Variant report

Variant	nsv3587
Chromosome Location	chr1:172836950-172882218
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:245)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:172876361-172876744	K562	blood:	n/a	n/a
2	ATF1	chr1:172856442-172856553	K562	blood:	n/a	n/a
3	ATF1	chr1:172855308-172855333	K562	blood:	n/a	n/a
4	ATF1	chr1:172872021-172872182	K562	blood:	n/a	n/a
5	ATF2	chr1:172864186-172864788	GM12878	blood:	n/a	n/a
6	ATF2	chr1:172852690-172853073	GM12878	blood:	n/a	n/a
7	BACH1	chr1:172875973-172876843	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:172876127-172877001	K562	blood:	n/a	n/a
9	BATF	chr1:172840281-172840662	GM12878	blood:	n/a	chr1:172840462-172840472 chr1:172840457-172840468
10	BATF	chr1:172864098-172864695	GM12878	blood:	n/a	n/a
11	BATF	chr1:172852651-172852942	GM12878	blood:	n/a	chr1:172852860-172852868
12	BATF	chr1:172863394-172863859	GM12878	blood:	n/a	chr1:172863651-172863662
13	BATF	chr1:172863436-172863763	GM12878	blood:	n/a	chr1:172863651-172863662
14	BATF	chr1:172840190-172840674	GM12878	blood:	n/a	chr1:172840462-172840472 chr1:172840457-172840468
15	BATF	chr1:172862371-172862698	GM12878	blood:	n/a	chr1:172862570-172862579
16	BATF	chr1:172852564-172853306	GM12878	blood:	n/a	chr1:172852860-172852868
17	BCL11A	chr1:172852612-172853031	GM12878	blood:	n/a	chr1:172852863-172852872
18	BCL3	chr1:172864829-172865434	A549	lung:	n/a	chr1:172865396-172865405 chr1:172865395-172865404
19	BHLHE40	chr1:172852739-172852910	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:172876550-172876685	K562	blood:	n/a	n/a
21	BHLHE40	chr1:172863484-172863709	GM12878	blood:	n/a	n/a
22	BRCA1	chr1:172864879-172865281	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:172856612-172856626	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr1:172862446-172863101	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr1:172875813-172876860	K562	blood:	n/a	n/a
26	CBX3	chr1:172854415-172855752	HCT-116	colon:	n/a	chr1:172854921-172854932
27	CBX3	chr1:172866616-172867337	HCT-116	colon:	n/a	n/a
28	CBX3	chr1:172875832-172876992	HCT-116	colon:	n/a	n/a
29	CBX3	chr1:172854510-172855672	HCT-116	colon:	n/a	chr1:172854921-172854932
30	CBX3	chr1:172881982-172882241	K562	blood:	n/a	n/a
31	CBX3	chr1:172876304-172876699	K562	blood:	n/a	n/a
32	CBX3	chr1:172882063-172882370	K562	blood:	n/a	n/a
33	CBX3	chr1:172866689-172867423	HCT-116	colon:	n/a	n/a
34	CBX3	chr1:172840000-172840906	HCT-116	colon:	n/a	n/a
35	CBX3	chr1:172875760-172877424	HCT-116	colon:	n/a	n/a
36	CBX3	chr1:172878575-172879548	HCT-116	colon:	n/a	n/a
37	CBX3	chr1:172864805-172865335	HCT-116	colon:	n/a	n/a
38	CBX3	chr1:172881738-172882827	HCT-116	colon:	n/a	n/a
39	CBX3	chr1:172839990-172840927	HCT-116	colon:	n/a	n/a
40	CCNT2	chr1:172876466-172876717	K562	blood:	n/a	n/a
41	CEBPB	chr1:172871962-172873124	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:172879141-172879327	K562	blood:	n/a	chr1:172879232-172879243
43	CEBPB	chr1:172878651-172879572	HCT-116	colon:	n/a	chr1:172879232-172879243
44	CEBPB	chr1:172879041-172879431	A549	lung:	n/a	chr1:172879232-172879243
45	CEBPB	chr1:172854450-172855724	HCT-116	colon:	n/a	n/a
46	CEBPB	chr1:172879054-172879408	K562	blood:	n/a	chr1:172879232-172879243
47	CEBPB	chr1:172871389-172871698	A549	lung:	n/a	chr1:172871528-172871541 chr1:172871528-172871539
48	CEBPB	chr1:172854401-172855812	HCT-116	colon:	n/a	n/a
49	CEBPB	chr1:172864925-172865256	A549	lung:	n/a	n/a
50	CEBPB	chr1:172878438-172879658	HCT-116	colon:	n/a	chr1:172879232-172879243

