Variant report

Variant	nsv524461
Chromosome Location	chr1:225304331-225347689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:225325986-225326003	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:225308807-225309166	HepG2	liver:	n/a	chr1:225308986-225308997
3	CEBPB	chr1:225308810-225309179	A549	lung:	n/a	chr1:225308986-225308997
4	CEBPB	chr1:225308818-225309168	IMR90	lung:	n/a	chr1:225308986-225308997
5	CEBPB	chr1:225308825-225309165	Hela-S3	cervix:	n/a	chr1:225308986-225308997
6	CEBPB	chr1:225308816-225309180	K562	blood:	n/a	chr1:225308986-225308997
7	CEBPB	chr1:225323924-225323961	A549	lung:	n/a	n/a
8	CEBPB	chr1:225308834-225309187	ECC-1	luminal epithelium:	n/a	chr1:225308986-225308997
9	CEBPB	chr1:225308863-225309125	A549	lung:	n/a	chr1:225308986-225308997
10	CEBPB	chr1:225308838-225309244	A549	lung:	n/a	chr1:225308986-225308997
11	CEBPB	chr1:225308815-225309121	H1-hESC	embryonic stem cell:	n/a	chr1:225308986-225308997
12	CEBPB	chr1:225308815-225309171	MCF-7	breast:	n/a	chr1:225308986-225308997
13	CTCF	chr1:225305820-225305970	K562	blood:	n/a	n/a
14	CTCF	chr1:225334180-225334330	GM12878	blood:	n/a	n/a
15	CTCF	chr1:225321964-225322021	GM13976	blood:	n/a	n/a
16	CTCF	chr1:225313940-225314090	GM12869	blood:	n/a	n/a
17	CTCF	chr1:225323780-225323854	GM10248	blood:	n/a	n/a
18	CTCF	chr1:225306490-225306571	LNCaP	prostate:	n/a	n/a
19	E2F4	chr1:225304587-225304757	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr1:225339256-225339366	MCF10A-Er-Src	breast:	n/a	n/a
21	FAM48A	chr1:225310110-225310285	GM12878	blood:	n/a	n/a
22	FOS	chr1:225307039-225307270	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:225307088-225307345	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:225307024-225307322	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:225343988-225344311	HUVEC	blood vessel:	n/a	chr1:225344282-225344293 chr1:225344281-225344288 chr1:225344281-225344289
26	FOS	chr1:225307016-225307353	MCF10A-Er-Src	breast:	n/a	n/a
27	GATA2	chr1:225343941-225344303	HUVEC	blood vessel:	n/a	chr1:225344195-225344205
28	GATA2	chr1:225307800-225308274	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr1:225334466-225334504	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr1:225311097-225311114	SH-SY5Y	brain:	n/a	n/a
31	JUN	chr1:225307169-225307347	K562	blood:	n/a	n/a
32	JUND	chr1:225339440-225339614	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAFF	chr1:225319647-225319880	K562	blood:	n/a	n/a
34	MAFF	chr1:225319606-225319930	HepG2	liver:	n/a	n/a
35	MAFK	chr1:225337078-225337153	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAFK	chr1:225329559-225329676	HepG2	liver:	n/a	n/a
37	MAFK	chr1:225319726-225319851	Hela-S3	cervix:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
38	MAFK	chr1:225319620-225319912	HepG2	liver:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
39	MAFK	chr1:225319756-225319790	H1-hESC	embryonic stem cell:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
40	MAFK	chr1:225329508-225329730	HepG2	liver:	n/a	n/a
41	MAFK	chr1:225319646-225319924	IMR90	lung:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
42	MAFK	chr1:225319596-225319941	HepG2	liver:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
43	MAFK	chr1:225319653-225319868	K562	blood:	n/a	chr1:225319775-225319786 chr1:225319774-225319788
