Variant report

Variant	nsv539002
Chromosome Location	chr7:86691235-86770796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:642)
CpG islands
(count:61)
Chromatin interactive
region (count:107)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:86740005-86740535	K562	blood:	n/a	n/a
2	ARID3A	chr7:86737302-86737337	K562	blood:	n/a	n/a
3	ARID3A	chr7:86731548-86732062	K562	blood:	n/a	n/a
4	ARID3A	chr7:86769622-86770338	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:86768794-86770104	K562	blood:	n/a	n/a
6	ARID3A	chr7:86724644-86724647	K562	blood:	n/a	n/a
7	ARID3A	chr7:86705733-86705820	K562	blood:	n/a	n/a
8	ARID3A	chr7:86735687-86736939	K562	blood:	n/a	n/a
9	ARID3A	chr7:86750518-86750622	K562	blood:	n/a	n/a
10	ARID3A	chr7:86733627-86733731	K562	blood:	n/a	n/a
11	ARID3A	chr7:86740797-86740810	K562	blood:	n/a	n/a
12	ARID3A	chr7:86737613-86738710	K562	blood:	n/a	n/a
13	ARID3A	chr7:86752167-86752697	K562	blood:	n/a	n/a
14	ATF1	chr7:86748214-86748282	K562	blood:	n/a	n/a
15	ATF1	chr7:86729978-86730226	K562	blood:	n/a	n/a
16	ATF1	chr7:86736557-86736891	K562	blood:	n/a	n/a
17	ATF1	chr7:86716824-86716865	K562	blood:	n/a	n/a
18	ATF1	chr7:86739719-86740489	K562	blood:	n/a	n/a
19	ATF1	chr7:86769526-86770113	K562	blood:	n/a	n/a
20	ATF1	chr7:86758303-86758764	K562	blood:	n/a	n/a
21	ATF1	chr7:86704306-86704315	K562	blood:	n/a	n/a
22	ATF2	chr7:86756201-86757113	GM12878	blood:	n/a	n/a
23	ATF2	chr7:86758961-86759719	GM12878	blood:	n/a	n/a
24	ATF2	chr7:86759035-86759598	GM12878	blood:	n/a	n/a
25	ATF3	chr7:86740059-86740448	K562	blood:	n/a	n/a
26	ATF3	chr7:86769572-86770110	K562	blood:	n/a	n/a
27	BACH1	chr7:86768985-86769203	K562	blood:	n/a	n/a
28	BACH1	chr7:86722018-86722117	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr7:86737972-86737973	K562	blood:	n/a	n/a
30	BACH1	chr7:86722837-86722969	K562	blood:	n/a	n/a
31	BACH1	chr7:86740684-86740686	K562	blood:	n/a	n/a
32	BATF	chr7:86759154-86759547	GM12878	blood:	n/a	n/a
33	BATF	chr7:86756367-86756624	GM12878	blood:	n/a	n/a
34	BATF	chr7:86759151-86759532	GM12878	blood:	n/a	n/a
35	BATF	chr7:86756304-86756719	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:86759152-86759575	GM12878	blood:	n/a	n/a
37	BCL3	chr7:86759152-86759535	GM12878	blood:	n/a	n/a
38	BCLAF1	chr7:86758978-86759575	GM12878	blood:	n/a	chr7:86759135-86759144
39	BHLHE40	chr7:86741230-86741573	K562	blood:	n/a	n/a
40	BHLHE40	chr7:86751691-86751693	K562	blood:	n/a	n/a
41	BHLHE40	chr7:86736379-86736848	K562	blood:	n/a	n/a
42	BHLHE40	chr7:86752639-86752658	K562	blood:	n/a	n/a
43	BHLHE40	chr7:86768871-86769036	K562	blood:	n/a	n/a
44	BHLHE40	chr7:86769625-86770250	K562	blood:	n/a	n/a
45	BHLHE40	chr7:86737353-86738057	K562	blood:	n/a	n/a
46	BHLHE40	chr7:86738291-86738459	K562	blood:	n/a	n/a
47	BHLHE40	chr7:86740034-86740631	K562	blood:	n/a	n/a
48	BRCA1	chr7:86770097-86770297	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:86769552-86769812	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr7:86697070-86697441	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:86758571-86758621	HCF	heart:	n/a
2	chr7:86758571-86758621	Jurkat	blood:	n/a
3	chr7:86758571-86758621	HEK293	kidney:	embryo
4	chr7:86758571-86758621	Hela-S3	cervix:	n/a
5	chr7:86758571-86758621	ECC-1	luminal epithelium:	n/a
6	chr7:86758571-86758621	LNCaP	prostate:	n/a
7	chr7:86758571-86758621	K562	blood:	n/a
8	chr7:86758571-86758621	SAEC	small airway:	n/a
9	chr7:86758571-86758621	BJ	skin:	n/a
10	chr7:86758571-86758621	A549	lung:	n/a
11	chr7:86758571-86758621	HUVEC	blood vessel:	n/a
12	chr7:86758571-86758621	NB4	blood:	n/a
13	chr7:86758571-86758621	PrEC	prostate:	n/a
14	chr7:86758571-86758621	GM19239	blood:	n/a
15	chr7:86758571-86758621	HEEpiC	esophagus:	n/a
16	chr7:86758571-86758621	PFSK-1	brain:	n/a
17	chr7:86758571-86758621	GM12892	blood:	n/a
18	chr7:86758571-86758621	HCM	heart:	n/a
19	chr7:86758571-86758621	Hepatocyte	liver:	n/a
20	chr7:86758571-86758621	HCT-116	colon:	n/a
21	chr7:86758571-86758621	SKMC	muscle:	n/a
22	chr7:86758571-86758621	HRCEpiC	kidney:	n/a
23	chr7:86758571-86758621	SK-N-SH_RA	brain:	n/a
24	chr7:86758571-86758621	CMK	blood:	n/a
25	chr7:86758571-86758621	RPTEC	kidney:	n/a
26	chr7:86758571-86758621	HRE	kidney:	n/a
27	chr7:86758571-86758621	MCF10A-Er-Src	breast:	n/a
