Variant report

Variant	esv15701
Chromosome Location	chr1:224096726-224179951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:677)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224124412-224124623	K562	blood:	n/a	n/a
2	ARID3A	chr1:224119208-224119671	K562	blood:	n/a	n/a
3	ATF1	chr1:224119207-224119478	K562	blood:	n/a	n/a
4	BATF	chr1:224179785-224180831	GM12878	blood:	n/a	n/a
5	BATF	chr1:224144651-224145050	GM12878	blood:	n/a	n/a
6	BATF	chr1:224104058-224104261	GM12878	blood:	n/a	n/a
7	BATF	chr1:224100132-224100691	GM12878	blood:	n/a	chr1:224100431-224100442
8	BATF	chr1:224108555-224108855	GM12878	blood:	n/a	chr1:224108835-224108844
9	BATF	chr1:224108598-224108877	GM12878	blood:	n/a	chr1:224108835-224108844
10	BATF	chr1:224100112-224100738	GM12878	blood:	n/a	chr1:224100431-224100442
11	BATF	chr1:224103998-224104234	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:224111240-224111434	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:224108051-224108199	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:224100059-224100720	GM12878	blood:	n/a	chr1:224100434-224100443
15	BCL11A	chr1:224100121-224100579	GM12878	blood:	n/a	chr1:224100434-224100443
16	BCL11A	chr1:224179801-224179949	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:224103937-224104270	GM12878	blood:	n/a	chr1:224104160-224104168
18	BCL11A	chr1:224179744-224180938	GM12878	blood:	n/a	chr1:224180534-224180543 chr1:224180711-224180724 chr1:224180714-224180727
19	BHLHE40	chr1:224112070-224112315	HepG2	liver:	n/a	n/a
20	BHLHE40	chr1:224110721-224110974	HepG2	liver:	n/a	n/a
21	BHLHE40	chr1:224108563-224108836	HepG2	liver:	n/a	n/a
22	CBX3	chr1:224179390-224179770	K562	blood:	n/a	n/a
23	CBX3	chr1:224179867-224180856	K562	blood:	n/a	n/a
24	CCNT2	chr1:224124418-224124640	K562	blood:	n/a	n/a
25	CCNT2	chr1:224119307-224119476	K562	blood:	n/a	n/a
26	CEBPB	chr1:224179718-224180685	K562	blood:	n/a	chr1:224180401-224180409
27	CEBPB	chr1:224119050-224119660	K562	blood:	n/a	n/a
28	CEBPB	chr1:224128087-224128547	K562	blood:	n/a	n/a
29	CEBPB	chr1:224111522-224111543	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:224152616-224152643	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:224149750-224150127	IMR90	lung:	n/a	chr1:224149926-224149937
32	CEBPB	chr1:224140423-224140638	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:224146942-224147108	K562	blood:	n/a	n/a
34	CEBPB	chr1:224119272-224119685	K562	blood:	n/a	n/a
35	CEBPB	chr1:224146909-224147154	K562	blood:	n/a	n/a
36	CEBPD	chr1:224119236-224119796	K562	blood:	n/a	n/a
37	CEBPD	chr1:224124238-224124681	K562	blood:	n/a	n/a
38	CEBPD	chr1:224123228-224123626	K562	blood:	n/a	n/a
39	CHD2	chr1:224123348-224123652	K562	blood:	n/a	n/a
40	CTCF	chr1:224108820-224108970	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr1:224138600-224138750	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:224108580-224108730	GM12865	blood:	n/a	n/a
43	CTCF	chr1:224108644-224108729	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:224108538-224108877	K562	blood:	n/a	n/a
45	CTCF	chr1:224179325-224181033	K562	blood:	n/a	n/a
46	CTCF	chr1:224108580-224108730	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr1:224108665-224108778	K562	blood:	n/a	n/a
48	CTCF	chr1:224108560-224108710	AG04450	lung:	n/a	n/a
49	CTCF	chr1:224108512-224108868	K562	blood:	n/a	n/a
50	CTCF	chr1:224108709-224108747	GM12891	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224179665-224179715	T-47D	breast:	n/a
2	chr1:224177126-224177176	RPTEC	kidney:	n/a
3	chr1:224136349-224136399	HCT-116	colon:	n/a
4	chr1:224133090-224133140	HCF	heart:	n/a
5	chr1:224133090-224133140	HUVEC	blood vessel:	n/a
6	chr1:224179665-224179715	Jurkat	blood:	n/a
7	chr1:224179665-224179715	HRE	kidney:	n/a
8	chr1:224136349-224136399	Caco-2	colon:	n/a
9	chr1:224136349-224136399	BJ	skin:	n/a
10	chr1:224136349-224136399	Jurkat	blood:	n/a
11	chr1:224179665-224179715	GM12892	blood:	n/a
12	chr1:224136349-224136399	HIPEpiC	eye:	n/a
13	chr1:224177126-224177176	SAEC	small airway:	n/a
14	chr1:224179665-224179715	AG10803	skin:	n/a
15	chr1:224133090-224133140	PANC-1	pancreas:	n/a
16	chr1:224133090-224133140	AG10803	skin:	n/a
17	chr1:224136349-224136399	Hepatocyte	liver:	n/a
18	chr1:224179665-224179715	HNPCEpiC	eye:	n/a
19	chr1:224136349-224136399	NHDF-neo	bronchial:	n/a
20	chr1:224133090-224133140	SKMC	muscle:	n/a
21	chr1:224133090-224133140	ovcar-3	ovarian:	n/a
22	chr1:224133090-224133140	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:224177126-224177176	SK-N-SH	brain:	n/a
24	chr1:224136349-224136399	T-47D	breast:	n/a
25	chr1:224179665-224179715	HAEpiC	amniotic membrane:	n/a
26	chr1:224179665-224179715	MCF10A-Er-Src	breast:	n/a
27	chr1:224179665-224179715	SKMC	muscle:	n/a
28	chr1:224133090-224133140	HCPEpiC	choroid plexus:	n/a
29	chr1:224177126-224177176	GM19239	blood:	n/a
30	chr1:224133090-224133140	NHBE	bronchial:	n/a
31	chr1:224133090-224133140	HEK293	kidney:	embryo
32	chr1:224177126-224177176	NB4	blood:	n/a
33	chr1:224179665-224179715	NH-A	brain:	n/a
34	chr1:224136349-224136399	PFSK-1	brain:	n/a
35	chr1:224136349-224136399	HMEC	breast:	n/a
36	chr1:224177126-224177176	GM12891	blood:	n/a
37	chr1:224133090-224133140	U87	brain:	n/a
38	chr1:224177126-224177176	HCM	heart:	n/a
39	chr1:224133090-224133140	MCF-7	breast:	n/a
40	chr1:224133090-224133140	HIPEpiC	eye:	n/a