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:172863499-172863549	HRPEpiC	eye:	n/a
2	chr1:172863499-172863549	HRPEpiC	eye:	n/a
3	chr1:172852813-172852863	RPTEC	kidney:	n/a
4	chr1:172864347-172864397	SK-N-SH_RA	brain:	n/a
5	chr1:172879281-172879331	HUVEC	blood vessel:	n/a
6	chr1:172863499-172863549	AG09319	gingival:	n/a
7	chr1:172879281-172879331	HIPEpiC	eye:	n/a
8	chr1:172852813-172852863	NB4	blood:	n/a
9	chr1:172852813-172852863	HIPEpiC	eye:	n/a
10	chr1:172863499-172863549	HRE	kidney:	n/a
11	chr1:172863499-172863549	H1-hESC	embryonic stem cell:	embryo
12	chr1:172879281-172879331	GM19239	blood:	n/a
13	chr1:172852813-172852863	HRPEpiC	eye:	n/a
14	chr1:172852813-172852863	HMEC	breast:	n/a
15	chr1:172852813-172852863	Jurkat	blood:	n/a
16	chr1:172863499-172863549	ProgFib	skin:	n/a
17	chr1:172879281-172879331	SAEC	small airway:	n/a
18	chr1:172863499-172863549	HepG2	liver:	n/a
19	chr1:172864347-172864397	SKMC	muscle:	n/a
20	chr1:172863499-172863549	HCF	heart:	n/a
21	chr1:172864347-172864397	HIPEpiC	eye:	n/a
22	chr1:172864347-172864397	SAEC	small airway:	n/a
23	chr1:172879281-172879331	HRE	kidney:	n/a
24	chr1:172852813-172852863	NHBE	bronchial:	n/a
25	chr1:172863499-172863549	PANC-1	pancreas:	n/a
26	chr1:172879281-172879331	BJ	skin:	n/a
27	chr1:172864347-172864397	GM06990	blood:	n/a
28	chr1:172879281-172879331	HAEpiC	amniotic membrane:	n/a
29	chr1:172863499-172863549	SKMC	muscle:	n/a
30	chr1:172863499-172863549	HNPCEpiC	eye:	n/a
31	chr1:172852813-172852863	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:172879281-172879331	HCM	heart:	n/a
33	chr1:172863499-172863549	HCM	heart:	n/a
34	chr1:172852813-172852863	SAEC	small airway:	n/a
35	chr1:172879281-172879331	NB4	blood:	n/a
36	chr1:172863499-172863549	HUVEC	blood vessel:	n/a
37	chr1:172863499-172863549	HCT-116	colon:	n/a
38	chr1:172863499-172863549	CMK	blood:	n/a
39	chr1:172852813-172852863	GM12892	blood:	n/a
40	chr1:172863499-172863549	AG09309	skin:	n/a
41	chr1:172864347-172864397	HCT-116	colon:	n/a
42	chr1:172852813-172852863	NHDF-neo	bronchial:	n/a
43	chr1:172863499-172863549	PFSK-1	brain:	n/a
44	chr1:172852813-172852863	MCF10A-Er-Src	breast:	n/a
45	chr1:172852813-172852863	Caco-2	colon:	n/a
46	chr1:172864347-172864397	HUVEC	blood vessel:	n/a
47	chr1:172863499-172863549	SK-N-MC	brain:	n/a
48	chr1:172863499-172863549	RPTEC	kidney:	n/a
49	chr1:172852813-172852863	PANC-1	pancreas:	n/a
50	chr1:172863499-172863549	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:172864444..172866529-chr1:172867768..172870761,3	K562	blood:
2	chr1:172882184..172884117-chr1:172901661..172903834,2	MCF-7	breast:
3	chr1:172859088..172861490-chr1:172863508..172865755,2	K562	blood:
4	chr1:172855842..172858682-chr1:172958652..172961353,2	K562	blood:
5	chr1:172861260..172863626-chr1:172948311..172950341,2	K562	blood:
6	chr1:172864444..172866529-chr1:172867768..172870761,3	K562	blood:
7	chr1:172859088..172861490-chr1:172863508..172865755,2	K562	blood:
8	chr1:172854625..172857062-chr1:172865211..172867217,2	K562	blood:
9	chr1:172852617..172854204-chr1:172854324..172855885,2	MCF-7	breast:
10	chr1:172833934..172836062-chr1:172836107..172838430,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FASLG-1	chr1:172876040-172876392	ENSG00000224000
2	lnc-FASLG-1	chr1:172876520-172876824	ENSG00000224000
3	lnc-TNFSF18-3	chr1:172855087-172855398	NONHSAT007620
4	lnc-TNFSF18-2	chr1:172867285-172868044	NONHSAT007621

