Variant report

Variant	nsv1005824
Chromosome Location	chr1:225114654-225158871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:550)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225117357-225117517	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225121406-225121573	K562	blood:	n/a	n/a
3	ARID3A	chr1:225133723-225134019	HepG2	liver:	n/a	n/a
4	ATF1	chr1:225117958-225118374	K562	blood:	n/a	n/a
5	ATF1	chr1:225117186-225117593	K562	blood:	n/a	n/a
6	BACH1	chr1:225117256-225117761	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr1:225117146-225117805	K562	blood:	n/a	chr1:225117736-225117749 chr1:225117633-225117642 chr1:225117589-225117602
8	BCLAF1	chr1:225117128-225117697	K562	blood:	n/a	chr1:225117633-225117642 chr1:225117589-225117602
9	BHLHE40	chr1:225117300-225117534	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:225117111-225117835	K562	blood:	n/a	chr1:225117729-225117745 chr1:225117726-225117742 chr1:225117661-225117677
11	BRCA1	chr1:225117057-225117517	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:225117895-225118265	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr1:225117860-225118566	K562	blood:	n/a	n/a
14	CBX3	chr1:225120283-225120696	K562	blood:	n/a	n/a
15	CBX3	chr1:225116851-225117850	K562	blood:	n/a	n/a
16	CBX3	chr1:225117244-225117645	K562	blood:	n/a	n/a
17	CBX3	chr1:225119590-225120029	K562	blood:	n/a	n/a
18	CBX3	chr1:225121024-225122475	K562	blood:	n/a	n/a
19	CBX3	chr1:225120286-225120710	K562	blood:	n/a	n/a
20	CBX3	chr1:225121107-225121821	K562	blood:	n/a	n/a
21	CBX3	chr1:225116923-225117782	HCT-116	colon:	n/a	n/a
22	CCNT2	chr1:225117187-225117853	K562	blood:	n/a	n/a
23	CEBPB	chr1:225144265-225144303	A549	lung:	n/a	n/a
24	CEBPB	chr1:225133801-225133998	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:225116949-225117427	K562	blood:	n/a	n/a
26	CEBPB	chr1:225133750-225134015	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:225117173-225117383	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:225133722-225134046	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:225117078-225117548	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:225133720-225134060	HepG2	liver:	n/a	n/a
31	CEBPD	chr1:225117147-225117762	K562	blood:	n/a	n/a
32	CEBPD	chr1:225133749-225134036	HepG2	liver:	n/a	n/a
33	CEBPD	chr1:225117177-225117620	HepG2	liver:	n/a	n/a
34	CHD2	chr1:225117087-225117806	K562	blood:	n/a	n/a
35	CHD2	chr1:225133782-225133865	HepG2	liver:	n/a	n/a
36	CHD2	chr1:225117252-225117503	GM12878	blood:	n/a	n/a
37	CHD2	chr1:225117009-225117563	HepG2	liver:	n/a	n/a
38	CHD2	chr1:225117067-225117792	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:225117048-225117800	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr1:225117117-225118412	K562	blood:	n/a	n/a
41	CREB1	chr1:225117131-225117688	A549	lung:	n/a	n/a
42	CREB1	chr1:225117014-225117862	HepG2	liver:	n/a	n/a
43	CREB1	chr1:225117919-225118399	K562	blood:	n/a	n/a
44	CREB1	chr1:225117996-225118305	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr1:225117287-225117592	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr1:225133800-225133950	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr1:225117376-225117579	Fibrobl	skin:	n/a	n/a
48	CTCF	chr1:225117580-225117730	HepG2	liver:	n/a	n/a
49	CTCF	chr1:225133719-225134021	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:225133705-225133909	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225117817-225117867	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:225117817-225117867	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:225117431-225117481	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:225150341-225150391	MCF10A-Er-Src	breast:	n/a
5	chr1:225117464-225117514	CMK	blood:	n/a
6	chr1:225117464-225117514	A549	lung:	n/a
7	chr1:225117676-225117726	HRCEpiC	kidney:	n/a
8	chr1:225117750-225117800	ovcar-3	ovarian:	n/a
9	chr1:225117817-225117867	HMEC	breast:	n/a
10	chr1:225116995-225117045	Hepatocyte	liver:	n/a
11	chr1:225117676-225117726	HUVEC	blood vessel:	n/a
12	chr1:225117464-225117514	NH-A	brain:	n/a
13	chr1:225117389-225117439	HEK293	kidney:	embryo
14	chr1:225117676-225117726	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:225117389-225117439	AG04450	lung:	fetal
16	chr1:225117676-225117726	AG10803	skin:	n/a
17	chr1:225117431-225117481	NH-A	brain:	n/a
18	chr1:225117676-225117726	GM12891	blood:	n/a
19	chr1:225117076-225117126	HepG2	liver:	n/a
