241682280-241682430	HMEC	breast:	n/a	n/a
43	CTCF	chr1:241682934-241682971	GM12892	blood:	n/a	n/a
44	CTCF	chr1:241683278-241684065	K562	blood:	n/a	n/a
45	CTCF	chr1:241682980-241683130	GM12866	blood:	n/a	n/a
46	CTCF	chr1:241682881-241682974	K562	blood:	n/a	n/a
47	CTCF	chr1:241682200-241682350	SAEC	small airway:	n/a	n/a
48	CTCF	chr1:241682320-241682470	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr1:241682740-241682890	AG04449	skin:	n/a	n/a
50	CTCF	chr1:241683217-241683219	Spleen_OC	spleen:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241682884-241682934	HUVEC	blood vessel:	n/a
2	chr1:241682243-241682293	NH-A	brain:	n/a
3	chr1:241682884-241682934	HUVEC	blood vessel:	n/a
4	chr1:241682243-241682293	NH-A	brain:	n/a
5	chr1:241682243-241682293	MCF-7	breast:	n/a
6	chr1:241682884-241682934	AG04450	lung:	fetal
7	chr1:241682994-241683044	AG10803	skin:	n/a
8	chr1:241683075-241683125	MCF10A-Er-Src	breast:	n/a
9	chr1:241683111-241683161	HUVEC	blood vessel:	n/a
10	chr1:241682884-241682934	SK-N-SH_RA	brain:	n/a
11	chr1:241682243-241682293	PANC-1	pancreas:	n/a
12	chr1:241683161-241683211	SK-N-SH	brain:	n/a
13	chr1:241682627-241682677	ECC-1	luminal epithelium:	n/a
14	chr1:241683161-241683211	IMR90	lung:	fetal
15	chr1:241682243-241682293	NHBE	bronchial:	n/a
16	chr1:241682474-241682524	PANC-1	pancreas:	n/a
17	chr1:241683111-241683161	CMK	blood:	n/a
18	chr1:241682994-241683044	SK-N-SH_RA	brain:	n/a
19	chr1:241682884-241682934	SK-N-MC	brain:	n/a
20	chr1:241682627-241682677	NB4	blood:	n/a
21	chr1:241682884-241682934	MCF10A-Er-Src	breast:	n/a
22	chr1:241683111-241683161	IMR90	lung:	fetal
23	chr1:241682884-241682934	BJ	skin:	n/a
24	chr1:241683111-241683161	SK-N-SH	brain:	n/a
25	chr1:241683111-241683161	NH-A	brain:	n/a
26	chr1:241683075-241683125	HNPCEpiC	eye:	n/a
27	chr1:241683075-241683125	HCT-116	colon:	n/a
28	chr1:241682627-241682677	SK-N-SH	brain:	n/a
29	chr1:241683075-241683125	AoSMC	blood vessel:	n/a
30	chr1:241682627-241682677	K562	blood:	n/a
31	chr1:241682474-241682524	IMR90	lung:	fetal
32	chr1:241682243-241682293	PrEC	prostate:	n/a
33	chr1:241682994-241683044	RPTEC	kidney:	n/a
34	chr1:241682474-241682524	HMEC	breast:	n/a
35	chr1:241682243-241682293	Hepatocyte	liver:	n/a
36	chr1:241683075-241683125	NHBE	bronchial:	n/a
37	chr1:241683075-241683125	GM19239	blood:	n/a
38	chr1:241683161-241683211	CMK	blood:	n/a
39	chr1:241682627-241682677	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:241683161-241683211	ovcar-3	ovarian:	n/a
41	chr1:241682243-241682293	HIPEpiC	eye:	n/a
42	chr1:241682994-241683044	AG09309	skin:	n/a
43	chr1:241682884-241682934	HepG2	liver:	n/a
44	chr1:241683161-241683211	T-47D	breast:	n/a
45	chr1:241682994-241683044	PFSK-1	brain:	n/a
46	chr1:241682474-241682524	PrEC	prostate:	n/a
47	chr1:241682627-241682677	Hepatocyte	liver:	n/a
48	chr1:241682243-241682293	SK-N-SH_RA	brain:	n/a
49	chr1:241682994-241683044	Caco-2	colon:	n/a
50	chr1:241682627-241682677	HCPEpiC	choroid plexus:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:241654504..241656882-chr1:241679445..241682289,2	K562	blood:
2	chr1:241683433..241685881-chr1:241689141..241691385,3	MCF-7	breast:
3	chr1:241680902..241684541-chr1:242009942..242012706,4	K562	blood:
4	chr1:241681898..241684060-chr1:242010602..242013002,4	K562	blood:
5	chr1:241682514..241683274-chr10:38299405..38300057,2	Hela-S3	cervix:
6	chr1:241676840..241679427-chr1:241681305..241683481,5	MCF-7	breast:

No data

Variant related genes	Relation type
FH	TF binding region
FH	CpG island
ENSG00000091483	chromatin interactions
ENSG00000189180	chromatin interactions
ENSG00000174371	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184454255	chr1:241681567-241681568	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs115066813	chr1:241681570-241681571	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562644849	chr1:241681576-241681577	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535226675	chr1:241681621-241681622	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs143616101	chr1:241681653-241681654	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs370118668	chr1:241681668-241681669	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs542068329	chr1:241681672-241681673	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs570348310	chr1:241681750-241681751	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115807771	chr1:241681784-241681785	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs527684225	chr1:241681808-241681809	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs146238498	chr1:241681821-241681822	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs138908865	chr1:241681845-241681846	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs143858517	chr1:241681856-241681857	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs553920974	chr1:241681863-241681864	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs552946925	chr1:241681935-241681936	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs549980685	chr1:241681970-241681971	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs569879316	chr1:241681980-241681981	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535780500	chr1:241681982-241681983	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577238308	chr1:241682071-241682072	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs113467053	chr1:241682077-241682078	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572276528	chr1:241682092-241682093	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555978643	chr1:241682097-241682098	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568008847	chr1:241682127-241682128	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs114561595	chr1:241682136-241682137	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150606543	chr1:241682149-241682150	