Variant report

Variant	nsv522036
Chromosome Location	chr2:179395760-179398509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:734)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:179395108-179396236	GM12878	blood:	n/a	n/a
2	ATF2	chr2:179394891-179396186	GM12878	blood:	n/a	n/a
3	BATF	chr2:179395174-179395863	GM12878	blood:	n/a	n/a
4	BATF	chr2:179395261-179395830	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:179395225-179395856	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:179395162-179395911	GM12878	blood:	n/a	n/a
7	BCL3	chr2:179395365-179395837	GM12878	blood:	n/a	n/a
8	BCL3	chr2:179395262-179395880	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:179395119-179396036	GM12878	blood:	n/a	n/a
10	BCLAF1	chr2:179395028-179396123	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:179395075-179396058	GM12878	blood:	n/a	n/a
12	CEBPB	chr2:179395072-179396538	GM12878	blood:	n/a	n/a
13	CHD2	chr2:179395248-179395910	GM12878	blood:	n/a	n/a
14	CREB1	chr2:179395167-179396390	GM12878	blood:	n/a	n/a
15	CREB1	chr2:179394878-179396695	GM12878	blood:	n/a	n/a
16	CTCF	chr2:179395533-179395902	GM12878	blood:	n/a	n/a
17	CUX1	chr2:179394953-179396053	GM12878	blood:	n/a	n/a
18	EBF1	chr2:179395108-179396076	GM12878	blood:	n/a	chr2:179395626-179395637
19	EBF1	chr2:179395028-179396165	GM12878	blood:	n/a	chr2:179395626-179395637
20	EBF1	chr2:179395174-179396034	GM12878	blood:	n/a	chr2:179395626-179395637
21	ELF1	chr2:179395273-179395862	GM12878	blood:	n/a	n/a
22	EP300	chr2:179395047-179395929	GM12878	blood:	n/a	n/a
23	EP300	chr2:179394963-179396406	GM12878	blood:	n/a	n/a
24	FOXM1	chr2:179395113-179396083	GM12878	blood:	n/a	n/a
25	FOXM1	chr2:179394964-179395977	GM12878	blood:	n/a	n/a
26	IKZF1	chr2:179394867-179395784	GM12878	blood:	n/a	n/a
27	IRF4	chr2:179395147-179395964	GM12878	blood:	n/a	n/a
28	IRF4	chr2:179395070-179395943	GM12878	blood:	n/a	n/a
29	MAX	chr2:179395249-179395987	GM12878	blood:	n/a	n/a
30	MAX	chr2:179394947-179395925	NB4	blood:	n/a	n/a
31	MAZ	chr2:179395273-179396165	GM12878	blood:	n/a	n/a
32	MEF2A	chr2:179395208-179395851	GM12878	blood:	n/a	n/a
33	MEF2A	chr2:179395198-179395825	GM12878	blood:	n/a	n/a
34	MTA3	chr2:179394980-179396344	GM12878	blood:	n/a	n/a
35	MTA3	chr2:179395084-179396490	GM12878	blood:	n/a	n/a
36	MXI1	chr2:179395285-179396002	GM12878	blood:	n/a	n/a
37	MYC	chr2:179394847-179396014	NB4	blood:	n/a	n/a
38	NFATC1	chr2:179395199-179395951	GM12878	blood:	n/a	n/a
39	NFATC1	chr2:179395071-179396152	GM12878	blood:	n/a	n/a
40	NFIC	chr2:179394857-179395905	GM12878	blood:	n/a	n/a
41	NFIC	chr2:179394482-179396690	GM12878	blood:	n/a	n/a
42	PAX5	chr2:179395093-179396241	GM12878	blood:	n/a	n/a
43	PAX5	chr2:179395323-179396175	GM12878	blood:	n/a	n/a
44	PAX5	chr2:179395393-179396063	GM12891	blood:	n/a	n/a
45	PAX5	chr2:179395280-179396124	GM12878	blood:	n/a	n/a
46	PAX5	chr2:179395754-179396024	GM12878	blood:	n/a	n/a
47	PML	chr2:179394857-179396205	GM12878	blood:	n/a	n/a
48	PML	chr2:179395208-179395782	GM12878	blood:	n/a	n/a