44	NFYA	chr1:225333094-225333207	GM12878	blood:	n/a	n/a
45	POLR2A	chr1:225343957-225344390	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr1:225343944-225344398	HL-60	blood:	n/a	n/a
47	POLR2A	chr1:225305744-225305776	K562	blood:	n/a	n/a
48	POLR2A	chr1:225306373-225306498	K562	blood:	n/a	n/a
49	POLR2A	chr1:225307079-225307367	H1-neurons	neurons:	n/a	n/a
50	POLR2A	chr1:225329542-225329596	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225332226-225332276	GM19239	blood:	n/a
2	chr1:225332226-225332276	HCF	heart:	n/a
3	chr1:225332226-225332276	PFSK-1	brain:	n/a
4	chr1:225332226-225332276	SAEC	small airway:	n/a
5	chr1:225332226-225332276	IMR90	lung:	fetal
6	chr1:225332226-225332276	GM06990	blood:	n/a
7	chr1:225332226-225332276	NHDF-neo	bronchial:	n/a
8	chr1:225332226-225332276	HCM	heart:	n/a
9	chr1:225332226-225332276	Hepatocyte	liver:	n/a
10	chr1:225332226-225332276	U87	brain:	n/a
11	chr1:225332226-225332276	NT2-D1	testis:	n/a
12	chr1:225332226-225332276	SKMC	muscle:	n/a
13	chr1:225332226-225332276	RPTEC	kidney:	n/a
14	chr1:225332226-225332276	LNCaP	prostate:	n/a
15	chr1:225332226-225332276	HRPEpiC	eye:	n/a
16	chr1:225332226-225332276	NH-A	brain:	n/a
17	chr1:225332226-225332276	HNPCEpiC	eye:	n/a
18	chr1:225332226-225332276	Caco-2	colon:	n/a
19	chr1:225332226-225332276	MCF-7	breast:	n/a
20	chr1:225332226-225332276	AoSMC	blood vessel:	n/a
21	chr1:225332226-225332276	H1-hESC	embryonic stem cell:	embryo
22	chr1:225332226-225332276	HMEC	breast:	n/a
23	chr1:225332226-225332276	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:225332226-225332276	GM12892	blood:	n/a
25	chr1:225332226-225332276	HepG2	liver:	n/a
26	chr1:225332226-225332276	BE2_C	brain:	n/a
27	chr1:225332226-225332276	AG10803	skin:	n/a
28	chr1:225332226-225332276	AG09309	skin:	n/a
29	chr1:225332226-225332276	NHBE	bronchial:	n/a
30	chr1:225332226-225332276	HCPEpiC	choroid plexus:	n/a
31	chr1:225332226-225332276	HEEpiC	esophagus:	n/a
32	chr1:225332226-225332276	HAEpiC	amniotic membrane:	n/a
33	chr1:225332226-225332276	ovcar-3	ovarian:	n/a
34	chr1:225332226-225332276	HUVEC	blood vessel:	n/a
35	chr1:225332226-225332276	PrEC	prostate:	n/a
36	chr1:225332226-225332276	A549	lung:	n/a
37	chr1:225332226-225332276	SK-N-SH	brain:	n/a
38	chr1:225332226-225332276	ProgFib	skin:	n/a
39	chr1:225332226-225332276	BJ	skin:	n/a
40	chr1:225332226-225332276	AG09319	gingival:	n/a
41	chr1:225332226-225332276	HIPEpiC	eye:	n/a
42	chr1:225332226-225332276	HL-60	blood:	n/a
43	chr1:225332226-225332276	PANC-1	pancreas:	n/a
44	chr1:225332226-225332276	SK-N-MC	brain:	n/a
45	chr1:225332226-225332276	HCT-116	colon:	n/a
46	chr1:225332226-225332276	AG04450	lung:	fetal
47	chr1:225332226-225332276	K562	blood:	n/a
48	chr1:225332226-225332276	MCF10A-Er-Src	breast:	n/a
49	chr1:225332226-225332276	CMK	blood:	n/a
50	chr1:225332226-225332276	HRE	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:225339059..225340673-chr1:225341407..225343124,2	K562	blood:
2	chr1:225326089..225328657-chr1:225330172..225331750,2	K562	blood:
3	chr1:225326089..225328657-chr1:225330172..225331750,2	K562	blood:
4	chr1:225114949..225117606-chr1:225342545..225344625,2	K562	blood:
5	chr1:225339059..225340673-chr1:225341407..225343124,2	K562	blood:

No data

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island
ENSG00000185842	chromatin interactions

Extended variants
information (count: 1495 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16843950	chr1:225304331-225304332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556306824	chr1:225304345-225304346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112770283	chr1:225304372-225304373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563625519	chr1:225304391-225304392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76052697	chr1:225304411-225304412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543853179	chr1:225304430-225304431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565238200	chr1:225304443-225304444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532655879	chr1:225304504-225304505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547958144	chr1:225304527-225304528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559585664	chr1:225304566-225304567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562760727	chr1:225304593-225304594	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369109130	chr1:225304647-225304648	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs78489669	chr1:225304659-225304660	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548475657	chr1:225304661-225304662	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs570350710	chr1:225304669-225304670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs16843956	chr1:225304670-225304671	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551767903	chr1:225304678-225304679	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376366101	chr1:225304689-225304690	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369949726	chr1:225304695-225304696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs570157232	chr1:225304767-225304768	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs535614834	chr1:225304768-225304769	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs75520248	chr1:225304846-225304847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552683560	chr1:225304847-225304848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74147111	chr1:225304867-225304868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150370472	chr1:225304894-225304895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371683093	chr1:225304925-225304926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556843147	chr1:225304942-225304943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs995634	chr1:225304971-225304972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs546072434	chr1:225304980-225304981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184911736	chr1:225305040-225305041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202179577	chr1:225305059-225305060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574536078	chr1:225305071-225305072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12027336	chr1:225305074-225305075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546812882	chr1:225305096-225305097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74147112	chr1:225305135-225305136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530111375	chr1:225305137-225305138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529554634	chr1:225305181-225305182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556855369	chr1:225305217-225305218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10915781	chr1:225305220-225305221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563694106	chr1:225305317-225305318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531116785	chr1:225305397-225305398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12080062	chr1:225305529-225305530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs549310089	chr1:225305541-225305542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200749774	chr1:225305564-225305565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16843988	chr1:225305572-225305573	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534342495	chr1:225305594-225305595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546248311	chr1:225305609-225305610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568161689	chr1:225305618-225305619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375097364	chr1:225305627-225305628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557121413	chr1:225305651-225305652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Breast cancer	22522925	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225275600-225312600	Weak transcription	Ovary	ovary
2	chr1:225298000-225311800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:225299800-225314200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:225300400-225311800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:225301800-225355800	Weak transcription	Pancreas	Pancrea
6	chr1:225303000-225304800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:225307200-225307400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:225307200-225308400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:225307200-225308600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:225308600-225310200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:225309800-225313000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:225310400-225315400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:225311600-225312800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:225311600-225315400	Weak transcription	Fetal Intestine Large	intestine
15	chr1:225311800-225312200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:225311800-225313200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
17	chr1:225311800-225313600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr1:225311800-225314000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:225312000-225312600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:225312000-225313200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
21	chr1:225312000-225313600	ZNF genes & repeats	Liver	Liver
22	chr1:225312200-225312400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:225312400-225313000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:225312600-225313200	ZNF genes & repeats	Ovary	ovary
25	chr1:225312800-225313200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:225313000-225314400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:225313200-225315400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:225313200-225315800	Weak transcription	Ovary	ovary
29	chr1:225322000-225356000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:225323400-225326200	Weak transcription	Ovary	ovary
31	chr1:225324000-225325600	Weak transcription	Fetal Intestine Small	intestine
32	chr1:225325400-225326000	Weak transcription	Gastric	stomach
33	chr1:225325400-225326200	Enhancers	Fetal Muscle Leg	muscle
34	chr1:225325600-225326400	Enhancers	Fetal Muscle Trunk	muscle
35	chr1:225325600-225326600	Strong transcription	Fetal Intestine Small	intestine
36	chr1:225326000-225326400	ZNF genes & repeats	Gastric	stomach
37	chr1:225326200-225326400	ZNF genes & repeats	Ovary	ovary
38	chr1:225326400-225327400	Weak transcription	Gastric	stomach
39	chr1:225326400-225355800	Weak transcription	Ovary	ovary
40	chr1:225326600-225336200	Weak transcription	Fetal Intestine Small	intestine
41	chr1:225327400-225327600	Enhancers	Gastric	stomach
42	chr1:225330800-225331000	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr1:225331000-225339200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr1:225332600-225332800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr1:225332800-225356000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr1:225333800-225334200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:225334000-225334600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:225334000-225334600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr1:225334000-225334600	Enhancers	Fetal Muscle Leg	muscle
50	chr1:225334200-225334600	Enhancers	H1 Cell Line	embryonic stem cell

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