Variant report

Variant	nsv873420
Chromosome Location	chr1:246706139-246755124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1446)
CpG islands
(count:1160)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246740858-246741585	K562	blood:	n/a	chr1:246741392-246741408 chr1:246741393-246741409
2	ARID3A	chr1:246729043-246729235	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:246743156-246743547	K562	blood:	n/a	n/a
4	ARID3A	chr1:246739546-246739738	K562	blood:	n/a	n/a
5	ARID3A	chr1:246750964-246751265	K562	blood:	n/a	n/a
6	ARID3A	chr1:246729459-246729909	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:246745910-246747280	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:246745375-246746415	K562	blood:	n/a	n/a
9	ARID3A	chr1:246740073-246740316	K562	blood:	n/a	n/a
10	ARID3A	chr1:246750866-246751299	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:246730285-246730981	K562	blood:	n/a	n/a
12	ARID3A	chr1:246732646-246733496	K562	blood:	n/a	n/a
13	ARID3A	chr1:246729530-246729980	K562	blood:	n/a	n/a
14	ATF1	chr1:246732872-246733329	K562	blood:	n/a	n/a
15	ATF1	chr1:246740536-246740756	K562	blood:	n/a	n/a
16	ATF1	chr1:246743229-246743481	K562	blood:	n/a	n/a
17	ATF1	chr1:246730636-246730930	K562	blood:	n/a	n/a
18	ATF1	chr1:246740996-246741399	K562	blood:	n/a	n/a
19	ATF2	chr1:246729298-246730096	GM12878	blood:	n/a	n/a
20	ATF2	chr1:246729326-246729950	GM12878	blood:	n/a	n/a
21	ATF2	chr1:246729219-246729717	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr1:246754425-246755257	GM12878	blood:	n/a	n/a
23	ATF2	chr1:246729048-246729793	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr1:246729163-246730103	A549	lung:	n/a	n/a
25	ATF3	chr1:246729333-246729841	A549	lung:	n/a	n/a
26	ATF3	chr1:246734658-246735052	K562	blood:	n/a	n/a
27	BACH1	chr1:246730246-246730860	K562	blood:	n/a	n/a
28	BACH1	chr1:246730812-246730950	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr1:246741033-246741336	K562	blood:	n/a	n/a
30	BACH1	chr1:246732997-246733252	K562	blood:	n/a	n/a
31	BACH1	chr1:246729303-246730285	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr1:246729185-246729841	K562	blood:	n/a	n/a
33	BATF	chr1:246754839-246755255	GM12878	blood:	n/a	n/a
34	BCL3	chr1:246728974-246730135	A549	lung:	n/a	chr1:246729609-246729618
35	BCL3	chr1:246729188-246730094	A549	lung:	n/a	chr1:246729609-246729618
36	BCLAF1	chr1:246740984-246741507	K562	blood:	n/a	n/a
37	BCLAF1	chr1:246729321-246730493	GM12878	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
38	BCLAF1	chr1:246729186-246730406	K562	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
39	BCLAF1	chr1:246754707-246755271	GM12878	blood:	n/a	n/a
40	BCLAF1	chr1:246729322-246730368	GM12878	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
41	BHLHE40	chr1:246739423-246739805	K562	blood:	n/a	chr1:246739593-246739614 chr1:246739599-246739608 chr1:246739597-246739610 chr1:246739599-246739608 chr1:246739600-246739609
42	BHLHE40	chr1:246741097-246741846	K562	blood:	n/a	n/a
43	BHLHE40	chr1:246740142-246740277	K562	blood:	n/a	n/a
44	BHLHE40	chr1:246736925-246737078	A549	lung:	n/a	n/a
45	BHLHE40	chr1:246729205-246730577	GM12878	blood:	n/a	n/a
46	BHLHE40	chr1:246732671-246732792	GM12878	blood:	n/a	n/a
47	BHLHE40	chr1:246734762-246735089	K562	blood:	n/a	n/a
48	BHLHE40	chr1:246732995-246733247	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:246754849-246755249	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:246745708-246746473	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246729578-246729628	SKMC	muscle:	n/a
2	chr1:246729578-246729628	SKMC	muscle:	n/a
3	chr1:246728677-246728727	SK-N-MC	brain:	n/a
4	chr1:246741712-246741762	AG04450	lung:	fetal
5	chr1:246729875-246729925	MCF10A-Er-Src	breast:	n/a
6	chr1:246728677-246728727	HIPEpiC	eye:	n/a
7	chr1:246730188-246730238	AG09319	gingival:	n/a
8	chr1:246729572-246729622	HEEpiC	esophagus:	n/a
9	chr1:246729875-246729925	PrEC	prostate:	n/a
10	chr1:246729218-246729268	PrEC	prostate:	n/a
11	chr1:246729875-246729925	LNCaP	prostate:	n/a
12	chr1:246741712-246741762	Hela-S3	cervix:	n/a
13	chr1:246730219-246730269	NH-A	brain:	n/a
14	chr1:246729345-246729395	GM19239	blood:	n/a
15	chr1:246729345-246729395	BJ	skin:	n/a
16	chr1:246730185-246730235	HRPEpiC	eye:	n/a
17	chr1:246729218-246729268	SAEC	small airway:	n/a
18	chr1:246729345-246729395	HUVEC	blood vessel:	n/a
19	chr1:246729501-246729551	HCT-116	colon:	n/a
