Variant report

Variant	nsv549264
Chromosome Location	chr1:225304971-225476025
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:440)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225416534-225417017	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225396825-225397387	HepG2	liver:	n/a	n/a
3	ATF1	chr1:225368725-225368728	K562	blood:	n/a	n/a
4	ATF2	chr1:225438070-225438415	GM12878	blood:	n/a	n/a
5	BATF	chr1:225438165-225438534	GM12878	blood:	n/a	n/a
6	BATF	chr1:225438147-225438493	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:225438111-225438466	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:225438166-225438412	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:225438084-225438466	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:225325986-225326003	HepG2	liver:	n/a	n/a
11	CBX3	chr1:225365330-225365566	K562	blood:	n/a	n/a
12	CBX3	chr1:225468343-225468607	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:225365321-225365563	K562	blood:	n/a	n/a
14	CBX3	chr1:225468328-225468669	K562	blood:	n/a	n/a
15	CBX3	chr1:225468298-225468601	K562	blood:	n/a	n/a
16	CBX3	chr1:225468317-225468636	HCT-116	colon:	n/a	n/a
17	CCNT2	chr1:225468943-225469050	K562	blood:	n/a	n/a
18	CEBPB	chr1:225417884-225418049	HepG2	liver:	n/a	chr1:225417940-225417951
19	CEBPB	chr1:225466364-225466580	HepG2	liver:	n/a	chr1:225466481-225466494 chr1:225466481-225466494 chr1:225466483-225466494 chr1:225466481-225466492
20	CEBPB	chr1:225424526-225424624	A549	lung:	n/a	n/a
21	CEBPB	chr1:225412593-225412887	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:225308863-225309125	A549	lung:	n/a	chr1:225308986-225308997
23	CEBPB	chr1:225308825-225309165	Hela-S3	cervix:	n/a	chr1:225308986-225308997
24	CEBPB	chr1:225308834-225309187	ECC-1	luminal epithelium:	n/a	chr1:225308986-225308997
25	CEBPB	chr1:225323924-225323961	A549	lung:	n/a	n/a
26	CEBPB	chr1:225396821-225397186	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:225459947-225460000	A549	lung:	n/a	n/a
28	CEBPB	chr1:225447251-225447411	HepG2	liver:	n/a	chr1:225447297-225447308
29	CEBPB	chr1:225308815-225309171	MCF-7	breast:	n/a	chr1:225308986-225308997
30	CEBPB	chr1:225308816-225309180	K562	blood:	n/a	chr1:225308986-225308997
31	CEBPB	chr1:225417850-225417972	IMR90	lung:	n/a	chr1:225417940-225417951
32	CEBPB	chr1:225308815-225309121	H1-hESC	embryonic stem cell:	n/a	chr1:225308986-225308997
33	CEBPB	chr1:225308810-225309179	A549	lung:	n/a	chr1:225308986-225308997
34	CEBPB	chr1:225308818-225309168	IMR90	lung:	n/a	chr1:225308986-225308997
35	CEBPB	chr1:225308838-225309244	A549	lung:	n/a	chr1:225308986-225308997
36	CEBPB	chr1:225464505-225464691	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:225308807-225309166	HepG2	liver:	n/a	chr1:225308986-225308997
38	CEBPZ	chr1:225416674-225416952	HepG2	liver:	n/a	n/a
39	CHD2	chr1:225438181-225438501	GM12878	blood:	n/a	n/a
40	CTCF	chr1:225370560-225370710	NHEK	skin:	n/a	n/a
41	CTCF	chr1:225440960-225441110	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:225440980-225441130	GM12864	blood:	n/a	n/a
43	CTCF	chr1:225441100-225441250	GM12871	blood:	n/a	n/a
44	CTCF	chr1:225440960-225441110	GM12865	blood:	n/a	n/a
45	CTCF	chr1:225440980-225441130	K562	blood:	n/a	n/a
