Variant report

Variant	nsv871740
Chromosome Location	chr1:98165091-98322379
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	ATF2	chr1:98256657-98257260	GM12878	blood:	n/a	n/a
2	BATF	chr1:98256785-98257057	GM12878	blood:	n/a	n/a
3	BATF	chr1:98314987-98315181	GM12878	blood:	n/a	n/a
4	BCLAF1	chr1:98256717-98257173	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:98286119-98286347	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:98293557-98293863	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:98286097-98286281	HepG2	liver:	n/a	n/a
8	BRCA1	chr1:98315427-98316172	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr1:98286063-98286327	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
11	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694
12	CEBPB	chr1:98208137-98208487	IMR90	lung:	n/a	chr1:98208316-98208327
13	CEBPB	chr1:98208209-98208432	H1-hESC	embryonic stem cell:	n/a	chr1:98208316-98208327
14	CEBPB	chr1:98208142-98208499	A549	lung:	n/a	chr1:98208316-98208327
15	CEBPB	chr1:98177429-98177798	HepG2	liver:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
16	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
17	CEBPB	chr1:98315476-98315890	IMR90	lung:	n/a	chr1:98315683-98315694
18	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
19	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
20	CEBPB	chr1:98177430-98177801	IMR90	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
21	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
22	CEBPB	chr1:98198657-98198872	IMR90	lung:	n/a	chr1:98198701-98198714
23	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
24	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
25	CEBPB	chr1:98192995-98193291	IMR90	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
26	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:98243986-98244310	IMR90	lung:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
28	CEBPB	chr1:98208214-98208462	Hela-S3	cervix:	n/a	chr1:98208316-98208327
29	CEBPB	chr1:98193045-98193294	HepG2	liver:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
30	CEBPB	chr1:98177451-98177785	H1-hESC	embryonic stem cell:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
31	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
32	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
33	CEBPB	chr1:98252463-98252539	A549	lung:	n/a	n/a
34	CEBPB	chr1:98244033-98244278	K562	blood:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
35	CEBPB	chr1:98243965-98244299	HepG2	liver:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
36	CEBPB	chr1:98193010-98193283	A549	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
37	CEBPB	chr1:98177451-98177762	Hela-S3	cervix:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
38	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
39	CEBPB	chr1:98244025-98244225	A549	lung:	n/a	chr1:98244134-98244145 chr1:98244136-98244147 chr1:98244134-98244147 chr1:98244136-98244145
40	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
41	CEBPB	chr1:98208154-98208479	HepG2	liver:	n/a	chr1:98208316-98208327
42	CEBPB	chr1:98228781-98228989	HepG2	liver:	n/a	chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228931-98228942 chr1:98228933-98228942 chr1:98228933-98228944
43	CEBPB	chr1:98177450-98177788	K562	blood:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
44	CEBPB	chr1:98236073-98236275	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:98177432-98177781	A549	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
46	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
47	CEBPB	chr1:98221656-98222027	IMR90	lung:	n/a	chr1:98221861-98221870
48	CEBPB	chr1:98288531-98288718	A549	lung:	n/a	n/a
49	CEBPB	chr1:98211520-98211827	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221

No.	Distal block	Cell Line	Cell type
1	chr1:98228606..98230942-chr1:98231366..98234177,2	K562	blood:
2	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
3	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:
4	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
5	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
6	chr1:98276910..98277431-chr11:65769065..65769690,2	Hela-S3	cervix:
7	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
8	chr1:98232688..98235381-chr1:98240146..98242077,2	MCF-7	breast:
9	chr1:98228606..98230942-chr1:98231366..98234177,2	K562	blood:
10	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
11	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPPR5.1-4	chr1:98229394-98229587	l_97_chr1:98213107-98217461
2	lnc-SNX7-2	chr1:98262771-98262851	NR_046591
3	lnc-SNX7-2	chr1:98262521-98262628	ENSG00000235777.1
4	lnc-LPPR5.1-4	chr1:98217399-98217461	l_97_chr1:98213107-98217461
5	lnc-SNX7-11	chr1:98321131-98322381	NONHSAT004723
6	lnc-SNX7-2	chr1:98263024-98263424	ENSG00000235777.1
7	lnc-LPPR5.1-4	chr1:98213403-98213506	l_97_chr1:98213107-98217461
8	lnc-LPPR5.1-4	chr1:98233060-98233679	l_97_chr1:98213107-98217461
9	lnc-LPPR5.1-4	chr1:98213108-98213244	l_97_chr1:98213107-98217461
10	lnc-SNX7-2	chr1:98263024-98263622	ENSG00000235777.1
11	lnc-SNX7-2	chr1:98262771-98262851	ENSG00000235777.1
12	lnc-SNX7-12	chr1:98240225-98240582	NONHSAT004719
13	lnc-SNX7-2	chr1:98262477-98262628	NR_046591
14	lnc-LPPR5.1-4	chr1:98227401-98227713	l_97_chr1:98213107-98217461
15	lnc-SNX7-2	chr1:98262477-98262851	ENSG00000235777.1
16	lnc-SNX7-2	chr1:98263024-98263607	NR_046591

