Variant report

Variant	esv1806558
Chromosome Location	chr1:228358977-228365154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:135)
CpG islands
(count:427)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:135 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:228362247-228362422	K562	blood:	n/a	n/a
2	CBX3	chr1:228362119-228362489	K562	blood:	n/a	n/a
3	CCNT2	chr1:228361622-228362663	K562	blood:	n/a	n/a
4	CCNT2	chr1:228363472-228363655	K562	blood:	n/a	n/a
5	CREB1	chr1:228362102-228362403	A549	lung:	n/a	n/a
6	CREB1	chr1:228361626-228361893	A549	lung:	n/a	n/a
7	CTCF	chr1:228362140-228362290	GM12869	blood:	n/a	chr1:228362249-228362262
8	CTCF	chr1:228362192-228362353	H1-hESC	embryonic stem cell:	n/a	chr1:228362249-228362262
9	CTCF	chr1:228362135-228362426	K562	blood:	n/a	chr1:228362249-228362262
10	CTCF	chr1:228362220-228362370	K562	blood:	n/a	chr1:228362249-228362262
11	CTCF	chr1:228360880-228361030	NHEK	skin:	n/a	n/a
12	CTCF	chr1:228362200-228362350	NHEK	skin:	n/a	chr1:228362249-228362262
13	CTCF	chr1:228361706-228361745	NHEK	skin:	n/a	n/a
14	CTCF	chr1:228360840-228360990	HepG2	liver:	n/a	n/a
15	CTCF	chr1:228362360-228362510	AG04449	skin:	n/a	n/a
16	CTCF	chr1:228362180-228362330	HCT-116	colon:	n/a	chr1:228362249-228362262
17	CTCF	chr1:228362260-228362410	HRE	kidney:	n/a	n/a
18	CTCF	chr1:228362220-228362370	HEK293	kidney:	n/a	chr1:228362249-228362262
19	CTCFL	chr1:228362163-228362352	K562	blood:	n/a	n/a
20	E2F6	chr1:228362357-228362521	K562	blood:	n/a	n/a
21	EBF1	chr1:228363973-228364133	GM12878	blood:	n/a	n/a
22	EGR1	chr1:228362133-228362317	K562	blood:	n/a	n/a
23	EGR1	chr1:228362424-228362666	K562	blood:	n/a	n/a
24	EGR1	chr1:228362360-228362627	K562	blood:	n/a	n/a
25	ELF1	chr1:228361609-228361892	K562	blood:	n/a	n/a
26	ETS1	chr1:228362171-228362359	K562	blood:	n/a	n/a
27	FOXA1	chr1:228362142-228362358	T-47D	breast:	n/a	n/a
28	FOXA1	chr1:228361463-228361825	T-47D	breast:	n/a	n/a
29	GABPA	chr1:228362297-228362673	K562	blood:	n/a	n/a
30	GABPA	chr1:228362163-228362792	K562	blood:	n/a	n/a
31	GTF2F1	chr1:228361611-228361772	K562	blood:	n/a	n/a
32	HCFC1	chr1:228362156-228362568	K562	blood:	n/a	n/a
33	HEY1	chr1:228362180-228362479	K562	blood:	n/a	n/a
34	HMGN3	chr1:228361404-228362692	K562	blood:	n/a	n/a
35	HMGN3	chr1:228362970-228363170	K562	blood:	n/a	n/a
36	IRF1	chr1:228361595-228362487	K562	blood:	n/a	n/a
37	JUND	chr1:228362202-228362417	K562	blood:	n/a	n/a
38	MAFK	chr1:228362351-228362470	K562	blood:	n/a	n/a
39	MAX	chr1:228362080-228362391	K562	blood:	n/a	chr1:228362364-228362373 chr1:228362371-228362381
40	MAX	chr1:228361707-228361848	K562	blood:	n/a	n/a
41	MAX	chr1:228362143-228362378	K562	blood:	n/a	chr1:228362364-228362373
42	MAX	chr1:228362125-228362642	K562	blood:	n/a	chr1:228362364-228362373 chr1:228362371-228362381
43	MAX	chr1:228362121-228362635	ECC-1	luminal epithelium:	n/a	chr1:228362364-228362373 chr1:228362371-228362381
44	MAX	chr1:228361502-228361881	ECC-1	luminal epithelium:	n/a	n/a
45	MAX	chr1:228361238-228361892	MCF-7	breast:	n/a	n/a
46	MAX	chr1:228361587-228361877	K562	blood:	n/a	n/a
47	MAX	chr1:228359817-228360271	K562	blood:	n/a	n/a
48	MAX	chr1:228361667-228361827	K562	blood:	n/a	n/a
49	MAZ	chr1:228361788-228361827	K562	blood:	n/a	n/a
50	MAZ	chr1:228362115-228362522	K562	blood:	n/a	chr1:228362364-228362373 chr1:228362371-228362381

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228362309-228362359	SAEC	small airway:	n/a
2	chr1:228362509-228362559	HEK293	kidney:	embryo
3	chr1:228362309-228362359	HL-60	blood:	n/a
4	chr1:228359130-228359180	GM12891	blood:	n/a
5	chr1:228361641-228361691	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:228360531-228360581	T-47D	breast:	n/a
7	chr1:228363521-228363571	GM12892	blood:	n/a
8	chr1:228361641-228361691	CMK	blood:	n/a
9	chr1:228362443-228362493	AG10803	skin:	n/a
10	chr1:228361641-228361691	PrEC	prostate:	n/a
11	chr1:228360531-228360581	ovcar-3	ovarian:	n/a
12	chr1:228363521-228363571	PFSK-1	brain:	n/a
13	chr1:228363521-228363571	NHBE	bronchial:	n/a
14	chr1:228362309-228362359	HAEpiC	amniotic membrane:	n/a