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs577036247	chr1:241682187-241682188	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs545880709	chr1:241682245-241682246	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556403887	chr1:241682341-241682342	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537370121	chr1:241682355-241682356	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576141558	chr1:241682357-241682358	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375543262	chr1:241682376-241682377	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs541807542	chr1:241682380-241682381	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139786415	chr1:241682408-241682409	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149364921	chr1:241682433-241682434	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541007918	chr1:241682467-241682468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564108869	chr1:241682488-241682489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370323811	chr1:241682532-241682533	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549821066	chr1:241682551-241682552	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs570156656	chr1:241682568-241682569	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs529485494	chr1:241682582-241682583	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs546070504	chr1:241682605-241682606	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs369611362	chr1:241682629-241682630	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs549451094	chr1:241682674-241682675	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs373982143	chr1:241682682-241682683	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs368174074	chr1:241682690-241682691	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs533581397	chr1:241682696-241682697	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs371252889	chr1:241682713-241682714	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs188966702	chr1:241682817-241682818	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs111416913	chr1:241682820-241682821	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112066700	chr1:241682829-241682830	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241659000-241682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:241667400-241681800	Weak transcription	Fetal Brain Male	brain
3	chr1:241667600-241681800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:241667800-241682000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:241668000-241682000	Weak transcription	Pancreas	Pancrea
6	chr1:241668000-241682200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:241668000-241682200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:241668000-241682200	Weak transcription	Esophagus	oesophagus
9	chr1:241671800-241682000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:241672000-241682000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:241672200-241681800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:241673200-241682200	Weak transcription	Spleen	Spleen
13	chr1:241674800-241681800	Weak transcription	Small Intestine	intestine
14	chr1:241674800-241682000	Weak transcription	Colonic Mucosa	Colon
15	chr1:241675400-241681800	Weak transcription	Ovary	ovary
16	chr1:241675600-241681800	Weak transcription	Brain Germinal Matrix	brain
17	chr1:241675800-241681800	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr1:241675800-241681800	Weak transcription	Left Ventricle	heart
19	chr1:241675800-241681800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:241675800-241682000	Weak transcription	Aorta	Aorta
21	chr1:241675800-241682200	Weak transcription	Lung	lung
22	chr1:241676000-241681800	Weak transcription	Psoas Muscle	Psoas
23	chr1:241676000-241682000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:241676000-241682200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr1:241676400-241681800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:241676400-241681800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr1:241676600-241682000	Weak transcription	Placenta	Placenta
28	chr1:241677000-241681800	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr1:241677000-241681800	Weak transcription	HSMM	muscle
30	chr1:241678800-241681600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:241678800-241681600	Weak transcription	Right Atrium	heart
32	chr1:241678800-241682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:241679800-241681800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr1:241680000-241681600	Weak transcription	Fetal Muscle Leg	muscle
35	chr1:241680000-241681800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:241680000-241681800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr1:241680000-241682000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:241680400-241683600	Active TSS	NHLF	lung
39	chr1:241680600-241681600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:241680600-241681600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr1:241680600-241681600	Flanking Active TSS	HUVEC	blood vessel
42	chr1:241680600-241681800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr1:241680600-241681800	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr1:241680600-241681800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:241680600-241681800	Enhancers	Fetal Lung	lung
46	chr1:241680600-241681800	Weak transcription	Fetal Thymus	thymus
47	chr1:241680600-241681800	Enhancers	Rectal Smooth Muscle	rectum
48	chr1:241680600-241681800	Active TSS	K562	blood
49	chr1:241680600-241682000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr1:241680600-241682000	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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