Variant report

Variant	nsv546870
Chromosome Location	chr1:98253405-98336823
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	BACH1	chr1:98330283-98330429	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:98256785-98257057	GM12878	blood:	n/a	n/a
4	BATF	chr1:98314987-98315181	GM12878	blood:	n/a	n/a
5	BCLAF1	chr1:98256717-98257173	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	BHLHE40	chr1:98286119-98286347	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:98315427-98316172	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:98286063-98286327	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
12	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221
13	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
15	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
16	CEBPB	chr1:98288531-98288718	A549	lung:	n/a	n/a
17	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
18	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694
19	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
20	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
21	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
22	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
23	CEBPB	chr1:98299523-98299768	IMR90	lung:	n/a	chr1:98299621-98299632
24	CEBPB	chr1:98315544-98315841	HCT-116	colon:	n/a	chr1:98315683-98315694
25	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
26	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
27	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
28	CEBPB	chr1:98315476-98315890	IMR90	lung:	n/a	chr1:98315683-98315694
29	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
30	CHD2	chr1:98315502-98315865	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr1:98293520-98293730	GM12878	blood:	n/a	n/a
32	CREB1	chr1:98293481-98293885	GM12878	blood:	n/a	n/a
33	CREB1	chr1:98293440-98293909	GM12878	blood:	n/a	n/a
34	CTCF	chr1:98286117-98286295	MCF-7	breast:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
35	CTCF	chr1:98286120-98286270	NHDF-neo	bronchial:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
36	CTCF	chr1:98286120-98286270	HPAF	blood vessel:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
37	CTCF	chr1:98286169-98286219	ProgFib	skin:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
38	CTCF	chr1:98285968-98286401	A549	lung:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
39	CTCF	chr1:98265309-98265397	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:98292540-98292690	BE2_C	brain:	n/a	n/a
41	CTCF	chr1:98286180-98286330	GM12865	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
42	CTCF	chr1:98286140-98286290	HEK293	kidney:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
43	CTCF	chr1:98331831-98331880	GM20000	blood:	n/a	n/a
44	CTCF	chr1:98286140-98286290	AG04449	skin:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
45	CTCF	chr1:98285988-98286390	IMR90	lung:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
46	CTCF	chr1:98262554-98262581	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr1:98286100-98286250	NHEK	skin:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
48	CTCF	chr1:98286060-98286210	NB4	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
49	CTCF	chr1:98286097-98286302	LNCaP	prostate:	n/a	chr1:98286198-98286206 chr1:98286188-98286209
50	CTCF	chr1:98286120-98286270	GM12864	blood:	n/a	chr1:98286198-98286206 chr1:98286188-98286209

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
2	chr1:98336448-98336498	AG09319	gingival:	n/a
3	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
4	chr1:98336448-98336498	AG09319	gingival:	n/a
5	chr1:98336448-98336498	HL-60	blood:	n/a
6	chr1:98336448-98336498	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:98336448-98336498	HRE	kidney:	n/a
8	chr1:98336448-98336498	Hela-S3	cervix:	n/a
9	chr1:98336448-98336498	U87	brain:	n/a
10	chr1:98336448-98336498	AG10803	skin:	n/a
11	chr1:98336448-98336498	HEK293	kidney:	embryo
12	chr1:98336448-98336498	HCF	heart:	n/a
13	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
14	chr1:98336448-98336498	HNPCEpiC	eye:	n/a
15	chr1:98336448-98336498	HMEC	breast:	n/a
16	chr1:98336448-98336498	NHDF-neo	bronchial:	n/a
17	chr1:98336448-98336498	AG09309	skin:	n/a
18	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
19	chr1:98336448-98336498	AG04450	lung:	fetal
20	chr1:98336448-98336498	SAEC	small airway:	n/a
21	chr1:98336448-98336498	Caco-2	colon:	n/a
22	chr1:98336448-98336498	SK-N-SH_RA	brain:	n/a
23	chr1:98336448-98336498	SK-N-SH	brain:	n/a
24	chr1:98336448-98336498	T-47D	breast:	n/a
25	chr1:98336448-98336498	AG04449	skin:	fetal
26	chr1:98336448-98336498	PFSK-1	brain:	n/a
27	chr1:98336448-98336498	BJ	skin:	n/a
28	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a
29	chr1:98336448-98336498	HCT-116	colon:	n/a
30	chr1:98336448-98336498	LNCaP	prostate:	n/a
31	chr1:98336448-98336498	IMR90	lung:	fetal
32	chr1:98336448-98336498	GM12878	blood:	n/a
33	chr1:98336448-98336498	K562	blood:	n/a
34	chr1:98336448-98336498	PANC-1	pancreas:	n/a
35	chr1:98336448-98336498	Jurkat	blood:	n/a
36	chr1:98336448-98336498	HIPEpiC	eye:	n/a
37	chr1:98336448-98336498	SKMC	muscle:	n/a
38	chr1:98336448-98336498	HRCEpiC	kidney:	n/a
39	chr1:98336448-98336498	RPTEC	kidney:	n/a
40	chr1:98336448-98336498	GM12892	blood:	n/a
41	chr1:98336448-98336498	A549	lung:	n/a
42	chr1:98336448-98336498	NB4	blood:	n/a
43	chr1:98336448-98336498	NH-A	brain:	n/a
44	chr1:98336448-98336498	BE2_C	brain:	n/a
45	chr1:98336448-98336498	SK-N-MC	brain:	n/a
46	chr1:98336448-98336498	ProgFib	skin:	n/a
47	chr1:98336448-98336498	GM12891	blood:	n/a
48	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
49	chr1:98336448-98336498	H1-hESC	embryonic stem cell:	embryo
50	chr1:98336448-98336498	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
2	chr1:98276910..98277431-chr11:65769065..65769690,2	Hela-S3	cervix:
3	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
4	chr1:98268724..98270842-chr1:98273200..98275102,2	K562	blood:
5	chr1:98277100..98278650-chr1:98293087..98294811,2	K562	blood:
6	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX7-2	chr1:98263024-98263622	ENSG00000235777.1
2	lnc-SNX7-2	chr1:98263024-98263607	NR_046591
3	lnc-SNX7-2	chr1:98262771-98262851	ENSG00000235777.1
4	lnc-SNX7-2	chr1:98262477-98262851	ENSG00000235777.1
5	lnc-SNX7-2	chr1:98263024-98263424	ENSG00000235777.1
6	lnc-SNX7-2	chr1:98262771-98262851	NR_046591
7	lnc-SNX7-2	chr1:98262521-98262628	ENSG00000235777.1
8	lnc-SNX7-2	chr1:98262477-98262628	NR_046591
9	lnc-SNX7-11	chr1:98321131-98322381	NONHSAT004723

