Variant report

Variant	nsv873226
Chromosome Location	chr1:225347689-225555602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225396825-225397387	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225531377-225531662	K562	blood:	n/a	n/a
3	ARID3A	chr1:225416534-225417017	HepG2	liver:	n/a	n/a
4	ATF1	chr1:225522856-225523015	K562	blood:	n/a	n/a
5	ATF1	chr1:225368725-225368728	K562	blood:	n/a	n/a
6	ATF1	chr1:225539395-225539510	K562	blood:	n/a	n/a
7	ATF2	chr1:225438070-225438415	GM12878	blood:	n/a	n/a
8	BATF	chr1:225438165-225438534	GM12878	blood:	n/a	n/a
9	BATF	chr1:225534936-225535219	GM12878	blood:	n/a	n/a
10	BATF	chr1:225438147-225438493	GM12878	blood:	n/a	n/a
11	BATF	chr1:225534970-225535263	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:225438166-225438412	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:225438111-225438466	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:225506659-225507037	K562	blood:	n/a	n/a
15	BHLHE40	chr1:225438084-225438466	GM12878	blood:	n/a	n/a
16	CBX3	chr1:225365330-225365566	K562	blood:	n/a	n/a
17	CBX3	chr1:225468343-225468607	HCT-116	colon:	n/a	n/a
18	CBX3	chr1:225365321-225365563	K562	blood:	n/a	n/a
19	CBX3	chr1:225468317-225468636	HCT-116	colon:	n/a	n/a
20	CBX3	chr1:225468328-225468669	K562	blood:	n/a	n/a
21	CBX3	chr1:225468298-225468601	K562	blood:	n/a	n/a
22	CCNT2	chr1:225468943-225469050	K562	blood:	n/a	n/a
23	CEBPB	chr1:225479132-225479159	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:225552141-225552561	ECC-1	luminal epithelium:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
25	CEBPB	chr1:225516786-225517098	HepG2	liver:	n/a	chr1:225516936-225516947 chr1:225516938-225516947
26	CEBPB	chr1:225552157-225552436	MCF-7	breast:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
27	CEBPB	chr1:225417884-225418049	HepG2	liver:	n/a	chr1:225417940-225417951
28	CEBPB	chr1:225552110-225552541	K562	blood:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
29	CEBPB	chr1:225552171-225552544	A549	lung:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
30	CEBPB	chr1:225552154-225552531	IMR90	lung:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
31	CEBPB	chr1:225516755-225517131	Hela-S3	cervix:	n/a	chr1:225516936-225516947 chr1:225516938-225516947
32	CEBPB	chr1:225547888-225548062	A549	lung:	n/a	chr1:225547989-225548000
33	CEBPB	chr1:225447251-225447411	HepG2	liver:	n/a	chr1:225447297-225447308
34	CEBPB	chr1:225552181-225552523	Hela-S3	cervix:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
35	CEBPB	chr1:225552154-225552520	A549	lung:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
36	CEBPB	chr1:225552090-225552479	HCT-116	colon:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
37	CEBPB	chr1:225548440-225548640	K562	blood:	n/a	n/a
38	CEBPB	chr1:225552157-225552530	H1-hESC	embryonic stem cell:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
39	CEBPB	chr1:225552174-225552585	ECC-1	luminal epithelium:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
40	CEBPB	chr1:225464505-225464691	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:225552179-225552460	K562	blood:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
42	CEBPB	chr1:225466364-225466580	HepG2	liver:	n/a	chr1:225466481-225466494 chr1:225466481-225466494 chr1:225466483-225466494 chr1:225466481-225466492
43	CEBPB	chr1:225547872-225548141	HepG2	liver:	n/a	chr1:225547989-225548000
44	CEBPB	chr1:225553340-225553366	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:225412593-225412887	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:225547843-225548075	IMR90	lung:	n/a	chr1:225547989-225548000
47	CEBPB	chr1:225417850-225417972	IMR90	lung:	n/a	chr1:225417940-225417951
48	CEBPB	chr1:225552155-225552528	HepG2	liver:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348
49	CEBPB	chr1:225542497-225542704	A549	lung:	n/a	chr1:225542613-225542626 chr1:225542613-225542624 chr1:225542613-225542626 chr1:225542615-225542626 chr1:225542615-225542626
50	CEBPB	chr1:225552249-225552397	HepG2	liver:	n/a	chr1:225552337-225552350 chr1:225552337-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348 chr1:225552339-225552348

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225427173-225427223	Jurkat	blood:	n/a
2	chr1:225427173-225427223	GM12891	blood:	n/a
3	chr1:225427173-225427223	AG09309	skin:	n/a
4	chr1:225427173-225427223	U87	brain:	n/a
5	chr1:225427173-225427223	T-47D	breast:	n/a
6	chr1:225427173-225427223	HRCEpiC	kidney:	n/a
7	chr1:225427173-225427223	NB4	blood:	n/a
8	chr1:225427173-225427223	ProgFib	skin:	n/a
9	chr1:225427173-225427223	CMK	blood:	n/a
10	chr1:225427173-225427223	RPTEC	kidney:	n/a
11	chr1:225427173-225427223	HNPCEpiC	eye:	n/a
12	chr1:225427173-225427223	BJ	skin:	n/a
13	chr1:225427173-225427223	HEEpiC	esophagus:	n/a
14	chr1:225427173-225427223	HAEpiC	amniotic membrane:	n/a
15	chr1:225427173-225427223	HIPEpiC	eye:	n/a
16	chr1:225427173-225427223	HMEC	breast:	n/a
17	chr1:225427173-225427223	Hela-S3	cervix:	n/a
18	chr1:225427173-225427223	NT2-D1	testis:	n/a
19	chr1:225427173-225427223	HCF	heart:	n/a
20	chr1:225427173-225427223	HCT-116	colon:	n/a
21	chr1:225427173-225427223	AG10803	skin:	n/a
22	chr1:225427173-225427223	PANC-1	pancreas:	n/a
23	chr1:225427173-225427223	NH-A	brain:	n/a
24	chr1:225427173-225427223	HCPEpiC	choroid plexus:	n/a
25	chr1:225427173-225427223	IMR90	lung:	fetal
26	chr1:225427173-225427223	SAEC	small airway:	n/a
27	chr1:225427173-225427223	K562	blood:	n/a
28	chr1:225427173-225427223	BE2_C	brain:	n/a
29	chr1:225427173-225427223	Caco-2	colon:	n/a
30	chr1:225427173-225427223	HRPEpiC	eye:	n/a
31	chr1:225427173-225427223	NHBE	bronchial:	n/a
32	chr1:225427173-225427223	HepG2	liver:	n/a