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DPYD	hsa-miR-124-3p	chr1:98185550-98185569

Variant related genes	Relation type
ENSG00000270911	TF binding region
DPYD	TF binding region
ENSG00000230718	TF binding region
DPYD-AS2	TF binding region
ENSG00000175376	chromatin interactions
ENSG00000175334	chromatin interactions
ENSG00000230718	chromatin interactions
FXR1	miRNA target sites

Extended variants
information (count: 5557 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5557 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2297595	chr1:98165091-98165092	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368970772	chr1:98165098-98165099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs202011255	chr1:98165107-98165108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375466035	chr1:98165114-98165115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551616997	chr1:98165125-98165126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370276860	chr1:98165136-98165137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202132918	chr1:98165152-98165153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571622473	chr1:98165171-98165172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575955756	chr1:98165186-98165187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534372130	chr1:98165190-98165191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115896193	chr1:98165212-98165213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564492010	chr1:98165214-98165215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78176710	chr1:98165218-98165219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547060118	chr1:98165227-98165228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560574633	chr1:98165231-98165232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569536577	chr1:98165240-98165241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78682297	chr1:98165248-98165249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549617407	chr1:98165257-98165258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547650921	chr1:98165283-98165284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187733077	chr1:98165300-98165301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538514772	chr1:98165348-98165349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116406928	chr1:98165455-98165456	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs112348418	chr1:98165477-98165478	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs571217782	chr1:98165505-98165506	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs192067883	chr1:98165517-98165518	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs553413212	chr1:98165521-98165522	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs183965152	chr1:98165529-98165530	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs143256347	chr1:98165573-98165574	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs369324335	chr1:98165579-98165580	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs556943007	chr1:98165613-98165614	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs187527495	chr1:98165631-98165632	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs576194077	chr1:98165649-98165650	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs192055416	chr1:98165667-98165668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs567881430	chr1:98165701-98165702	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs184179217	chr1:98165703-98165704	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs146677753	chr1:98165720-98165721	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540267690	chr1:98165736-98165737	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs187091787	chr1:98165771-98165772	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs375623291	chr1:98165789-98165790	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs140233266	chr1:98165814-98165815	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563048413	chr1:98165851-98165852	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145566496	chr1:98165884-98165885	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191543014	chr1:98165898-98165899	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536337338	chr1:98165925-98165926	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148050023	chr1:98165939-98165940	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140841334	chr1:98165953-98165954	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150147594	chr1:98165991-98165992	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566990364	chr1:98166010-98166011	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535930447	chr1:98166122-98166123	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184493678	chr1:98166144-98166145	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98130800-98171800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr1:98136200-98188800	Weak transcription	Left Ventricle	heart
3	chr1:98141600-98165800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr1:98141800-98166000	Weak transcription	Brain Hippocampus Middle	brain
5	chr1:98141800-98185400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:98143600-98165800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:98144000-98165400	Weak transcription	Brain Substantia Nigra	brain
8	chr1:98144000-98176600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:98144200-98165800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:98144200-98166800	Weak transcription	Osteobl	bone
11	chr1:98146000-98165400	Weak transcription	HMEC	breast
12	chr1:98146400-98166800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr1:98146800-98166000	Weak transcription	Adipose Nuclei	Adipose
14	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr1:98152400-98166000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr1:98152600-98165800	Weak transcription	NHLF	lung
17	chr1:98153400-98187800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr1:98153600-98165200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:98153600-98165200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:98153600-98165600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:98153600-98167000	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:98153600-98167600	Weak transcription	Ovary	ovary
23	chr1:98155200-98167400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:98157200-98175800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:98157400-98168600	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr1:98157600-98165200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:98159800-98165200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:98160000-98167000	Weak transcription	NHDF-Ad	bronchial
29	chr1:98160200-98183200	Weak transcription	Primary T cells from cord blood	blood
30	chr1:98160400-98182800	Weak transcription	Primary B cells from cord blood	blood
31	chr1:98163200-98185400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr1:98164400-98166000	Strong transcription	Liver	Liver
33	chr1:98164800-98165200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:98164800-98165600	Strong transcription	Dnd41	blood
35	chr1:98164800-98165800	Strong transcription	Primary hematopoietic stem cells	blood
36	chr1:98165000-98166200	Strong transcription	HSMM	muscle
37	chr1:98165200-98165800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:98165200-98165800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:98165200-98166000	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr1:98165200-98166000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:98165400-98165600	ZNF genes & repeats	Brain Substantia Nigra	brain
42	chr1:98165600-98166000	ZNF genes & repeats	Dnd41	blood
43	chr1:98165600-98167400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:98165800-98166000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:98165800-98166200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:98165800-98166200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
47	chr1:98165800-98180200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:98166000-98166200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:98166000-98166200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:98166000-98166200	ZNF genes & repeats	Adipose Nuclei	Adipose

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