20	chr1:225116995-225117045	GM12892	blood:	n/a
21	chr1:225150341-225150391	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:225117750-225117800	HRE	kidney:	n/a
23	chr1:225116995-225117045	IMR90	lung:	fetal
24	chr1:225117389-225117439	IMR90	lung:	fetal
25	chr1:225117750-225117800	A549	lung:	n/a
26	chr1:225117389-225117439	AG04449	skin:	fetal
27	chr1:225150341-225150391	PrEC	prostate:	n/a
28	chr1:225117464-225117514	AG10803	skin:	n/a
29	chr1:225150341-225150391	GM19239	blood:	n/a
30	chr1:225117431-225117481	LNCaP	prostate:	n/a
31	chr1:225150341-225150391	HepG2	liver:	n/a
32	chr1:225117464-225117514	HRPEpiC	eye:	n/a
33	chr1:225117389-225117439	ProgFib	skin:	n/a
34	chr1:225117464-225117514	GM12892	blood:	n/a
35	chr1:225117464-225117514	Jurkat	blood:	n/a
36	chr1:225117817-225117867	GM06990	blood:	n/a
37	chr1:225117389-225117439	Hela-S3	cervix:	n/a
38	chr1:225117464-225117514	AG04449	skin:	fetal
39	chr1:225117464-225117514	AG04450	lung:	fetal
40	chr1:225117431-225117481	Hela-S3	cervix:	n/a
41	chr1:225117750-225117800	HCPEpiC	choroid plexus:	n/a
42	chr1:225117464-225117514	SAEC	small airway:	n/a
43	chr1:225117817-225117867	HRCEpiC	kidney:	n/a
44	chr1:225150341-225150391	SKMC	muscle:	n/a
45	chr1:225117817-225117867	AG04450	lung:	fetal
46	chr1:225117817-225117867	SKMC	muscle:	n/a
47	chr1:225117431-225117481	HRPEpiC	eye:	n/a
48	chr1:225117389-225117439	HRE	kidney:	n/a
49	chr1:225116995-225117045	NHDF-neo	bronchial:	n/a
50	chr1:225117750-225117800	GM12891	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:225117903..225119549-chr1:225136065..225137999,2	K562	blood:
2	chr1:225116699..225117668-chr3:73160108..73161088,2	Hela-S3	cervix:
3	chr1:225125254..225128428-chr1:225150698..225154229,3	K562	blood:
4	chr1:225133403..225135871-chr1:225146349..225149223,2	K562	blood:
5	chr1:225117293..225117949-chr17:17184296..17185001,2	Hela-S3	cervix:
6	chr1:225151942..225154325-chr1:225156559..225160933,3	K562	blood:
7	chr1:225138712..225141214-chr1:225147432..225149142,2	MCF-7	breast:
8	chr1:225148681..225151534-chr1:225153143..225154709,2	K562	blood:
9	chr1:225117101..225117940-chr2:9982915..9983806,2	Hela-S3	cervix:
10	chr1:225117194..225117809-chr12:113772563..113773224,2	NB4	blood:
11	chr1:225116528..225119047-chr1:225122562..225124296,2	K562	blood:
12	chr1:225151942..225154325-chr1:225156559..225160933,3	K562	blood:
13	chr1:225066484..225067986-chr1:225113709..225116590,2	K562	blood:
14	chr1:225119003..225120746-chr1:225122614..225125497,2	MCF-7	breast:
15	chr1:225119750..225122962-chr1:225123939..225127125,5	K562	blood:
16	chr1:225118656..225120791-chr1:225120817..225122470,2	K562	blood:
17	chr1:225117272..225119024-chr1:225143959..225145501,2	K562	blood:
18	chr1:225118805..225120326-chr1:225154882..225156859,2	K562	blood:
19	chr1:225135426..225138299-chr1:225142390..225144172,2	MCF-7	breast:
20	chr1:225133516..225138195-chr1:225140002..225143763,5	K562	blood:
21	chr1:225125254..225128428-chr1:225150698..225154229,3	K562	blood:
22	chr1:225119750..225122962-chr1:225123939..225127125,5	K562	blood:
23	chr1:153539179..153539769-chr1:225117355..225117966,2	Hela-S3	cervix:
24	chr1:225117389..225119047-chr1:225133436..225135148,2	K562	blood:
25	chr1:225122110..225123615-chr1:225123723..225125815,2	K562	blood:
26	chr1:225118656..225120791-chr1:225120817..225122470,2	K562	blood:
27	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
28	chr1:225133403..225135871-chr1:225146349..225149223,2	K562	blood:
29	chr1:225117301..225117958-chr5:140027420..140027937,2	Hela-S3	cervix:
30	chr1:225110317..225111909-chr1:225113611..225115449,2	K562	blood:
31	chr1:225122110..225123615-chr1:225123723..225125815,2	K562	blood:
32	chr1:225117272..225119612-chr1:225143482..225145459,3	K562	blood:
33	chr1:225117129..225118085-chr13:31191178..31192009,2	NB4	blood:
34	chr1:225119003..225120746-chr1:225122614..225125497,2	MCF-7	breast:
35	chr1:225117334..225118220-chr11:72524845..72525840,2	Hela-S3	cervix:
36	chr1:225117317..225117947-chr11:18547900..18548603,2	NB4	blood:
37	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
38	chr1:225117919..225119549-chr1:225136065..225138730,2	K562	blood:
39	chr1:225117903..225119549-chr1:225136065..225137999,2	K562	blood:
40	chr1:225148681..225151534-chr1:225153143..225154709,2	K562	blood:
41	chr1:8014073..8014650-chr1:225117304..225117825,2	Hela-S3	cervix:
42	chr1:225117919..225119549-chr1:225136065..225138730,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-4	chr1:225156461-225157195	NONHSAT009831
2	lnc-CNIH3-4	chr1:225155248-225155285	NONHSAT009831

No data

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island
ENSG00000089060	chromatin interactions
ENSG00000116288	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000132952	chromatin interactions
ENSG00000113141	chromatin interactions
ENSG00000141030	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000264052	chromatin interactions
ENSG00000196754	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000074319	chromatin interactions

Extended variants
information (count: 1585 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2489353	chr1:225114654-225114655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184014648	chr1:225114680-225114681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188031817	chr1:225114712-225114713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548394860	chr1:225114729-225114730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61852096	chr1:225114742-225114743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190552360	chr1:225114743-225114744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2489354	chr1:225114811-225114812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs2501080	chr1:225114823-225114824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs528644513	chr1:225114836-225114837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548695340	chr1:225114839-225114840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147589326	chr1:225114840-225114841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2489355	chr1:225114898-225114899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530694169	chr1:225114902-225114903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550864570	chr1:225114922-225114923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553070980	chr1:225114950-225114951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566224003	chr1:225114967-225114968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60006038	chr1:225114986-225114987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201406872	chr1:225114987-225114988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574607527	chr1:225115019-225115020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201151486	chr1:225115061-225115062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183114038	chr1:225115063-225115064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187046691	chr1:225115125-225115126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2406098	chr1:225115150-225115151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575487344	chr1:225115164-225115165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545827282	chr1:225115186-225115187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565263137	chr1:225115197-225115198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532403012	chr1:225115205-225115206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6426164	chr1:225115206-225115207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs61852097	chr1:225115209-225115210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs566120459	chr1:225115224-225115225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548333579	chr1:225115233-225115234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2406097	chr1:225115234-225115235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs537745768	chr1:225115254-225115255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552622758	chr1:225115280-225115281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6693680	chr1:225115309-225115310	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534572780	chr1:225115335-225115336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148910532	chr1:225115398-225115399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568123388	chr1:225115408-225115409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192935622	chr1:225115419-225115420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144976350	chr1:225115420-225115421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148025495	chr1:225115425-225115426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112764251	chr1:225115506-225115507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557731682	