33	chr1:225427173-225427223	SKMC	muscle:	n/a
34	chr1:225427173-225427223	HUVEC	blood vessel:	n/a
35	chr1:225427173-225427223	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:225427173-225427223	PrEC	prostate:	n/a
37	chr1:225427173-225427223	HCM	heart:	n/a
38	chr1:225427173-225427223	SK-N-SH	brain:	n/a
39	chr1:225427173-225427223	NHDF-neo	bronchial:	n/a
40	chr1:225427173-225427223	H1-hESC	embryonic stem cell:	embryo
41	chr1:225427173-225427223	MCF10A-Er-Src	breast:	n/a
42	chr1:225427173-225427223	GM19239	blood:	n/a
43	chr1:225427173-225427223	A549	lung:	n/a
44	chr1:225427173-225427223	AoSMC	blood vessel:	n/a
45	chr1:225427173-225427223	HRE	kidney:	n/a
46	chr1:225427173-225427223	MCF-7	breast:	n/a
47	chr1:225427173-225427223	Hepatocyte	liver:	n/a
48	chr1:225427173-225427223	GM12892	blood:	n/a
49	chr1:225427173-225427223	HL-60	blood:	n/a
50	chr1:225427173-225427223	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:225528499..225531078-chr1:225532986..225535776,3	K562	blood:
2	chr1:225549684..225551436-chr1:225553572..225555467,2	K562	blood:
3	chr1:225540074..225543141-chr1:225544972..225548275,3	K562	blood:
4	chr1:225507669..225509816-chr1:225510822..225512373,3	K562	blood:
5	chr1:225539242..225541399-chr1:225541845..225544252,2	MCF-7	breast:
6	chr1:225547542..225550580-chr1:225551460..225555926,4	MCF-7	breast:
7	chr1:225488601..225490317-chr1:225494794..225496298,2	MCF-7	breast:
8	chr1:225488601..225490317-chr1:225494794..225496298,2	MCF-7	breast:
9	chr1:225528499..225531078-chr1:225532986..225535776,3	K562	blood:
10	chr1:225539242..225541399-chr1:225541845..225544252,2	MCF-7	breast:
11	chr1:225537288..225539034-chr1:225551951..225554490,2	K562	blood:
12	chr1:225506556..225507373-chr1:225531091..225531759,2	MCF-7	breast:
13	chr1:225507669..225509816-chr1:225510822..225512373,3	K562	blood:
14	chr1:225540074..225543141-chr1:225544972..225548275,3	K562	blood:
15	chr1:225487478..225490427-chr1:225503792..225505643,2	K562	blood:
16	chr1:225506454..225506954-chr1:225625445..225626402,2	MCF-7	breast:
17	chr1:225528499..225531078-chr1:225533837..225535776,2	K562	blood:
18	chr1:225506556..225507373-chr1:225531091..225531759,2	MCF-7	breast:
19	chr1:225465995..225468148-chr1:225470406..225472141,2	K562	blood:
20	chr1:225537534..225539602-chr1:225550916..225553451,2	K562	blood:
21	chr1:225549684..225551436-chr1:225553572..225555467,2	K562	blood:
22	chr1:225552393..225554542-chr1:225560951..225562986,2	K562	blood:
23	chr1:225549565..225551972-chr1:225560136..225561675,2	K562	blood:
24	chr1:225528499..225531078-chr1:225533837..225535776,2	K562	blood:
25	chr1:225487478..225490427-chr1:225503792..225505643,2	K562	blood:
26	chr1:225465995..225468148-chr1:225470406..225472141,2	K562	blood:
27	chr1:225040443..225041021-chr1:225531064..225531583,2	MCF-7	breast:
28	chr1:225547542..225550580-chr1:225551460..225555926,4	MCF-7	breast:
29	chr1:225537288..225539034-chr1:225551951..225554490,2	K562	blood:
30	chr1:225540127..225543141-chr1:225544972..225548486,4	K562	blood:
31	chr1:225540127..225543141-chr1:225544972..225548486,4	K562	blood:
32	chr1:225537534..225539602-chr1:225550916..225553451,2	K562	blood:

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island

Extended variants
information (count: 5082 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5082 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16844400	chr1:225347689-225347690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs36079806	chr1:225347814-225347815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374354921	chr1:225347954-225347955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567998615	chr1:225347959-225347960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146464815	chr1:225347961-225347962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564370866	chr1:225347979-225347980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548526434	chr1:225348018-225348019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563530398	chr1:225348181-225348182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180819903	chr1:225348191-225348192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186261477	chr1:225348246-225348247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111608571	chr1:225348304-225348305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530504508	chr1:225348311-225348312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140923623	chr1:225348320-225348321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538786552	chr1:225348357-225348358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377667855	chr1:225348369-225348370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142046885	chr1:225348383-225348384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191884062	chr1:225348410-225348411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151144331	chr1:225348448-225348449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183414722	chr1:225348472-225348473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564878615	chr1:225348499-225348500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570053346	chr1:225348519-225348520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550449386	chr1:225348521-225348522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12143049	chr1:225348599-225348600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558293927	chr1:225348620-225348621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576756230	chr1:225348653-225348654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540786709	chr1:225348656-225348657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140360142	