15	chr1:228360531-228360581	CMK	blood:	n/a
16	chr1:228363521-228363571	HepG2	liver:	n/a
17	chr1:228362309-228362359	SK-N-MC	brain:	n/a
18	chr1:228362309-228362359	ECC-1	luminal epithelium:	n/a
19	chr1:228362509-228362559	NHBE	bronchial:	n/a
20	chr1:228360531-228360581	HEEpiC	esophagus:	n/a
21	chr1:228362309-228362359	BE2_C	brain:	n/a
22	chr1:228360531-228360581	HEK293	kidney:	embryo
23	chr1:228362443-228362493	Jurkat	blood:	n/a
24	chr1:228362443-228362493	HUVEC	blood vessel:	n/a
25	chr1:228362509-228362559	Caco-2	colon:	n/a
26	chr1:228360531-228360581	Caco-2	colon:	n/a
27	chr1:228360531-228360581	GM12878	blood:	n/a
28	chr1:228362509-228362559	NHDF-neo	bronchial:	n/a
29	chr1:228362509-228362559	H1-hESC	embryonic stem cell:	embryo
30	chr1:228361641-228361691	LNCaP	prostate:	n/a
31	chr1:228359130-228359180	NHBE	bronchial:	n/a
32	chr1:228362309-228362359	HCF	heart:	n/a
33	chr1:228361641-228361691	HCF	heart:	n/a
34	chr1:228360531-228360581	ProgFib	skin:	n/a
35	chr1:228362509-228362559	A549	lung:	n/a
36	chr1:228359130-228359180	HCPEpiC	choroid plexus:	n/a
37	chr1:228361641-228361691	PFSK-1	brain:	n/a
38	chr1:228362309-228362359	RPTEC	kidney:	n/a
39	chr1:228360531-228360581	HCF	heart:	n/a
40	chr1:228362509-228362559	GM12891	blood:	n/a
41	chr1:228362509-228362559	GM19239	blood:	n/a
42	chr1:228363521-228363571	GM19239	blood:	n/a
43	chr1:228362309-228362359	HUVEC	blood vessel:	n/a
44	chr1:228362509-228362559	HCPEpiC	choroid plexus:	n/a
45	chr1:228362443-228362493	HRE	kidney:	n/a
46	chr1:228360531-228360581	SK-N-MC	brain:	n/a
47	chr1:228361641-228361691	HIPEpiC	eye:	n/a
48	chr1:228359130-228359180	H1-hESC	embryonic stem cell:	embryo
49	chr1:228362509-228362559	HRCEpiC	kidney:	n/a
50	chr1:228361641-228361691	SK-N-MC	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228356236..228360236-chr1:228642827..228646319,4	K562	blood:
2	chr1:228296474..228298184-chr1:228362327..228363984,2	K562	blood:
3	chr1:228350414..228357594-chr1:228359448..228365919,31	MCF-7	breast:
4	chr1:228352925..228354845-chr1:228364134..228367346,3	MCF-7	breast:
5	chr1:228359729..228361744-chr1:228520707..228523201,2	K562	blood:
6	chr1:228350980..228355955-chr1:228356979..228359321,5	MCF-7	breast:
7	chr1:228359558..228361063-chr1:228363819..228365618,2	MCF-7	breast:
8	chr1:228359558..228361063-chr1:228363819..228365618,2	MCF-7	breast:
9	chr1:228362968..228364679-chr1:228382995..228385252,2	K562	blood:
10	chr1:228360767..228363057-chr1:228399837..228402220,2	MCF-7	breast:
11	chr1:228301175..228302855-chr1:228364193..228366742,2	K562	blood:
12	chr1:228296791..228299072-chr1:228362296..228364108,2	MCF-7	breast:
13	chr1:228295591..228297111-chr1:228358549..228360057,2	K562	blood:
14	chr1:228320957..228324264-chr1:228357884..228361663,3	MCF-7	breast:
15	chr1:228362275..228366557-chr1:228367502..228371326,4	MCF-7	breast:
16	chr1:228295318..228298683-chr1:228360322..228363984,4	K562	blood:
17	chr1:228362964..228365740-chr1:228389422..228392205,2	K562	blood:
18	chr1:228362342..228364297-chr1:228644461..228646357,2	K562	blood:
19	chr1:228269154..228271874-chr1:228360119..228363775,3	K562	blood:
20	chr1:228361423..228364297-chr1:228644461..228646940,2	K562	blood:
21	chr1:228331165..228333412-chr1:228361433..228363518,2	MCF-7	breast:
22	chr1:228357413..228360288-chr1:228642904..228645646,2	K562	blood:

No data

Variant related genes	Relation type
IBA57	TF binding region
IBA57	CpG island
ENSG00000181218	chromatin interactions
ENSG00000196890	chromatin interactions
ENSG00000154358	chromatin interactions
ENSG00000227625	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000162913	chromatin interactions
ENSG00000143761	chromatin interactions
ENSG00000162910	chromatin interactions
ENSG00000143774	chromatin interactions
ENSG00000181873	chromatin interactions

Extended variants