41	chr1:224177126-224177176	U87	brain:	n/a
42	chr1:224136349-224136399	HCPEpiC	choroid plexus:	n/a
43	chr1:224179665-224179715	SK-N-SH	brain:	n/a
44	chr1:224133090-224133140	HRCEpiC	kidney:	n/a
45	chr1:224177126-224177176	Caco-2	colon:	n/a
46	chr1:224177126-224177176	HCPEpiC	choroid plexus:	n/a
47	chr1:224136349-224136399	GM19239	blood:	n/a
48	chr1:224177126-224177176	ProgFib	skin:	n/a
49	chr1:224136349-224136399	NT2-D1	testis:	n/a
50	chr1:224179665-224179715	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:223887763..223889342-chr1:224178879..224180474,2	K562	blood:
2	chr1:224178905..224181889-chr1:224301318..224303879,2	MCF-7	breast:
3	chr1:224030638..224033175-chr1:224122761..224125405,2	K562	blood:
4	chr1:223900030..223900536-chr1:224108678..224109196,2	K562	blood:
5	chr1:224178733..224180652-chr1:224310129..224312087,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP2-3	chr1:224139722-224139941	NONHSAT009752
2	lnc-TP53BP2-4	chr1:224149779-224150142	NONHSAT009753
3	lnc-TP53BP2-4	chr1:224148701-224148934	NONHSAT009753
4	lnc-TP53BP2-1	chr1:224159276-224159470	XLOC_001223
5	lnc-TP53BP2-6	chr1:224170893-224170987	NONHSAT009756
6	lnc-TP53BP2-6	chr1:224172084-224172141	NONHSAT009757
7	lnc-TP53BP2-6	chr1:224175747-224175856	NONHSAT009756
8	lnc-TP53BP2-4	chr1:224150312-224150411	NONHSAT009754
9	lnc-TP53BP2-6	chr1:224170898-224170987	NONHSAT009757
10	lnc-TP53BP2-4	chr1:224149779-224150042	NONHSAT009754
11	lnc-TP53BP2-6	chr1:224170584-224170818	NONHSAT009757
12	lnc-PARP1-3	chr1:224098433-224099085	expRegAs_chr1_21128_-
13	lnc-TP53BP2-6	chr1:224170456-224170544	NONHSAT009756
14	lnc-TP53BP2-1	chr1:224151308-224152241	XLOC_001223
15	lnc-TP53BP2-6	chr1:224174277-224174342	NONHSAT009756
16	lnc-PARP1-4	chr1:224096672-224097019	expRegAs_chr1_21127_-

No data

Variant related genes	Relation type
ENSG00000232372	TF binding region
ENSG00000243000	TF binding region
ENSG00000185495	TF binding region
ENSG00000272645	TF binding region
CICP5	TF binding region
RNU6-1319P	TF binding region
ENSG00000232372	CpG island
ENSG00000243000	CpG island
ENSG00000185495	CpG island
ENSG00000272645	CpG island
CICP5	CpG island
RNU6-1319P	CpG island
ENSG00000162909	chromatin interactions
ENSG00000143756	chromatin interactions
WNT5B	miRNA target sites
AHCYL2	miRNA target sites

Extended variants
information (count: 1560 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1560 , 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	rs202220497	chr1:224096754-224096755	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs567761949	chr1:224096764-224096765	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs112053357	chr1:224096841-224096842	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs535702389	chr1:224096899-224096900	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs557238553	chr1:224096949-224096950	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs575758997	chr1:224096952-224096953	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs4120673	chr1:224096979-224096980	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs183778672	chr1:224096984-224096985	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs376226239	chr1:224097004-224097005	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs4120672	chr1:224097017-224097018	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs573239908	chr1:224097068-224097069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4653622	chr1:224097069-224097070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186267315	chr1:224097073-224097074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12089517	chr1:224097105-224097106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190733427	chr1:224097111-224097112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542111819	chr1:224097149-224097150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4653621	chr1:224097155-224097156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371216722	chr1:224097173-224097174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4120670	chr1:224097178-224097179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530864514	chr1:224097188-224097189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552073359	chr1:224097240-224097241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200567897	chr1:224097255-224097256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528168535	chr1:224097258-224097259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150267676	chr1:224097259-224097260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4653620	chr1:224097278-224097279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111643173	chr1:224097290-224097291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368871978	chr1:224097292-224097293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542753141	chr1:224097294-224097295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4102659	chr1:224097310-224097311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4102660	chr1:224097351-224097352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3856158	chr1:224097353-224097354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12044552	chr1:224097358-224097359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs9660081	chr1:224097409-224097410	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201247959	