Variant report

Variant	esv1834321
Chromosome Location	chr1:169180302-169240975
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	chr1:169219638-169220576	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169209995-169210076	K562	blood:	n/a	n/a
3	ARID3A	chr1:169235297-169235803	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:169240319-169240724	K562	blood:	n/a	n/a
5	ATF1	chr1:169210187-169210271	K562	blood:	n/a	n/a
6	ATF1	chr1:169240334-169240757	K562	blood:	n/a	n/a
7	BHLHE40	chr1:169240319-169240648	K562	blood:	n/a	n/a
8	CEBPB	chr1:169185148-169185442	IMR90	lung:	n/a	chr1:169185313-169185324
9	CEBPB	chr1:169185350-169185379	K562	blood:	n/a	n/a
10	CEBPB	chr1:169180613-169180892	IMR90	lung:	n/a	chr1:169180744-169180757 chr1:169180745-169180756 chr1:169180744-169180757 chr1:169180744-169180755
11	CEBPB	chr1:169185183-169185469	A549	lung:	n/a	chr1:169185313-169185324
12	CEBPB	chr1:169217146-169217217	HepG2	liver:	n/a	chr1:169217167-169217178
13	CEBPB	chr1:169219114-169219471	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:169217062-169217242	IMR90	lung:	n/a	chr1:169217167-169217178
15	CEBPB	chr1:169185167-169185473	HepG2	liver:	n/a	chr1:169185313-169185324
16	CEBPB	chr1:169180642-169180851	HepG2	liver:	n/a	chr1:169180744-169180757 chr1:169180745-169180756 chr1:169180744-169180757 chr1:169180744-169180755
17	CEBPB	chr1:169209637-169210183	HCT-116	colon:	n/a	n/a
18	CEBPB	chr1:169229862-169230008	K562	blood:	n/a	chr1:169229886-169229899 chr1:169229888-169229897 chr1:169229888-169229897 chr1:169229886-169229897 chr1:169229888-169229897 chr1:169229887-169229898 chr1:169229888-169229897
19	CEBPB	chr1:169186176-169186318	A549	lung:	n/a	chr1:169186259-169186270
20	CEBPB	chr1:169240163-169240324	K562	blood:	n/a	chr1:169240208-169240219 chr1:169240208-169240219 chr1:169240206-169240219 chr1:169240206-169240219
21	CEBPB	chr1:169186111-169186334	HepG2	liver:	n/a	chr1:169186259-169186270
22	CEBPB	chr1:169229825-169229981	HepG2	liver:	n/a	chr1:169229886-169229899 chr1:169229888-169229897 chr1:169229888-169229897 chr1:169229886-169229897 chr1:169229888-169229897 chr1:169229887-169229898 chr1:169229888-169229897
23	CEBPB	chr1:169180644-169180884	K562	blood:	n/a	chr1:169180744-169180757 chr1:169180745-169180756 chr1:169180744-169180757 chr1:169180744-169180755
24	CEBPB	chr1:169195001-169195136	HepG2	liver:	n/a	chr1:169195073-169195084
25	CTCF	chr1:169240500-169240650	HVMF	connective:	n/a	n/a
26	CTCF	chr1:169240420-169240570	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:169240585-169240694	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr1:169240552-169240712	HepG2	liver:	n/a	n/a
29	CTCF	chr1:169240561-169240669	GM12878	blood:	n/a	n/a
30	CTCF	chr1:169240565-169240710	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:169240520-169240670	HMF	breast:	n/a	n/a
32	CTCF	chr1:169240520-169240670	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:169205520-169205670	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr1:169240500-169240650	GM12872	blood:	n/a	n/a
35	CTCF	chr1:169240520-169240670	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr1:169240440-169240590	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr1:169240520-169240670	HEK293	kidney:	n/a	n/a
38	CTCF	chr1:169240580-169240730	HPF	lung:	n/a	n/a
39	CTCF	chr1:169240540-169240690	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr1:169240540-169240690	K562	blood:	n/a	n/a
41	CTCF	chr1:169240540-169240690	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:169240540-169240690	AG04450	lung:	n/a	n/a
43	CTCF	chr1:169215445-169215504	Fibrobl	skin:	n/a	n/a
44	CTCF	chr1:169240540-169240690	HPF	lung:	n/a	n/a
45	CTCF	chr1:169240600-169240750	HRE	kidney:	n/a	n/a
46	CTCF	chr1:169240540-169240690	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr1:169240560-169240710	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:169240537-169240716	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:169240581-169240651	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:169240480-169240630	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169187004-169187054	SK-N-MC	brain:	n/a
2	chr1:169187004-169187054	LNCaP	prostate:	n/a
3	chr1:169187004-169187054	AG09309	skin:	n/a
4	chr1:169187004-169187054	HAEpiC	amniotic membrane:	n/a
5	chr1:169187004-169187054	T-47D	breast:	n/a
6	chr1:169187004-169187054	HEEpiC	esophagus:	n/a
7	chr1:169187004-169187054	GM19239	blood:	n/a
8	chr1:169187004-169187054	HEK293	kidney:	embryo
9	chr1:169187004-169187054	SAEC	small airway:	n/a
10	chr1:169187004-169187054	NT2-D1	testis:	n/a
11	chr1:169187004-169187054	SKMC	muscle:	n/a
12	chr1:169187004-169187054	PANC-1	pancreas:	n/a
13	chr1:169187004-169187054	H1-hESC	embryonic stem cell:	embryo
14	chr1:169187004-169187054	Hela-S3	cervix:	n/a
15	chr1:169187004-169187054	U87	brain:	n/a
16	chr1:169187004-169187054	IMR90	lung:	fetal
17	chr1:169187004-169187054	GM12891	blood:	n/a
18	chr1:169187004-169187054	HRPEpiC	eye:	n/a
19	chr1:169187004-169187054	HIPEpiC	eye:	n/a
20	chr1:169187004-169187054	GM12878	blood:	n/a
21	chr1:169187004-169187054	MCF10A-Er-Src	breast:	n/a
22	chr1:169187004-169187054	ECC-1	luminal epithelium:	n/a