49	POLR2A	chr2:179395585-179395915	GM12878	blood:	n/a	n/a
50	POLR2A	chr2:179395160-179396133	GM12878	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179397435-179397485	AG09309	skin:	n/a
2	chr2:179396826-179396876	HNPCEpiC	eye:	n/a
3	chr2:179397435-179397485	AG09309	skin:	n/a
4	chr2:179396826-179396876	HNPCEpiC	eye:	n/a
5	chr2:179396688-179396738	H1-hESC	embryonic stem cell:	embryo
6	chr2:179396214-179396264	HMEC	breast:	n/a
7	chr2:179395935-179395985	ECC-1	luminal epithelium:	n/a
8	chr2:179396214-179396264	SK-N-SH_RA	brain:	n/a
9	chr2:179397008-179397058	Hela-S3	cervix:	n/a
10	chr2:179396750-179396800	Hela-S3	cervix:	n/a
11	chr2:179395885-179395935	HCT-116	colon:	n/a
12	chr2:179397435-179397485	AoSMC	blood vessel:	n/a
13	chr2:179397483-179397533	SK-N-MC	brain:	n/a
14	chr2:179397483-179397533	GM12892	blood:	n/a
15	chr2:179395912-179395962	H1-hESC	embryonic stem cell:	embryo
16	chr2:179397483-179397533	HCPEpiC	choroid plexus:	n/a
17	chr2:179396688-179396738	GM12892	blood:	n/a
18	chr2:179396688-179396738	NB4	blood:	n/a
19	chr2:179397435-179397485	GM19239	blood:	n/a
20	chr2:179396826-179396876	A549	lung:	n/a
21	chr2:179395912-179395962	HNPCEpiC	eye:	n/a
22	chr2:179395885-179395935	HCF	heart:	n/a
23	chr2:179396214-179396264	SK-N-MC	brain:	n/a
24	chr2:179397008-179397058	GM12878	blood:	n/a
25	chr2:179397435-179397485	GM06990	blood:	n/a
26	chr2:179395885-179395935	NH-A	brain:	n/a
27	chr2:179396750-179396800	Caco-2	colon:	n/a
28	chr2:179397483-179397533	HCT-116	colon:	n/a
29	chr2:179397483-179397533	SK-N-SH	brain:	n/a
30	chr2:179397435-179397485	NHDF-neo	bronchial:	n/a
31	chr2:179396214-179396264	HRPEpiC	eye:	n/a
32	chr2:179397435-179397485	HRCEpiC	kidney:	n/a
33	chr2:179397008-179397058	SK-N-SH_RA	brain:	n/a
34	chr2:179397435-179397485	HUVEC	blood vessel:	n/a
35	chr2:179397435-179397485	MCF-7	breast:	n/a
36	chr2:179395935-179395985	AG04450	lung:	fetal
37	chr2:179396688-179396738	T-47D	breast:	n/a
38	chr2:179395885-179395935	HCPEpiC	choroid plexus:	n/a
39	chr2:179397008-179397058	HL-60	blood:	n/a
40	chr2:179396214-179396264	MCF-7	breast:	n/a
41	chr2:179396688-179396738	IMR90	lung:	fetal
42	chr2:179395912-179395962	HRPEpiC	eye:	n/a
43	chr2:179396214-179396264	HNPCEpiC	eye:	n/a
44	chr2:179396750-179396800	GM12892	blood:	n/a
45	chr2:179397435-179397485	GM12892	blood:	n/a
46	chr2:179396750-179396800	ECC-1	luminal epithelium:	n/a
47	chr2:179396688-179396738	U87	brain:	n/a
48	chr2:179396688-179396738	AG04450	lung:	fetal
49	chr2:179396214-179396264	GM19239	blood:	n/a
50	chr2:179397008-179397058	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:179395770..179398427-chr2:179417927..179420746,2	K562	blood:
2	chr2:179386919..179391089-chr2:179391647..179398872,11	K562	blood:
3	chr2:179386627..179389310-chr2:179394176..179396606,2	MCF-7	breast:
4	chr2:179395497..179400266-chr2:179412543..179417721,4	K562	blood:
5	chr2:179343546..179345499-chr2:179398217..179400353,2	K562	blood:
6	chr2:179336273..179338307-chr2:179397796..179400668,2	K562	blood:

