Variant report

Variant	nsv549194
Chromosome Location	chr1:216055853-216072598
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	CEBPB	chr1:216060514-216060741	HepG2	liver:	n/a	chr1:216060625-216060636
2	CEBPB	chr1:216065111-216065415	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:216060490-216060784	IMR90	lung:	n/a	chr1:216060625-216060636
4	CTCF	chr1:216061560-216061710	SAEC	small airway:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
5	CTCF	chr1:216061628-216061703	SK-N-SH_RA	brain:	n/a	chr1:216061681-216061699
6	CTCF	chr1:216061566-216061759	HepG2	liver:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
7	CTCF	chr1:216061623-216061747	LNCaP	prostate:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
8	CTCF	chr1:216061632-216061724	GM10248	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
9	CTCF	chr1:216061592-216061853	HCT-116	colon:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
10	CTCF	chr1:216065141-216065177	Gliobla	brain:	n/a	n/a
11	CTCF	chr1:216061549-216061853	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
12	CTCF	chr1:216061660-216061710	GM10266	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
13	CTCF	chr1:216061580-216061730	A549	lung:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
14	CTCF	chr1:216061640-216061790	NHEK	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
15	CTCF	chr1:216061618-216061751	Hela-S3	cervix:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
16	CTCF	chr1:216061620-216061770	BE2_C	brain:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
17	CTCF	chr1:216065178-216065185	Gliobla	brain:	n/a	n/a
18	CTCF	chr1:216061623-216061847	Fibrobl	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
19	CTCF	chr1:216061640-216061790	WERI-Rb-1	eye:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
20	CTCF	chr1:216061630-216061743	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
21	CTCF	chr1:216061600-216061750	GM12865	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
22	CTCF	chr1:216061580-216061730	NB4	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
23	CTCF	chr1:216061610-216061758	K562	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
24	CTCF	chr1:216061540-216061690	AG09319	gingival:	n/a	n/a
25	CTCF	chr1:216061620-216061770	GM12878	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
26	CTCF	chr1:216061589-216061796	SK-N-SH_RA	brain:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
27	CTCF	chr1:216061640-216061790	HMF	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
28	CTCF	chr1:216065100-216065250	AG09319	gingival:	n/a	n/a
29	CTCF	chr1:216064960-216065110	HMF	breast:	n/a	n/a
30	CTCF	chr1:216061820-216061970	HMEC	breast:	n/a	n/a
31	CTCF	chr1:216061680-216061830	AG09309	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
32	CTCF	chr1:216061743-216061821	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:216061420-216061570	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr1:216061600-216061750	GM12864	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
35	CTCF	chr1:216061540-216061690	GM12869	blood:	n/a	n/a
36	CTCF	chr1:216061711-216061717	GM10266	blood:	n/a	n/a
37	CTCF	chr1:216061571-216061868	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
38	CTCF	chr1:216061420-216061570	GM12865	blood:	n/a	n/a
39	CTCF	chr1:216061600-216061750	HRPEpiC	eye:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
40	CTCF	chr1:216061600-216061750	HAc	cerebellar:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
41	CTCF	chr1:216058148-216058226	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:216061580-216061730	BE2_C	brain:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
43	CTCF	chr1:216061667-216061755	NHEK	skin:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
44	CTCF	chr1:216061580-216061730	WERI-Rb-1	eye:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
45	CTCF	chr1:216061598-216061779	GM12878	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
46	CTCF	chr1:216060880-216061030	HPF	lung:	n/a	chr1:216060989-216060996 chr1:216060977-216060998
47	CTCF	chr1:216061640-216061790	GM12866	blood:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
48	CTCF	chr1:216061540-216061690	GM12873	blood:	n/a	n/a
49	CTCF	chr1:216061600-216061750	MCF-7	breast:	n/a	chr1:216061683-216061704 chr1:216061681-216061699
50	CTCF	chr1:216061684-216061851	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:216058191-216058241	HCT-116	colon:	n/a
2	chr1:216058191-216058241	HRCEpiC	kidney:	n/a
3	chr1:216058191-216058241	HRE	kidney:	n/a
4	chr1:216058191-216058241	A549	lung:	n/a
5	chr1:216058191-216058241	ECC-1	luminal epithelium:	n/a
6	chr1:216058191-216058241	HNPCEpiC	eye:	n/a
7	chr1:216058191-216058241	AG09319	gingival:	n/a
8	chr1:216058191-216058241	IMR90	lung:	fetal
9	chr1:216058191-216058241	BJ	skin:	n/a
10	chr1:216058191-216058241	ProgFib	skin:	n/a
11	chr1:216058191-216058241	GM12892	blood:	n/a
12	chr1:216058191-216058241	NHBE	bronchial:	n/a
13	chr1:216058191-216058241	GM12878	blood:	n/a
14	chr1:216058191-216058241	CMK	blood:	n/a
15	chr1:216058191-216058241	SK-N-MC	brain:	n/a
16	chr1:216058191-216058241	HEK293	kidney:	embryo
17	chr1:216058191-216058241	GM06990	blood:	n/a