information (count: 289 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574976790	chr1:228358993-228358994	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs543715224	chr1:228359019-228359020	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs41314262	chr1:228359075-228359076	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs192127004	chr1:228359078-228359079	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs184217966	chr1:228359131-228359132	Weak transcription Strong transcription	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs371959331	chr1:228359149-228359150	Weak transcription Strong transcription	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs144250988	chr1:228359296-228359297	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs3795771	chr1:228359355-228359356	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs147765981	chr1:228359360-228359361	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs547491586	chr1:228359370-228359371	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs560872590	chr1:228359410-228359411	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs560569352	chr1:228359412-228359413	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs375235610	chr1:228359445-228359446	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs529910109	chr1:228359462-228359463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs1934882	chr1:228359463-228359464	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569592084	chr1:228359521-228359522	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs1934881	chr1:228359541-228359542	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552118508	chr1:228359583-228359584	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs189375973	chr1:228359595-228359596	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs3795773	chr1:228359630-228359631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs577707524	chr1:228359642-228359643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs546562335	chr1:228359651-228359652	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs559781920	chr1:228359699-228359700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs537646953	chr1:228359734-228359735	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs557618049	chr1:228359736-228359737	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs71710690	chr1:228359770-228359771	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs78598870	chr1:228359771-228359772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs2066237	chr1:228359775-228359776	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs200101937	chr1:228359778-228359779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs78255226	chr1:228359779-228359780	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs202018862	chr1:228359780-228359781	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs72757808	chr1:228359782-228359783	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs373595910	chr1:228359785-228359786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs146349457	chr1:228359791-228359792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs563247143	chr1:228359797-228359798	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs59008692	chr1:228359846-228359847	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs80262175	chr1:228359847-228359848	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs201683283	chr1:228359857-228359858	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs141476466	chr1:228359863-228359864	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs564849143	chr1:228359870-228359871	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs78642527	chr1:228359871-228359872	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs540729625	chr1:228359872-228359873	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs548466411	chr1:228359881-228359882	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs561030692	chr1:228359882-228359883	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs572447405	chr1:228359896-228359897	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs529779075	chr1:228359898-228359899	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs562229412	chr1:228359920-228359921	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs563158260	chr1:228359936-228359937	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs375580590	chr1:228359963-228359964	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs74142621	chr1:228359972-228359973	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	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