chr1:225348718-225348719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570552831	chr1:225348737-225348738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187263073	chr1:225348764-225348765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574691307	chr1:225348789-225348790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138792633	chr1:225348792-225348793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113525266	chr1:225348830-225348831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34405198	chr1:225348843-225348844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542007479	chr1:225348848-225348849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35114401	chr1:225348849-225348850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190594832	chr1:225348872-225348873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530759773	chr1:225348881-225348882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546058916	chr1:225348898-225348899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373485716	chr1:225348916-225348917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78626289	chr1:225348920-225348921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116040229	chr1:225348930-225348931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182378838	chr1:225348932-225348933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527302677	chr1:225348978-225348979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547488680	chr1:225349093-225349094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138092042	chr1:225349154-225349155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566397439	chr1:225349162-225349163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34778535	chr1:225349193-225349194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570207369	chr1:225349247-225349248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111900033	chr1:225349278-225349279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12736406	chr1:225349289-225349290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225301800-225355800	Weak transcription	Pancreas	Pancrea
2	chr1:225322000-225356000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:225326400-225355800	Weak transcription	Ovary	ovary
4	chr1:225332800-225356000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:225338200-225355600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:225344000-225356200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:225353400-225355800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:225354800-225357200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:225355400-225356000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:225355400-225356600	Weak transcription	Liver	Liver
11	chr1:225355400-225356800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:225355600-225356800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
13	chr1:225355800-225356400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:225355800-225356800	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr1:225355800-225356800	ZNF genes & repeats	Ovary	ovary
16	chr1:225355800-225356800	ZNF genes & repeats	Pancreas	Pancrea
17	chr1:225356000-225356200	Weak transcription	Thymus	Thymus
18	chr1:225356000-225356400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:225356000-225356800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:225356000-225356800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:225356000-225356800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
22	chr1:225356000-225356800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
23	chr1:225356000-225356800	ZNF genes & repeats	Fetal Intestine Large	intestine
24	chr1:225356200-225356400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:225356200-225356600	ZNF genes & repeats	Thymus	Thymus
26	chr1:225356200-225356800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:225356200-225356800	ZNF genes & repeats	Fetal Stomach	stomach
28	chr1:225356400-225357600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:225356600-225356800	ZNF genes & repeats	Liver	Liver
30	chr1:225356800-225357000	Weak transcription	Liver	Liver
31	chr1:225356800-225357200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:225356800-225357200	Weak transcription	Fetal Intestine Large	intestine
33	chr1:225356800-225365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:225356800-225365200	Weak transcription	Pancreas	Pancrea
35	chr1:225365200-225365600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:225365200-225366000	ZNF genes & repeats	Pancreas	Pancrea
37	chr1:225365400-225366000	ZNF genes & repeats	Liver	Liver
38	chr1:225366000-225372400	Weak transcription	Pancreas	Pancrea
39	chr1:225368400-225373200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:225370000-225372400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:225370200-225370800	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr1:225373800-225374800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:225374800-225375200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:225375200-225378400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:225375800-225377000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:225378400-225380200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:225379400-225381600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:225380200-225386000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:225384200-225384600	Weak transcription	Liver	Liver
50	chr1:225389000-225389600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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