18	chr1:216058191-216058241	HCM	heart:	n/a
19	chr1:216058191-216058241	AG04449	skin:	fetal
20	chr1:216058191-216058241	Hela-S3	cervix:	n/a
21	chr1:216058191-216058241	SKMC	muscle:	n/a
22	chr1:216058191-216058241	SK-N-SH_RA	brain:	n/a
23	chr1:216058191-216058241	GM12891	blood:	n/a
24	chr1:216058191-216058241	PFSK-1	brain:	n/a
25	chr1:216058191-216058241	Hepatocyte	liver:	n/a
26	chr1:216058191-216058241	MCF-7	breast:	n/a
27	chr1:216058191-216058241	NH-A	brain:	n/a
28	chr1:216058191-216058241	HL-60	blood:	n/a
29	chr1:216058191-216058241	HCPEpiC	choroid plexus:	n/a
30	chr1:216058191-216058241	H1-hESC	embryonic stem cell:	embryo
31	chr1:216058191-216058241	T-47D	breast:	n/a
32	chr1:216058191-216058241	NT2-D1	testis:	n/a
33	chr1:216058191-216058241	PANC-1	pancreas:	n/a
34	chr1:216058191-216058241	MCF10A-Er-Src	breast:	n/a
35	chr1:216058191-216058241	BE2_C	brain:	n/a
36	chr1:216058191-216058241	HAEpiC	amniotic membrane:	n/a
37	chr1:216058191-216058241	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:216058191-216058241	LNCaP	prostate:	n/a
39	chr1:216058191-216058241	PrEC	prostate:	n/a
40	chr1:216058191-216058241	HIPEpiC	eye:	n/a
41	chr1:216058191-216058241	HEEpiC	esophagus:	n/a
42	chr1:216058191-216058241	AoSMC	blood vessel:	n/a
43	chr1:216058191-216058241	Jurkat	blood:	n/a
44	chr1:216058191-216058241	HMEC	breast:	n/a
45	chr1:216058191-216058241	SK-N-SH	brain:	n/a
46	chr1:216058191-216058241	NB4	blood:	n/a
47	chr1:216058191-216058241	AG04450	lung:	fetal
48	chr1:216058191-216058241	GM19239	blood:	n/a
49	chr1:216058191-216058241	NHDF-neo	bronchial:	n/a
50	chr1:216058191-216058241	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:216061653..216062167-chr1:216394272..216395211,2	MCF-7	breast:
2	chr1:216061208..216061956-chr1:216293049..216293584,2	MCF-7	breast:
3	chr1:215883862..215884424-chr1:216061346..216062151,2	MCF-7	breast:
4	chr1:216061603..216062225-chr1:216207802..216208490,2	MCF-7	breast:
5	chr1:216061210..216062115-chr1:216367528..216368046,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCTD3-1	chr1:216059924-216059983	ENSG00000229242.1

Variant related genes	Relation type
ENSG00000229242	TF binding region
ENSG00000229242	CpG island

Extended variants
information (count: 695 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17567651	chr1:216055853-216055854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534531438	chr1:216055860-216055861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146000632	chr1:216055874-216055875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138648651	chr1:216055894-216055895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547364969	chr1:216055919-216055920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542523478	chr1:216055983-216055984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539738404	chr1:216055993-216055994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57823793	chr1:216056048-216056049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570694497	chr1:216056060-216056061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1981229	chr1:216056071-216056072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140145656	chr1:216056147-216056148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200743116	chr1:216056148-216056149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560740454	chr1:216056181-216056182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537960233	chr1:216056203-216056204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1981228	chr1:216056210-216056211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113403262	chr1:216056217-216056218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540274753	chr1:216056287-216056288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34744699	chr1:216056318-216056319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553793221	chr1:216056345-216056346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17025548	chr1:216056348-216056349	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
21	rs150753629	chr1:216056378-216056379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562723114	chr1:216056379-216056380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34650128	chr1:216056417-216056418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576124242	chr1:216056460-216056461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6673555	chr1:216056499-216056500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561875237	chr1:216056519-216056520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77614860	chr1:216056532-216056533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547430330	chr1:216056557-216056558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561594168	chr1:216056602-216056603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188741861	chr1:216056634-216056635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6665181	chr1:216056638-216056639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550181697	chr1:216056649-216056650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570311462	chr1:216056710-216056711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535696534	