20	chr1:246730219-246730269	ovcar-3	ovarian:	n/a
21	chr1:246730188-246730238	HCM	heart:	n/a
22	chr1:246729218-246729268	HCPEpiC	choroid plexus:	n/a
23	chr1:246729578-246729628	GM12892	blood:	n/a
24	chr1:246733057-246733107	MCF10A-Er-Src	breast:	n/a
25	chr1:246733057-246733107	BJ	skin:	n/a
26	chr1:246730188-246730238	ECC-1	luminal epithelium:	n/a
27	chr1:246729669-246729719	HEK293	kidney:	embryo
28	chr1:246741712-246741762	NHBE	bronchial:	n/a
29	chr1:246729585-246729635	PFSK-1	brain:	n/a
30	chr1:246747488-246747538	PFSK-1	brain:	n/a
31	chr1:246747488-246747538	MCF-7	breast:	n/a
32	chr1:246728727-246728777	NH-A	brain:	n/a
33	chr1:246729459-246729509	HCF	heart:	n/a
34	chr1:246730188-246730238	H1-hESC	embryonic stem cell:	embryo
35	chr1:246729572-246729622	HRPEpiC	eye:	n/a
36	chr1:246730219-246730269	PANC-1	pancreas:	n/a
37	chr1:246730219-246730269	ProgFib	skin:	n/a
38	chr1:246729501-246729551	HAEpiC	amniotic membrane:	n/a
39	chr1:246729572-246729622	LNCaP	prostate:	n/a
40	chr1:246741712-246741762	T-47D	breast:	n/a
41	chr1:246729875-246729925	SAEC	small airway:	n/a
42	chr1:246728727-246728777	HCF	heart:	n/a
43	chr1:246730219-246730269	HIPEpiC	eye:	n/a
44	chr1:246730188-246730238	NHBE	bronchial:	n/a
45	chr1:246730185-246730235	Caco-2	colon:	n/a
46	chr1:246733057-246733107	AG09319	gingival:	n/a
47	chr1:246729218-246729268	A549	lung:	n/a
48	chr1:246728727-246728777	Jurkat	blood:	n/a
49	chr1:246729459-246729509	HAEpiC	amniotic membrane:	n/a
50	chr1:246729572-246729622	SKMC	muscle:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246668302..246670787-chr1:246727323..246729930,4	MCF-7	breast:
2	chr1:246729017..246731987-chr1:246738180..246742192,5	MCF-7	breast:
3	chr1:246715254..246717905-chr1:246720739..246723913,4	K562	blood:
4	chr1:246729967..246732161-chr22:19156837..19159425,2	K562	blood:
5	chr1:246745344..246746994-chr1:246750206..246751877,2	MCF-7	breast:
6	chr1:246715254..246717905-chr1:246720739..246723913,4	K562	blood:
7	chr1:246738601..246740180-chr1:246754340..246756772,2	MCF-7	breast:
8	chr1:226185428..226188059-chr1:246740463..246742577,2	K562	blood:
9	chr1:246698102..246699613-chr1:246703690..246706174,2	K562	blood:
10	chr1:246724443..246726246-chr1:246728599..246730567,2	MCF-7	breast:
11	chr1:246729068..246729614-chr3:149530492..149531281,2	Hela-S3	cervix:
12	chr1:246752045..246755966-chr1:246757431..246761107,6	K562	blood:
13	chr1:246730131..246732589-chr1:246747162..246749763,2	MCF-7	breast:
14	chr1:246751383..246754061-chr1:246756080..246758483,2	K562	blood:
15	chr1:246727699..246730587-chr1:246733873..246736383,3	MCF-7	breast:
16	chr1:246729874..246731842-chr1:246862649..246864902,2	K562	blood:
17	chr1:246692831..246695438-chr1:246704915..246707883,3	K562	blood:
18	chr1:246685591..246688881-chr1:246727054..246730014,3	K562	blood:
19	chr1:246711201..246713601-chr1:246713604..246715628,2	K562	blood:
20	chr1:246722538..246724149-chr1:246820776..246822354,2	K562	blood:
21	chr1:246738601..246740180-chr1:246754340..246756772,2	MCF-7	breast:
22	chr1:246752342..246755487-chr1:246758820..246761636,4	K562	blood:
23	chr1:246748858..246751620-chr1:246759232..246762019,2	K562	blood:
24	chr1:246699626..246702195-chr1:246706012..246708369,2	MCF-7	breast:
25	chr1:246739822..246741667-chr1:246766063..246767788,2	K562	blood:
26	chr1:19638692..19639192-chr1:246729163..246730124,2	Hela-S3	cervix:
27	chr1:246668048..246670638-chr1:246738189..246740927,2	K562	blood:
28	chr1:246728909..246731573-chr1:246733348..246738076,5	MCF-7	breast:
29	chr1:246728596..246730970-chr1:246745379..246747536,3	MCF-7	breast:
30	chr1:246745344..246746994-chr1:246750206..246751877,2	MCF-7	breast:
31	chr1:246729197..246730166-chr14:75745608..75746363,2	Hela-S3	cervix:
32	chr1:246749897..246752144-chr1:246758675..246761833,3	K562	blood:
33	chr1:246730131..246732589-chr1:246747162..246749763,2	MCF-7	breast:
34	chr1:246746217..246748591-chr1:246759216..246761418,2	K562	blood:
35	chr1:246711201..246713601-chr1:246713604..246715628,2	K562	blood:
36	chr1:246746503..246747122-chr1:246772184..246772879,2	MCF-7	breast:
37	chr1:246715254..246718890-chr1:246721529..246724491,4	K562	blood:
38	chr1:246715254..246718890-chr1:246721529..246724491,4	K562	blood:
39	chr1:246719266..246723453-chr1:246727295..246731122,5	MCF-7	breast:
40	chr1:246711666..246713604-chr1:246728356..246731058,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMYD3-4	chr1:246714169-246714819	NONHSAT010710