No data

Variant related genes	Relation type
ENSG00000224000	TF binding region
AIMP1P2	TF binding region
ENSG00000224000	CpG island
AIMP1P2	CpG island
ENSG00000227177	chromatin interactions

Extended variants
information (count: 1461 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1461 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115615011	chr1:172836950-172836951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367556709	chr1:172837014-172837015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546945438	chr1:172837053-172837054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149061909	chr1:172837117-172837118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544079633	chr1:172837148-172837149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78863889	chr1:172837162-172837163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372831215	chr1:172837189-172837190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184463660	chr1:172837219-172837220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561207434	chr1:172837272-172837273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569513938	chr1:172837331-172837332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539901799	chr1:172837383-172837384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74125986	chr1:172837397-172837398	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs186885488	chr1:172837420-172837421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566844583	chr1:172837464-172837465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534168256	chr1:172837473-172837474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191776606	chr1:172837496-172837497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573874953	chr1:172837549-172837550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111390071	chr1:172837570-172837571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537789866	chr1:172837598-172837599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114081822	chr1:172837612-172837613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143062578	chr1:172837633-172837634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377186701	chr1:172837674-172837675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138539035	chr1:172837742-172837743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546906009	chr1:172837756-172837757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116736367	chr1:172837768-172837769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566108704	chr1:172837769-172837770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114033528	chr1:172837784-172837785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571846668	chr1:172837813-172837814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551769517	chr1:172837855-172837856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542587118	chr1:172837857-172837858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571795984	chr1:172837873-172837874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534268557	chr1:172837912-172837913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534588368	chr1:172837939-172837940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532024842	chr1:172837975-172837976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140250596	chr1:172837976-172837977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201669142	chr1:172838021-172838022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189495411	chr1:172838064-172838065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563025731	chr1:172838078-172838079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181054837	chr1:172838080-172838081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552037716	chr1:172838162-172838163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566948479	chr1:172838187-172838188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145227759	chr1:172838201-172838202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376475674	chr1:172838202-172838203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549348076	chr1:172838215-172838216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567560249	chr1:172838312-172838313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538095587	chr1:172838368-172838369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556058244	chr1:172838402-172838403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34150039	chr1:172838407-172838408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548050267	chr1:172838457-172838458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185598795	chr1:172838468-172838469	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
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
Glioblastoma multiforme	21080181	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
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
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172820600-172840200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:172828600-172840600	Weak transcription	A549	lung
3	chr1:172828800-172840200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:172831200-172844000	Weak transcription	HUVEC	blood vessel
5	chr1:172836000-172837600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:172836000-172837600	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr1:172836400-172837000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:172836400-172837000	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr1:172836400-172837000	Enhancers	Dnd41	blood
10	chr1:172836400-172837400	Enhancers	Primary T cells from cord blood	blood
11	chr1:172836400-172837400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr1:172836600-172837200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:172836800-172837200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr1:172837000-172840200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:172837000-172844000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:172837200-172837400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr1:172837200-172837400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:172837200-172837600	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr1:172837400-172844000	Weak transcription	Primary T cells from cord blood	blood
20	chr1:172837400-172844000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:172837400-172844000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:172837400-172844000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:172837600-172839400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:172837600-172839400	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:172837600-172844200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr1:172839400-172840800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr1:172839400-172840800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr1:172840000-172840800	Enhancers	GM12878-XiMat	blood
29	chr1:172840200-172840600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:172840200-172840600	Enhancers	Hela-S3	cervix
31	chr1:172840200-172840800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:172840200-172840800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:172840200-172840800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:172840200-172840800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:172840200-172840800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:172840200-172840800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:172840200-172840800	Enhancers	Stomach Mucosa	stomach
38	chr1:172840200-172840800	Enhancers	HMEC	breast
39	chr1:172840200-172840800	Enhancers	NHEK	skin
40	chr1:172840400-172840800	Enhancers	Placenta Amnion	Placenta Amnion
41	chr1:172840600-172840800	Enhancers	A549	lung
42	chr1:172840600-172855200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:172840800-172843800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:172840800-172843800	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr1:172840800-172844000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:172840800-172844000	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr1:172840800-172844000	Weak transcription	NHEK	skin
48	chr1:172840800-172844200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:172843000-172843400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:172843800-172844600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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