chr1:216056714-216056715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549548493	chr1:216056715-216056716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377700833	chr1:216056739-216056740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192533540	chr1:216056755-216056756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577862084	chr1:216056773-216056774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1556940	chr1:216056779-216056780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553805485	chr1:216056781-216056782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184913943	chr1:216056783-216056784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564172477	chr1:216056811-216056812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539734933	chr1:216056843-216056844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556221173	chr1:216056848-216056849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576265449	chr1:216056885-216056886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73090771	chr1:216056972-216056973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561536818	chr1:216056973-216056974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546600425	chr1:216057005-216057006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572220214	chr1:216057010-216057011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189128767	chr1:216057054-216057055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
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
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216055400-216064200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:216059000-216059600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr1:216059600-216060800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:216060800-216061600	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr1:216060800-216062000	Enhancers	Liver	Liver
6	chr1:216061000-216061400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:216061000-216061400	Enhancers	Brain Germinal Matrix	brain
8	chr1:216061000-216061800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr1:216061400-216061600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:216061400-216064200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:216061600-216062800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:216061600-216065000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr1:216062800-216063800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:216063200-216063400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:216063200-216063800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:216063400-216064400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:216063600-216064200	Active TSS	GM12878-XiMat	blood
18	chr1:216063800-216064200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:216063800-216064800	Enhancers	Adipose Nuclei	Adipose
20	chr1:216063800-216065600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:216064200-216064400	Weak transcription	GM12878-XiMat	blood
22	chr1:216064200-216064800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:216064200-216064800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:216064200-216065600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:216064400-216064800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:216064400-216064800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:216064400-216064800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:216064400-216065000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr1:216064400-216065200	Enhancers	GM12878-XiMat	blood
30	chr1:216064400-216065400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:216064600-216064800	Enhancers	Fetal Kidney	kidney
32	chr1:216064600-216065000	Enhancers	Osteobl	bone
33	chr1:216064600-216065200	Enhancers	NHDF-Ad	bronchial
34	chr1:216064600-216065400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:216064600-216065600	Enhancers	NHLF	lung
36	chr1:216064800-216065000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:216064800-216067600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:216065000-216065200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:216065000-216065200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:216065000-216065200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:216065000-216065400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr1:216065000-216065400	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr1:216065200-216065400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:216065200-216065400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:216065200-216065400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr1:216065400-216065800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr1:216065400-216068800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr1:216065600-216066200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:216067600-216069400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:216067800-216068600	Enhancers	Primary hematopoietic stem cells	blood

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