2	lnc-SMYD3-4	chr1:246715093-246715408	NONHSAT010710

No data

Variant related genes	Relation type
CNST	TF binding region
TFB2M	TF binding region
CNST	CpG island
TFB2M	CpG island
ENSG00000242042	chromatin interactions
ENSG00000260924	chromatin interactions
ENSG00000040487	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000227728	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000162852	chromatin interactions

Extended variants
information (count: 2351 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2351 , 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	rs3120701	chr1:246706139-246706140	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543203794	chr1:246706142-246706143	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563190845	chr1:246706144-246706145	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376614984	chr1:246706201-246706202	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77625667	chr1:246706218-246706219	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528936169	chr1:246706234-246706235	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141108322	chr1:246706249-246706250	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3124113	chr1:246706253-246706254	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79846908	chr1:246706286-246706287	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544201196	chr1:246706287-246706288	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11380318	chr1:246706288-246706289	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11420636	chr1:246706309-246706310	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56204224	chr1:246706311-246706312	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558891199	chr1:246706319-246706320	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3124114	chr1:246706347-246706348	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184336257	chr1:246706349-246706350	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571045494	chr1:246706380-246706381	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533725163	chr1:246706386-246706387	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550373074	chr1:246706388-246706389	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189595735	chr1:246706408-246706409	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535918698	chr1:246706434-246706435	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555918231	chr1:246706459-246706460	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78692933	chr1:246706467-246706468	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142695181	chr1:246706492-246706493	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200922554	chr1:246706515-246706516	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141189701	chr1:246706516-246706517	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58742048	chr1:246706519-246706520	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147362600	chr1:246706523-246706524	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150261460	chr1:246706539-246706540	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574849346	chr1:246706595-246706596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535807662	chr1:246706596-246706597	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534718212	chr1:246706598-246706599	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371246902	chr1:246706694-246706695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558174021	chr1:246706708-246706709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182010068	chr1:246706709-246706710	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112769970	chr1:246706710-246706711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185579842	chr1:246706724-246706725	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200503226	chr1:246706728-246706729	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573518516	chr1:246706773-246706774	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542289409	chr1:246706783-246706784	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559190003	chr1:246706793-246706794	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3124115	chr1:246706839-246706840	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs71563788	chr1:246706884-246706885	