23	chr1:169187004-169187054	HRCEpiC	kidney:	n/a
24	chr1:169187004-169187054	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:169187004-169187054	PrEC	prostate:	n/a
26	chr1:169187004-169187054	ProgFib	skin:	n/a
27	chr1:169187004-169187054	NHDF-neo	bronchial:	n/a
28	chr1:169187004-169187054	Jurkat	blood:	n/a
29	chr1:169187004-169187054	NB4	blood:	n/a
30	chr1:169187004-169187054	K562	blood:	n/a
31	chr1:169187004-169187054	MCF-7	breast:	n/a
32	chr1:169187004-169187054	NH-A	brain:	n/a
33	chr1:169187004-169187054	HRE	kidney:	n/a
34	chr1:169187004-169187054	AG10803	skin:	n/a
35	chr1:169187004-169187054	ovcar-3	ovarian:	n/a
36	chr1:169187004-169187054	BJ	skin:	n/a
37	chr1:169187004-169187054	HCM	heart:	n/a
38	chr1:169187004-169187054	Hepatocyte	liver:	n/a
39	chr1:169187004-169187054	RPTEC	kidney:	n/a
40	chr1:169187004-169187054	HUVEC	blood vessel:	n/a
41	chr1:169187004-169187054	A549	lung:	n/a
42	chr1:169187004-169187054	CMK	blood:	n/a
43	chr1:169187004-169187054	AG04450	lung:	fetal
44	chr1:169187004-169187054	HNPCEpiC	eye:	n/a
45	chr1:169187004-169187054	HCF	heart:	n/a
46	chr1:169187004-169187054	BE2_C	brain:	n/a
47	chr1:169187004-169187054	SK-N-SH_RA	brain:	n/a
48	chr1:169187004-169187054	HL-60	blood:	n/a
49	chr1:169187004-169187054	AoSMC	blood vessel:	n/a
50	chr1:169187004-169187054	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169210215..169210976-chr2:173891921..173892590,2	MCF-7	breast:
2	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
3	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
4	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
5	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
6	chr1:169193895..169196797-chr1:169197836..169199358,2	MCF-7	breast:
7	chr1:169192162..169194718-chr1:169212473..169215131,2	K562	blood:
8	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
9	chr1:169193895..169196797-chr1:169197836..169199358,2	MCF-7	breast:
10	chr1:169177420..169179762-chr1:169182344..169184753,2	MCF-7	breast:
11	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
12	chr1:169192162..169194718-chr1:169212473..169215131,2	K562	blood:

Variant related genes	Relation type
NME7	TF binding region
NME7	CpG island

Extended variants
information (count: 2083 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2083 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3766077	chr1:169180302-169180303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114020881	chr1:169180309-169180310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563360300	chr1:169180542-169180543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181893224	chr1:169180546-169180547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552815517	chr1:169180572-169180573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570925269	chr1:169180596-169180597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528805816	chr1:169180605-169180606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12142454	chr1:169180671-169180672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573062989	chr1:169180747-169180748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546959432	chr1:169180812-169180813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10919095	chr1:169180857-169180858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs12089602	chr1:169180898-169180899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs557080818	chr1:169180914-169180915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs36040633	chr1:169180927-169180928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539505611	chr1:169180942-169180943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558731085	chr1:169180981-169180982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116781340	chr1:169181009-169181010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541343160	chr1:169181039-169181040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12139905	chr1:169181069-169181070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564582996	chr1:169181075-169181076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552974458	chr1:169181092-169181093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111383579	chr1:169181096-169181097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541841824	chr1:169181097-169181098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116422067	chr1:169181127-169181128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530641086	chr1:169181168-169181169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146253454	chr1:169181193-169181194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564733283	chr1:169181311-169181312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528663509	chr1:169181374-169181375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142062715	chr1:169181392-169181393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139176683	chr1:169181537-169181538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10800415	chr1:169181553-169181554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs186215028	chr1:169181557-169181558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142479880	