28	chr7:86758571-86758621	U87	brain:	n/a
29	chr7:86758571-86758621	HRPEpiC	eye:	n/a
30	chr7:86758571-86758621	HL-60	blood:	n/a
31	chr7:86758571-86758621	HMEC	breast:	n/a
32	chr7:86758571-86758621	GM06990	blood:	n/a
33	chr7:86758571-86758621	MCF-7	breast:	n/a
34	chr7:86758571-86758621	AG09309	skin:	n/a
35	chr7:86758571-86758621	H1-hESC	embryonic stem cell:	embryo
36	chr7:86758571-86758621	NHDF-neo	bronchial:	n/a
37	chr7:86758571-86758621	NT2-D1	testis:	n/a
38	chr7:86758571-86758621	ovcar-3	ovarian:	n/a
39	chr7:86758571-86758621	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:86758571-86758621	SK-N-SH	brain:	n/a
41	chr7:86758571-86758621	NH-A	brain:	n/a
42	chr7:86758571-86758621	HNPCEpiC	eye:	n/a
43	chr7:86758571-86758621	BE2_C	brain:	n/a
44	chr7:86758571-86758621	IMR90	lung:	fetal
45	chr7:86758571-86758621	HAEpiC	amniotic membrane:	n/a
46	chr7:86758571-86758621	Caco-2	colon:	n/a
47	chr7:86758571-86758621	GM12891	blood:	n/a
48	chr7:86758571-86758621	T-47D	breast:	n/a
49	chr7:86758571-86758621	HCPEpiC	choroid plexus:	n/a
50	chr7:86758571-86758621	AG09319	gingival:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:86717691..86719505-chr7:86725972..86728347,2	K562	blood:
2	chr7:86687904..86689831-chr7:86767827..86771326,5	K562	blood:
3	chr7:86689181..86691875-chr7:86696290..86698415,2	K562	blood:
4	chr7:86758520..86760252-chr7:86782060..86784571,2	K562	blood:
5	chr7:86685184..86687724-chr7:86697845..86699925,2	K562	blood:
6	chr7:86747236..86750092-chr7:86777747..86780252,2	K562	blood:
7	chr7:86743993..86746929-chr7:86777540..86779629,2	K562	blood:
8	chr7:86704472..86706406-chr7:86758436..86761205,2	K562	blood:
9	chr7:86715699..86717658-chr7:86720284..86723135,2	K562	blood:
10	chr7:86678036..86679789-chr7:86754886..86757474,2	K562	blood:
11	chr7:86730349..86731920-chr7:86762742..86764645,2	K562	blood:
12	chr7:86718315..86719969-chr7:86722285..86724739,2	MCF-7	breast:
13	chr7:86715699..86717658-chr7:86720284..86723135,2	K562	blood:
14	chr7:86701831..86703604-chr7:86708934..86710753,2	K562	blood:
15	chr7:86753870..86756288-chr7:86781219..86783671,3	K562	blood:
16	chr7:86730153..86732657-chr7:86734174..86736967,2	K562	blood:
17	chr7:86757205..86760252-chr7:86779952..86783560,4	K562	blood:
18	chr7:86717691..86719505-chr7:86725972..86728347,2	K562	blood:
19	chr7:86726160..86728980-chr7:86729415..86731972,2	K562	blood:
20	chr7:86732466..86733997-chr7:86781558..86783748,2	K562	blood:
21	chr7:86686224..86689375-chr7:86696561..86699925,3	K562	blood:
22	chr7:86710313..86711993-chr7:86721437..86723544,2	K562	blood:
23	chr7:86701144..86703992-chr7:86710903..86713321,2	K562	blood:
24	chr7:86760460..86762904-chr7:86763165..86765693,2	MCF-7	breast:
25	chr7:86689181..86691875-chr7:86696290..86698415,2	K562	blood:
26	chr7:86736144..86740329-chr7:86781903..86788552,7	K562	blood:
27	chr7:86763222..86765945-chr7:86765955..86768293,2	K562	blood:
28	chr7:86743955..86746564-chr7:86769711..86772412,2	K562	blood:
29	chr7:86687259..86690064-chr7:86758649..86761060,2	MCF-7	breast:
30	chr7:86719703..86722390-chr7:86737277..86739102,2	K562	blood:
31	chr7:86744672..86746680-chr7:86750084..86752305,2	K562	blood:
32	chr7:86688083..86692094-chr7:86768272..86771491,3	K562	blood:
33	chr7:86729004..86730749-chr7:86793705..86795432,2	K562	blood:
34	chr7:86653737..86655666-chr7:86769659..86772034,2	K562	blood:
35	chr7:86748494..86751720-chr7:86753396..86757160,5	K562	blood:
36	chr7:86708698..86710998-chr7:86712777..86716552,3	K562	blood:
37	chr7:86689009..86690709-chr7:86703392..86706204,2	MCF-7	breast:
38	chr7:86721191..86723956-chr7:86776438..86778233,2	MCF-7	breast:
39	chr7:86687878..86690022-chr7:86750207..86751897,2	MCF-7	breast:
40	chr7:86726970..86728474-chr7:86738214..86739716,2	K562	blood:
41	chr7:86751698..86753266-chr7:86780497..86782723,2	K562	blood:
42	chr7:86735133..86740177-chr7:86744513..86748479,5	K562	blood:
43	chr7:86684095..86686938-chr7:86700649..86703002,2	K562	blood:
44	chr17:55048854..55051126-chr7:86715574..86718478,2	MCF-7	breast:
45	chr7:86711462..86714724-chr7:86716535..86719053,3	K562	blood:
46	chr7:86718315..86719969-chr7:86722285..86724739,2	MCF-7	breast:
47	chr7:86710213..86713085-chr7:86780614..86783888,3	K562	blood:
48	chr7:86700000..86704458-chr7:86705805..86710434,5	K562	blood:
49	chr7:86746755..86750570-chr7:86763189..86766191,3	K562	blood:
50	chr7:86686668..86692984-chr7:86780038..86786500,15	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMTF1-2	chr7:86750544-86750721	NONHSAT121808
2	lnc-DMTF1-2	chr7:86747721-86747906	NONHSAT121808
3	lnc-DMTF1-1	chr7:86738855-86740598	ENSG00000261462.1

No data

Variant related genes	Relation type
ENSG00000261462	TF binding region
KIAA1324L	TF binding region
ENSG00000261462	CpG island
KIAA1324L	CpG island
ENSG00000261462	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000224046	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000164659	chromatin interactions

Extended variants
information (count: 2396 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79999859	chr7:86691237-86691238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529928943	chr7:86691251-86691252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs13243613	chr7:86691254-86691255	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs369779692	chr7:86691273-86691274	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs569866666	chr7:86691286-86691287	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs193018262	chr7:86691351-86691352	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs114048711	chr7:86691386-86691387	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555478676	chr7:86691389-86691390	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573250601	chr7:86691411-86691412	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184868420	chr7:86691443-86691444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs146676589	chr7:86691446-86691447	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188415965	chr7:86691456-86691457	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529631331	chr7:86691457-86691458	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577183686	chr7:86691523-86691524	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs73200970	chr7:86691526-86691527	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs201307245	chr7:86691571-86691572	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs191389100	chr7:86691662-86691663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183608658	chr7:86691685-86691686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530420544	chr7:86691712-86691713	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542808951	chr7:86691761-86691762	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs13234254	chr7:86691792-86691793	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528559931	chr7:86691987-86691988	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10282112	chr7:86692019-86692020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571577302	chr7:86692063-86692064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372965895	chr7:86692069-86692070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs377163688	chr7:86692131-86692132	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369747440	chr7:86692138-86692139	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372999370	chr7:86692187-86692188	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs376459898	chr7:86692202-86692203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370938698	chr7:86692217-86692218	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373357845	chr7:86692272-86692273	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200620470	chr7:86692409-86692410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539982259	chr7:86692552-86692553	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs532504803	chr7:86692568-86692569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs551712116	chr7:86692602-86692603	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs376280500	chr7:86692739-86692740	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201243589	chr7:86692753-86692754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs569958187	chr7:86692780-86692781	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs202000908	chr7:86692807-86692808	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537290922	chr7:86692861-86692862	