Prostate cancer	18632612	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
Endometrioid adenocarcinoma	16974079	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
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228354400-228362600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:228354400-228384600	Weak transcription	Aorta	Aorta
3	chr1:228354600-228359400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:228354600-228360400	Weak transcription	Gastric	stomach
5	chr1:228354600-228361200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:228354600-228362200	Weak transcription	Brain Germinal Matrix	brain
7	chr1:228354600-228362200	Weak transcription	Fetal Thymus	thymus
8	chr1:228354600-228362400	Weak transcription	Psoas Muscle	Psoas
9	chr1:228354600-228363600	Weak transcription	Primary B cells from cord blood	blood
10	chr1:228354600-228370400	Weak transcription	Right Atrium	heart
11	chr1:228354600-228382200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:228354600-228385200	Weak transcription	Left Ventricle	heart
13	chr1:228354800-228359000	Weak transcription	Fetal Kidney	kidney
14	chr1:228354800-228360000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr1:228354800-228360200	Weak transcription	Right Ventricle	heart
16	chr1:228354800-228360400	Weak transcription	Pancreas	Pancrea
17	chr1:228354800-228360400	Weak transcription	Spleen	Spleen
18	chr1:228354800-228360800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:228354800-228361000	Weak transcription	Fetal Brain Female	brain
20	chr1:228354800-228361200	Weak transcription	Fetal Lung	lung
21	chr1:228354800-228361400	Weak transcription	Esophagus	oesophagus
22	chr1:228354800-228361400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:228354800-228361400	Weak transcription	A549	lung
24	chr1:228354800-228361600	Weak transcription	Colonic Mucosa	Colon
25	chr1:228354800-228362200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:228354800-228362200	Weak transcription	NHLF	lung
27	chr1:228354800-228362400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr1:228354800-228362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:228354800-228362400	Weak transcription	Adipose Nuclei	Adipose
30	chr1:228354800-228362400	Weak transcription	Brain Anterior Caudate	brain
31	chr1:228354800-228362400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:228354800-228362400	Weak transcription	Fetal Brain Male	brain
33	chr1:228354800-228362600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr1:228354800-228362600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:228354800-228362600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:228354800-228362600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr1:228354800-228362800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr1:228354800-228362800	Weak transcription	Brain Angular Gyrus	brain
39	chr1:228354800-228362800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr1:228354800-228362800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr1:228354800-228363400	Weak transcription	Colon Smooth Muscle	Colon
42	chr1:228354800-228364400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:228354800-228364400	Weak transcription	Brain Substantia Nigra	brain
44	chr1:228354800-228364600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:228354800-228365200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:228354800-228366400	Weak transcription	Liver	Liver
47	chr1:228354800-228367000	Weak transcription	Osteobl	bone
48	chr1:228354800-228370800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr1:228354800-228371200	Weak transcription	HSMMtube	muscle
50	chr1:228354800-228373200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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