chr1:224097415-224097416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2404582	chr1:224097424-224097425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569427725	chr1:224097446-224097447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145803273	chr1:224097463-224097464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187099058	chr1:224097487-224097488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3992031	chr1:224097514-224097515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567058067	chr1:224097596-224097597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551187160	chr1:224097608-224097609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534247229	chr1:224097692-224097693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373851189	chr1:224097704-224097705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12044701	chr1:224097799-224097800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs371226404	chr1:224097810-224097811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574056925	chr1:224097902-224097903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544597602	chr1:224097911-224097912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12044554	chr1:224097980-224097981	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs191551256	chr1:224097982-224097983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546122679	chr1:224097983-224097984	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	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
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	17060936	CNVD
Ewing''s sarcoma	19144156	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224096200-224097400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr1:224097400-224099600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:224097800-224099000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr1:224099000-224100600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:224099600-224101600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr1:224100600-224102000	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr1:224101600-224102000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:224119200-224119600	Enhancers	K562	blood
9	chr1:224135800-224149800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:224136200-224139400	Weak transcription	Fetal Intestine Small	intestine
11	chr1:224136400-224179800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:224136600-224149200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:224137200-224138600	Weak transcription	Fetal Stomach	stomach
14	chr1:224137600-224139200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:224137800-224139400	Weak transcription	Adipose Nuclei	Adipose
16	chr1:224137800-224139400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:224137800-224139400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:224137800-224139400	Weak transcription	Placenta	Placenta
19	chr1:224137800-224139400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr1:224137800-224139400	Weak transcription	Spleen	Spleen
21	chr1:224137800-224160600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:224138000-224139400	Weak transcription	Lung	lung
23	chr1:224138000-224139600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:224138000-224139600	Weak transcription	Ovary	ovary
25	chr1:224138000-224140000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:224138000-224141000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:224138000-224148200	Weak transcription	Liver	Liver
28	chr1:224138000-224162800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:224138000-224163800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:224138000-224170000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:224138000-224179600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:224138200-224149800	Weak transcription	Right Ventricle	heart
33	chr1:224138200-224150400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr1:224138200-224179200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr1:224138200-224179600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr1:224138200-224179600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:224138400-224140800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr1:224138400-224140800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:224138400-224149600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:224138400-224179600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:224138400-224179800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr1:224138600-224141000	Strong transcription	Fetal Stomach	stomach
43	chr1:224138600-224141200	Weak transcription	Gastric	stomach
44	chr1:224138600-224179600	Weak transcription	Fetal Muscle Leg	muscle
45	chr1:224138800-224140000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:224138800-224140000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:224138800-224179800	Weak transcription	Left Ventricle	heart
48	chr1:224139000-224139400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:224139200-224139800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:224139400-224139600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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