chr1:225115567-225115568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184127320	chr1:225115608-225115609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540977458	chr1:225115609-225115610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559330204	chr1:225115618-225115619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530123183	chr1:225115619-225115620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187865269	chr1:225115621-225115622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542003912	chr1:225115663-225115664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561279618	chr1:225115671-225115672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Acute lymphoblastic leukemia	21098271	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
Developmental delay	21147756	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
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Alzheimer''s disease	22166940	CNVD
micrognathia	21364285	CNVD
Breast cancer	22522925	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	chr1:225110200-225117000	Weak transcription	Gastric	stomach
2	chr1:225110400-225117000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:225110400-225117000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:225110400-225117000	Weak transcription	Pancreas	Pancrea
5	chr1:225110800-225116200	Weak transcription	Liver	Liver
6	chr1:225111600-225117000	Weak transcription	NH-A	brain
7	chr1:225112400-225117000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:225113000-225117000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:225116200-225116800	Enhancers	Liver	Liver
10	chr1:225116800-225117000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:225116800-225117000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:225116800-225117000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:225116800-225117000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:225116800-225117000	Enhancers	Adipose Nuclei	Adipose
15	chr1:225116800-225117000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr1:225116800-225117000	Enhancers	Placenta	Placenta
17	chr1:225116800-225117000	Enhancers	Fetal Thymus	thymus
18	chr1:225116800-225117000	Enhancers	HMEC	breast
19	chr1:225116800-225117000	Active TSS	HUVEC	blood vessel
20	chr1:225116800-225117200	Flanking Active TSS	Liver	Liver
21	chr1:225116800-225118000	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr1:225116800-225118200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:225116800-225118400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr1:225116800-225118400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr1:225116800-225118400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:225116800-225118400	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr1:225116800-225118600	Active TSS	A549	lung
28	chr1:225116800-225118800	Active TSS	Hela-S3	cervix
29	chr1:225117000-225117200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:225117000-225117200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:225117000-225117200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:225117000-225117200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
33	chr1:225117000-225117200	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr1:225117000-225117200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:225117000-225117200	Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr1:225117000-225117200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:225117000-225117200	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr1:225117000-225117200	Active TSS	Fetal Muscle Trunk	muscle
39	chr1:225117000-225117200	Flanking Active TSS	Fetal Muscle Leg	muscle
40	chr1:225117000-225117200	Flanking Active TSS	Gastric	stomach
41	chr1:225117000-225117200	Active TSS	Lung	lung
42	chr1:225117000-225117200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr1:225117000-225117200	Active TSS	Right Atrium	heart
44	chr1:225117000-225117200	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr1:225117000-225117200	Active TSS	Stomach Smooth Muscle	stomach
46	chr1:225117000-225117200	Enhancers	Spleen	Spleen
47	chr1:225117000-225117200	Bivalent Enhancer	Dnd41	blood
48	chr1:225117000-225117200	Flanking Active TSS	K562	blood
49	chr1:225117000-225117200	Flanking Active TSS	NH-A	brain
50	chr1:225117000-225117200	Flanking Active TSS	NHDF-Ad	bronchial

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