46	CTCF	chr1:225461069-225461111	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr1:225441040-225441190	GM06990	blood:	n/a	n/a
48	CTCF	chr1:225441000-225441150	GM06990	blood:	n/a	n/a
49	CTCF	chr1:225440980-225441130	BE2_C	brain:	n/a	n/a
50	CTCF	chr1:225441080-225441230	GM12872	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225427173-225427223	MCF-7	breast:	n/a
2	chr1:225332226-225332276	SK-N-MC	brain:	n/a
3	chr1:225332226-225332276	SK-N-SH	brain:	n/a
4	chr1:225332226-225332276	HAEpiC	amniotic membrane:	n/a
5	chr1:225427173-225427223	AG04450	lung:	fetal
6	chr1:225332226-225332276	NB4	blood:	n/a
7	chr1:225427173-225427223	PrEC	prostate:	n/a
8	chr1:225332226-225332276	HRPEpiC	eye:	n/a
9	chr1:225427173-225427223	HIPEpiC	eye:	n/a
10	chr1:225332226-225332276	GM12892	blood:	n/a
11	chr1:225427173-225427223	IMR90	lung:	fetal
12	chr1:225332226-225332276	AG09309	skin:	n/a
13	chr1:225332226-225332276	CMK	blood:	n/a
14	chr1:225427173-225427223	ECC-1	luminal epithelium:	n/a
15	chr1:225332226-225332276	HMEC	breast:	n/a
16	chr1:225427173-225427223	GM19239	blood:	n/a
17	chr1:225332226-225332276	AG04450	lung:	fetal
18	chr1:225332226-225332276	T-47D	breast:	n/a
19	chr1:225427173-225427223	GM12892	blood:	n/a
20	chr1:225332226-225332276	LNCaP	prostate:	n/a
21	chr1:225427173-225427223	HCF	heart:	n/a
22	chr1:225427173-225427223	HRPEpiC	eye:	n/a
23	chr1:225332226-225332276	NHDF-neo	bronchial:	n/a
24	chr1:225427173-225427223	Jurkat	blood:	n/a
25	chr1:225332226-225332276	H1-hESC	embryonic stem cell:	embryo
26	chr1:225332226-225332276	GM06990	blood:	n/a
27	chr1:225332226-225332276	NHBE	bronchial:	n/a
28	chr1:225427173-225427223	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:225332226-225332276	ECC-1	luminal epithelium:	n/a
30	chr1:225332226-225332276	HCM	heart:	n/a
31	chr1:225332226-225332276	GM12891	blood:	n/a
32	chr1:225332226-225332276	HIPEpiC	eye:	n/a
33	chr1:225427173-225427223	HRCEpiC	kidney:	n/a
34	chr1:225332226-225332276	PFSK-1	brain:	n/a
35	chr1:225332226-225332276	SAEC	small airway:	n/a
36	chr1:225332226-225332276	MCF-7	breast:	n/a
37	chr1:225427173-225427223	GM12878	blood:	n/a
38	chr1:225427173-225427223	RPTEC	kidney:	n/a
39	chr1:225332226-225332276	BJ	skin:	n/a
40	chr1:225332226-225332276	HCT-116	colon:	n/a
41	chr1:225427173-225427223	HCM	heart:	n/a
42	chr1:225332226-225332276	SK-N-SH_RA	brain:	n/a
43	chr1:225332226-225332276	Hela-S3	cervix:	n/a
44	chr1:225427173-225427223	GM06990	blood:	n/a
45	chr1:225332226-225332276	AG10803	skin:	n/a
46	chr1:225332226-225332276	HepG2	liver:	n/a
47	chr1:225427173-225427223	K562	blood:	n/a
48	chr1:225332226-225332276	GM12878	blood:	n/a
49	chr1:225427173-225427223	ProgFib	skin:	n/a
50	chr1:225427173-225427223	BJ	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:225339059..225340673-chr1:225341407..225343124,2	K562	blood:
2	chr1:225339059..225340673-chr1:225341407..225343124,2	K562	blood:
3	chr1:225465995..225468148-chr1:225470406..225472141,2	K562	blood:
4	chr1:225114949..225117606-chr1:225342545..225344625,2	K562	blood:
5	chr1:225465995..225468148-chr1:225470406..225472141,2	K562	blood:
6	chr1:225326089..225328657-chr1:225330172..225331750,2	K562	blood:
7	chr1:225326089..225328657-chr1:225330172..225331750,2	K562	blood:

No data

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

Extended variants
information (count: 4529 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4529 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs995634	chr1:225304971-225304972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546072434	chr1:225304980-225304981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184911736	chr1:225305040-225305041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202179577	chr1:225305059-225305060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574536078	chr1:225305071-225305072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12027336	chr1:225305074-225305075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546812882	chr1:225305096-225305097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74147112	chr1:225305135-225305136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530111375	chr1:225305137-225305138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529554634	chr1:225305181-225305182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556855369	chr1:225305217-225305218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10915781	chr1:225305220-225305221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs563694106	chr1:225305317-225305318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531116785	chr1:225305397-225305398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12080062	chr1:225305529-225305530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549310089	chr1:225305541-225305542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200749774	chr1:225305564-225305565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs16843988	chr1:225305572-225305573	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534342495	chr1:225305594-225305595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546248311	chr1:225305609-225305610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568161689	chr1:225305618-225305619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375097364	chr1:225305627-225305628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557121413	chr1:225305651-225305652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74147113	chr1:225305681-225305682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113651787	chr1:225305691-225305692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138839705	chr1:225305721-225305722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573153132	chr1:225305734-225305735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376541385	chr1:225305741-225305742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541461192	chr1:225305778-225305779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553060262	chr1:225305779-225305780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189345006	chr1:225305816-225305817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192334371	chr1:225305818-225305819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61213216	chr1:225305828-225305829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185529308	chr1:225305851-225305852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147496206	chr1:225306001-225306002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189433171	chr1:225306011-225306012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564460058	chr1:225306015-225306016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182087464	chr1:225306075-225306076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs16843997	chr1:225306092-225306093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567917208	chr1:225306096-225306097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186018738	chr1:225306132-225306133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189217606	chr1:225306158-225306159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148502978	chr1:225306165-225306166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548909164	chr1:225306188-225306189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16844005	chr1:225306199-225306200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557957303	chr1:225306206-225306207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201573388	chr1:225306218-225306219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566791247	chr1:225306220-225306221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377574195	chr1:225306224-225306225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534248627	chr1:225306242-225306243	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:213 , 50 per page) page: 1 2 3 4 5

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	chr1:225307200-225307400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:225307200-225308400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr1:225307200-225308600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:225308600-225310200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:225309800-225313000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:225310400-225315400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:225311600-225312800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:225311600-225315400	Weak transcription	Fetal Intestine Large	intestine
14	chr1:225311800-225312200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:225311800-225313200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
16	chr1:225311800-225313600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
17	chr1:225311800-225314000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:225312000-225312600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:225312000-225313200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
20	chr1:225312000-225313600	ZNF genes & repeats	Liver	Liver
21	chr1:225312200-225312400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:225312400-225313000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:225312600-225313200	ZNF genes & repeats	Ovary	ovary
24	chr1:225312800-225313200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:225313000-225314400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:225313200-225315400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:225313200-225315800	Weak transcription	Ovary	ovary
28	chr1:225322000-225356000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:225323400-225326200	Weak transcription	Ovary	ovary
30	chr1:225324000-225325600	Weak transcription	Fetal Intestine Small	intestine
31	chr1:225325400-225326000	Weak transcription	Gastric	stomach
32	chr1:225325400-225326200	Enhancers	Fetal Muscle Leg	muscle
33	chr1:225325600-225326400	Enhancers	Fetal Muscle Trunk	muscle
34	chr1:225325600-225326600	Strong transcription	Fetal Intestine Small	intestine
35	chr1:225326000-225326400	ZNF genes & repeats	Gastric	stomach
36	chr1:225326200-225326400	ZNF genes & repeats	Ovary	ovary
37	chr1:225326400-225327400	Weak transcription	Gastric	stomach
38	chr1:225326400-225355800	Weak transcription	Ovary	ovary
39	chr1:225326600-225336200	Weak transcription	Fetal Intestine Small	intestine
40	chr1:225327400-225327600	Enhancers	Gastric	stomach
41	chr1:225330800-225331000	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr1:225331000-225339200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr1:225332600-225332800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
44	chr1:225332800-225356000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:225333800-225334200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:225334000-225334600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr1:225334000-225334600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr1:225334000-225334600	Enhancers	Fetal Muscle Leg	muscle
49	chr1:225334200-225334600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr1:225334200-225334600	Enhancers	Fetal Muscle Trunk	muscle

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