chr1:169181609-169181610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111849369	chr1:169181733-169181734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200432387	chr1:169181764-169181765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555460776	chr1:169181767-169181768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61806243	chr1:169181769-169181770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201027825	chr1:169181772-169181773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74414612	chr1:169181773-169181774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376494634	chr1:169181774-169181775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35973200	chr1:169181834-169181835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12748602	chr1:169181836-169181837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368293506	chr1:169181837-169181838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571226352	chr1:169181847-169181848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71121740	chr1:169181857-169181858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575503763	chr1:169181896-169181897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12121395	chr1:169181912-169181913	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs190723693	chr1:169181967-169181968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12403013	chr1:169182010-169182011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535715854	chr1:169182028-169182029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169130400-169195200	Weak transcription	Pancreas	Pancrea
2	chr1:169163600-169184000	Weak transcription	Ovary	ovary
3	chr1:169167800-169186800	Weak transcription	Primary T cells from cord blood	blood
4	chr1:169168000-169183800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:169171600-169184000	Weak transcription	Fetal Intestine Small	intestine
6	chr1:169172400-169183800	Weak transcription	Brain Germinal Matrix	brain
7	chr1:169172400-169207600	Weak transcription	Esophagus	oesophagus
8	chr1:169172600-169227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:169173200-169202000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:169173600-169183800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:169176600-169206200	Weak transcription	Aorta	Aorta
12	chr1:169177400-169207400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:169178600-169191400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:169180000-169210000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:169180600-169206200	Weak transcription	Left Ventricle	heart
16	chr1:169181200-169184000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:169181400-169185400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:169181800-169184400	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr1:169182000-169184600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr1:169182000-169185400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:169182000-169201000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:169182600-169183800	Weak transcription	Primary B cells from cord blood	blood
23	chr1:169182800-169192000	Weak transcription	Small Intestine	intestine
24	chr1:169182800-169205400	Weak transcription	Adipose Nuclei	Adipose
25	chr1:169183400-169183800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:169183600-169183800	Weak transcription	Fetal Stomach	stomach
27	chr1:169183600-169184000	Weak transcription	Gastric	stomach
28	chr1:169183600-169187200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:169183800-169184000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:169183800-169184600	Strong transcription	Primary B cells from cord blood	blood
31	chr1:169183800-169184600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr1:169183800-169184600	ZNF genes & repeats	Brain Germinal Matrix	brain
33	chr1:169183800-169184800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:169183800-169184800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:169184000-169184200	Strong transcription	Fetal Intestine Small	intestine
36	chr1:169184000-169184200	ZNF genes & repeats	Fetal Stomach	stomach
37	chr1:169184000-169184200	ZNF genes & repeats	Gastric	stomach
38	chr1:169184000-169184400	ZNF genes & repeats	Lung	lung
39	chr1:169184000-169184400	ZNF genes & repeats	Dnd41	blood
40	chr1:169184000-169184600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:169184000-169184800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
42	chr1:169184000-169184800	ZNF genes & repeats	Ovary	ovary
43	chr1:169184000-169198800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:169184200-169184600	Strong transcription	Fetal Stomach	stomach
45	chr1:169184200-169185000	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr1:169184200-169185600	Weak transcription	Gastric	stomach
47	chr1:169184400-169206200	Weak transcription	Lung	lung
48	chr1:169184600-169185400	Weak transcription	Primary B cells from cord blood	blood
49	chr1:169184600-169185800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:169184600-169186000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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