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374120528	chr7:86692898-86692899	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs367857083	chr7:86692907-86692908	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs548884073	chr7:86692937-86692938	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs567389475	chr7:86692939-86692940	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs199857046	chr7:86692940-86692941	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs534434669	chr7:86692959-86692960	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs369378925	chr7:86692987-86692988	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs552985804	chr7:86693030-86693031	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs201973432	chr7:86693045-86693046	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs577227613	chr7:86693047-86693048	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86690200-86697200	Weak transcription	K562	blood
2	chr7:86697200-86698000	Enhancers	K562	blood
3	chr7:86698000-86698400	Weak transcription	K562	blood
4	chr7:86700400-86700600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:86700600-86701200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:86701000-86702400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:86701200-86701400	Enhancers	K562	blood
8	chr7:86701200-86702200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:86702200-86703800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:86703800-86704400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:86703800-86705400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:86705000-86705200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
13	chr7:86705000-86705400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:86705000-86705400	Bivalent Enhancer	Primary B cells from cord blood	blood
15	chr7:86705000-86705600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:86705000-86705800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr7:86705000-86705800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:86705000-86706200	Enhancers	Primary T cells from cord blood	blood
19	chr7:86705200-86705600	Enhancers	GM12878-XiMat	blood
20	chr7:86705200-86705800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:86705200-86705800	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr7:86705400-86705800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr7:86705600-86705800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr7:86713000-86714800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:86713400-86714200	Enhancers	K562	blood
26	chr7:86713400-86714200	Enhancers	NHDF-Ad	bronchial
27	chr7:86713800-86715400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:86720800-86721200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:86720800-86721600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr7:86721000-86721600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr7:86721200-86721600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:86724400-86725200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr7:86724400-86725200	Enhancers	NHDF-Ad	bronchial
34	chr7:86729000-86730600	Enhancers	NHEK	skin
35	chr7:86729200-86729400	Enhancers	HSMMtube	muscle
36	chr7:86729200-86730400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:86729200-86730400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:86729200-86730600	Enhancers	HMEC	breast
39	chr7:86729400-86730600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:86729600-86730400	Enhancers	Hela-S3	cervix
41	chr7:86730200-86730400	Enhancers	K562	blood
42	chr7:86731000-86732200	Weak transcription	K562	blood
43	chr7:86732200-86733800	Enhancers	K562	blood
44	chr7:86732600-86734000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:86732800-86733600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:86733200-86733600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:86733200-86734000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:86733600-86740800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:86735000-86736000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:86735200-86736800	Enhancers	NHDF-Ad	bronchial

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