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

Extended variants
information (count: 2890 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2890 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7527085	chr1:98253405-98253406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527896269	chr1:98253408-98253409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75613058	chr1:98253445-98253446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548062607	chr1:98253466-98253467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192555492	chr1:98253472-98253473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146417950	chr1:98253477-98253478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549540915	chr1:98253491-98253492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569655652	chr1:98253507-98253508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61786605	chr1:98253510-98253511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs149122914	chr1:98253513-98253514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558240520	chr1:98253534-98253535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571865046	chr1:98253537-98253538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572873157	chr1:98253541-98253542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534555119	chr1:98253563-98253564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79806559	chr1:98253586-98253587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375010589	chr1:98253588-98253589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17117176	chr1:98253617-98253618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542983540	chr1:98253622-98253623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368522145	chr1:98253630-98253631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10747485	chr1:98253666-98253667	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs576397774	chr1:98253674-98253675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552345593	chr1:98253687-98253688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545476365	chr1:98253688-98253689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75696555	chr1:98253703-98253704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527883889	chr1:98253715-98253716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10747486	chr1:98253738-98253739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs142219537	chr1:98253740-98253741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530302740	chr1:98253781-98253782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550466432	chr1:98253887-98253888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564080872	chr1:98253890-98253891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs151196452	chr1:98253892-98253893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538633148	chr1:98253895-98253896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114394933	chr1:98253972-98253973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140255907	chr1:98253977-98253978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534496477	chr1:98253992-98253993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34146407	chr1:98254005-98254006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs36060250	chr1:98254015-98254016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150223964	chr1:98254033-98254034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139113812	chr1:98254034-98254035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560313010	chr1:98254037-98254038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536911873	chr1:98254075-98254076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60121289	chr1:98254090-98254091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576310031	chr1:98254095-98254096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141629569	chr1:98254097-98254098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115784638	chr1:98254128-98254129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572606905	chr1:98254187-98254188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35415616	chr1:98254196-98254197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147045931	chr1:98254229-98254230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185565998	chr1:98254244-98254245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138289533	chr1:98254279-98254280	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:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98177200-98254600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:98183600-98279600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:98204000-98256600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:98204200-98257000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:98207000-98254800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr1:98228400-98255200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr1:98231200-98257800	Weak transcription	Small Intestine	intestine
8	chr1:98238600-98256600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:98240200-98256800	Weak transcription	NHDF-Ad	bronchial
10	chr1:98240200-98262400	Weak transcription	Fetal Lung	lung
11	chr1:98240400-98309800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:98240600-98256800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr1:98241800-98256800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:98242200-98255400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:98242200-98256600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:98242200-98291600	Weak transcription	Dnd41	blood
17	chr1:98243000-98257800	Weak transcription	Psoas Muscle	Psoas
18	chr1:98243400-98272600	Weak transcription	Liver	Liver
19	chr1:98243600-98258000	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:98248000-98256600	Weak transcription	Primary T cells from cord blood	blood
21	chr1:98248600-98262400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:98248600-98310600	Weak transcription	Primary B cells from cord blood	blood
23	chr1:98250800-98264000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr1:98252200-98254000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:98253000-98256400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:98253000-98262600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:98254000-98254400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr1:98254400-98255600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr1:98254600-98258000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr1:98254800-98257800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr1:98254800-98258600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:98255000-98258400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:98255200-98255800	Enhancers	HUVEC	blood vessel
34	chr1:98255200-98256200	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr1:98255400-98255600	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr1:98255400-98255800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:98255400-98256000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr1:98255400-98256200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:98255400-98258400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr1:98255600-98255800	Enhancers	GM12878-XiMat	blood
41	chr1:98255600-98256400	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr1:98255600-98256800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr1:98255800-98256600	Weak transcription	GM12878-XiMat	blood
44	chr1:98255800-98310800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:98256000-98256400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:98256200-98256600	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:98256400-98257200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr1:98256400-98257800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:98256400-98264000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr1:98256600-98257000	Enhancers	Primary neutrophils fromperipheralblood	blood

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