No data

Variant related genes	Relation type
TTN-AS1	TF binding region
TTN-AS1	CpG island
ENSG00000116095	chromatin interactions
ENSG00000237298	chromatin interactions
ENSG00000270277	chromatin interactions

Extended variants
information (count: 191 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:191 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3829749	chr2:179395760-179395761	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377340289	chr2:179395772-179395773	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199469665	chr2:179395811-179395812	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs55865284	chr2:179395813-179395814	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573843615	chr2:179395826-179395827	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532236466	chr2:179395829-179395830	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs200123047	chr2:179395852-179395853	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372263729	chr2:179395860-179395861	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs55806007	chr2:179395874-179395875	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs538363206	chr2:179395875-179395876	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs554953169	chr2:179395893-179395894	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568472002	chr2:179395912-179395913	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368591364	chr2:179395913-179395914	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534484592	chr2:179395919-179395920	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371893623	chr2:179395924-179395925	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200782068	chr2:179395926-179395927	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368992068	chr2:179395930-179395931	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554213990	chr2:179395935-179395936	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs372875128	chr2:179395936-179395937	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs3813250	chr2:179395958-179395959	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs369608299	chr2:179395970-179395971	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546048021	chr2:179396006-179396007	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373073929	chr2:179396031-179396032	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs556741970	chr2:179396081-179396082	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs397517795	chr2:179396082-179396083	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs55938627	chr2:179396114-179396115	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs3813249	chr2:179396130-179396131	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs2857269	chr2:179396149-179396150	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371075036	chr2:179396159-179396160	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs56308529	chr2:179396162-179396163	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376175862	chr2:179396193-179396194	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540500017	chr2:179396206-179396207	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370137295	chr2:179396214-179396215	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200378865	chr2:179396215-179396216	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552058608	chr2:179396251-179396252	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs72629789	chr2:179396252-179396253	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374678473	chr2:179396257-179396258	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs56001826	chr2:179396259-179396260	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368779151	chr2:179396293-179396294	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568460311	chr2:179396305-179396306	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533966614	chr2:179396311-179396312	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116876353	chr2:179396329-179396330	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs397517794	chr2:179396349-179396350	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs3829748	chr2:179396354-179396355	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs397517793	chr2:179396357-179396358	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368945564	chr2:179396364-179396365	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372312805	chr2:179396399-179396400	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376634193	chr2:179396406-179396407	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs267599019	chr2:179396413-179396414	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs267599020	chr2:179396425-179396426	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179388800-179395800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:179388800-179395800	Weak transcription	Placenta	Placenta
3	chr2:179388800-179395800	Weak transcription	Lung	lung
4	chr2:179388800-179396000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:179388800-179396200	Weak transcription	Fetal Kidney	kidney
6	chr2:179388800-179396200	Weak transcription	Gastric	stomach
7	chr2:179388800-179396200	Weak transcription	Pancreas	Pancrea
8	chr2:179388800-179403600	Weak transcription	Esophagus	oesophagus
9	chr2:179388800-179408000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:179388800-179408600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr2:179388800-179410600	Weak transcription	Colonic Mucosa	Colon
12	chr2:179388800-179411800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:179388800-179417600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:179388800-179429400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:179388800-179441800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr2:179388800-179448800	Weak transcription	Small Intestine	intestine
17	chr2:179388800-179495800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr2:179389000-179395800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:179389000-179395800	Weak transcription	Aorta	Aorta
20	chr2:179389000-179396000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr2:179389000-179396000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:179389000-179396000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr2:179389000-179396200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:179389000-179396200	Weak transcription	Brain Substantia Nigra	brain
25	chr2:179389000-179396200	Weak transcription	Fetal Brain Female	brain
26	chr2:179389200-179396200	Weak transcription	Brain Anterior Caudate	brain
27	chr2:179389200-179396200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr2:179389200-179412600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:179389400-179395800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr2:179389400-179396000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr2:179389400-179396000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:179389400-179396000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:179389400-179396000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:179389400-179396000	Weak transcription	Brain Angular Gyrus	brain
35	chr2:179389400-179396000	Weak transcription	Fetal Lung	lung
36	chr2:179389400-179396000	Weak transcription	Ovary	ovary
37	chr2:179389400-179396000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr2:179389400-179396000	Weak transcription	A549	lung
39	chr2:179389400-179396200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:179389400-179396200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:179389400-179396200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:179389400-179396200	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr2:179389400-179396200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:179389400-179396200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:179389400-179396200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:179389400-179396200	Weak transcription	Liver	Liver
47	chr2:179389400-179396200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr2:179389400-179396200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr2:179389400-179396200	Weak transcription	Colon Smooth Muscle	Colon
50	chr2:179389400-179396200	Weak transcription	Duodenum Mucosa	Duodenum

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