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544672318	chr1:246706949-246706950	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189530160	chr1:246706983-246706984	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533651827	chr1:246706987-246706988	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550510937	chr1:246707014-246707015	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570233619	chr1:246707020-246707021	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145856305	chr1:246707030-246707031	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3124116	chr1:246707051-246707052	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2520 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246694600-246706600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:246694800-246706600	Weak transcription	Right Ventricle	heart
3	chr1:246699400-246706200	Weak transcription	Spleen	Spleen
4	chr1:246700200-246706400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:246700600-246706400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:246700600-246728200	Weak transcription	Fetal Heart	heart
7	chr1:246700800-246706600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:246701000-246708800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:246701400-246706600	Weak transcription	Psoas Muscle	Psoas
10	chr1:246701400-246708000	Strong transcription	Primary B cells from cord blood	blood
11	chr1:246701600-246706400	Weak transcription	Gastric	stomach
12	chr1:246701600-246710000	Strong transcription	Fetal Muscle Leg	muscle
13	chr1:246701800-246706600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr1:246701800-246713200	Strong transcription	Liver	Liver
15	chr1:246702000-246709000	Strong transcription	Primary T cells from cord blood	blood
16	chr1:246702000-246709800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:246702000-246723800	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr1:246702000-246724400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:246702000-246727200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:246702000-246727200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:246702000-246727600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr1:246702200-246710600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:246702200-246720600	Strong transcription	Duodenum Mucosa	Duodenum
24	chr1:246702200-246720800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr1:246702200-246724600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:246702200-246724600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:246702200-246728200	Weak transcription	Stomach Mucosa	stomach
28	chr1:246702200-246728400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr1:246702400-246721400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr1:246702400-246724400	Strong transcription	Placenta	Placenta
31	chr1:246702400-246726600	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr1:246702600-246706600	Weak transcription	Brain Angular Gyrus	brain
33	chr1:246702600-246713000	Weak transcription	Brain Anterior Caudate	brain
34	chr1:246702800-246706400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:246702800-246709400	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr1:246702800-246726800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr1:246702800-246728600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:246703000-246707600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:246703000-246708000	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr1:246703000-246709400	Strong transcription	Fetal Thymus	thymus
41	chr1:246703000-246710000	Strong transcription	Ovary	ovary
42	chr1:246703000-246727200	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr1:246703200-246714800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:246703200-246724000	Strong transcription	Primary B cells from peripheral blood	blood
45	chr1:246703200-246724200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:246703200-246724400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:246703200-246727400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:246703400-246706400	Weak transcription	Pancreas	Pancrea
49	chr1:246703600-246706400	Strong transcription	NH-A	brain
50	chr1:246703600-246708200	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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