Variant report

Variant	nsv598937
Chromosome Location	chr5:91275313-91381882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:91375827-91375830	GM12878	blood:	n/a	n/a
2	CBX3	chr5:91313395-91314027	HCT-116	colon:	n/a	n/a
3	CBX3	chr5:91315122-91315650	HCT-116	colon:	n/a	n/a
4	CEBPB	chr5:91280927-91281141	HepG2	liver:	n/a	chr5:91281056-91281067
5	CEBPB	chr5:91298908-91299168	HepG2	liver:	n/a	chr5:91299044-91299056
6	CEBPB	chr5:91281741-91282081	HepG2	liver:	n/a	chr5:91281924-91281935 chr5:91281925-91281936
7	CEBPB	chr5:91315118-91315514	Hela-S3	cervix:	n/a	chr5:91315210-91315221 chr5:91315210-91315223
8	CEBPB	chr5:91366092-91366382	HepG2	liver:	n/a	chr5:91366257-91366268 chr5:91366316-91366327
9	CEBPB	chr5:91375748-91376042	A549	lung:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
10	CEBPB	chr5:91313622-91314038	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:91297589-91297834	HepG2	liver:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
12	CEBPB	chr5:91297546-91297863	IMR90	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
13	CEBPB	chr5:91375704-91376012	HepG2	liver:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
14	CEBPB	chr5:91366107-91366340	A549	lung:	n/a	chr5:91366257-91366268 chr5:91366316-91366327
15	CEBPB	chr5:91296321-91296513	HepG2	liver:	n/a	chr5:91296386-91296397
16	CEBPB	chr5:91298859-91299124	IMR90	lung:	n/a	chr5:91299044-91299056
17	CEBPB	chr5:91297576-91297842	A549	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
18	CEBPB	chr5:91297518-91297861	Hela-S3	cervix:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
19	CEBPB	chr5:91327553-91327814	A549	lung:	n/a	n/a
20	CTCF	chr5:91346933-91346970	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:91346689-91347000	GM12878	blood:	n/a	n/a
22	CTCF	chr5:91346840-91346990	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr5:91346880-91347030	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:91346980-91347130	BE2_C	brain:	n/a	n/a
25	CTCF	chr5:91346776-91346858	GM19238	blood:	n/a	n/a
26	CTCF	chr5:91346620-91346770	GM12867	blood:	n/a	n/a
27	CTCF	chr5:91290803-91290856	GM10248	blood:	n/a	n/a
28	CTCF	chr5:91346766-91346824	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:91346880-91347030	HMF	breast:	n/a	n/a
30	CTCF	chr5:91346774-91346831	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:91346660-91346810	GM12872	blood:	n/a	n/a
32	CTCF	chr5:91346740-91346890	GM12874	blood:	n/a	n/a
33	CTCF	chr5:91346700-91346850	GM12867	blood:	n/a	n/a
34	CTCF	chr5:91378200-91378350	BE2_C	brain:	n/a	n/a
35	CTCF	chr5:91346776-91346993	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr5:91346916-91347001	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:91346780-91346930	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr5:91310973-91311038	GM20000	blood:	n/a	n/a
39	CTCF	chr5:91346762-91346863	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:91346920-91347070	GM12873	blood:	n/a	n/a
41	CTCF	chr5:91359213-91359274	GM10266	blood:	n/a	n/a
42	CTCF	chr5:91346700-91346850	GM12873	blood:	n/a	n/a
43	CTCF	chr5:91346771-91346806	GM19240	blood:	n/a	n/a
44	CTCF	chr5:91346760-91346910	A549	lung:	n/a	n/a
45	E2F4	chr5:91283630-91283713	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr5:91315292-91315636	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr5:91344273-91344473	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr5:91295681-91295870	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:91301746-91302182	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr5:91325284-91325472	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91303031-91303081	AG10803	skin:	n/a
2	chr5:91303031-91303081	BJ	skin:	n/a
3	chr5:91303031-91303081	HL-60	blood:	n/a
4	chr5:91298666-91298716	GM06990	blood:	n/a
5	chr5:91298666-91298716	ProgFib	skin:	n/a
6	chr5:91298666-91298716	T-47D	breast:	n/a
7	chr5:91303031-91303081	HCM	heart:	n/a
8	chr5:91298666-91298716	NHBE	bronchial:	n/a
9	chr5:91303031-91303081	HNPCEpiC	eye:	n/a
10	chr5:91298666-91298716	GM12878	blood:	n/a
11	chr5:91298666-91298716	LNCaP	prostate:	n/a
12	chr5:91298666-91298716	HCT-116	colon:	n/a
13	chr5:91303031-91303081	PFSK-1	brain:	n/a
14	chr5:91298666-91298716	Hela-S3	cervix:	n/a
15	chr5:91303031-91303081	AG04449	skin:	fetal
16	chr5:91303031-91303081	GM06990	blood:	n/a
17	chr5:91298666-91298716	MCF10A-Er-Src	breast:	n/a
18	chr5:91298666-91298716	GM12891	blood:	n/a
19	chr5:91298666-91298716	PFSK-1	brain:	n/a
20	chr5:91303031-91303081	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:91298666-91298716	HEK293	kidney:	embryo
22	chr5:91298666-91298716	CMK	blood:	n/a
23	chr5:91303031-91303081	PANC-1	pancreas:	n/a
24	chr5:91303031-91303081	BE2_C	brain:	n/a
25	chr5:91298666-91298716	HCM	heart:	n/a
26	chr5:91298666-91298716	A549	lung:	n/a
27	chr5:91303031-91303081	HCT-116	colon:	n/a
28	chr5:91298666-91298716	SK-N-MC	brain:	n/a
29	chr5:91303031-91303081	ProgFib	skin:	n/a
30	chr5:91303031-91303081	HRPEpiC	eye:	n/a
31	chr5:91303031-91303081	Hela-S3	cervix:	n/a
32	chr5:91303031-91303081	NHBE	bronchial:	n/a
33	chr5:91303031-91303081	NB4	blood:	n/a
34	chr5:91303031-91303081	HCPEpiC	choroid plexus:	n/a
35	chr5:91298666-91298716	Caco-2	colon:	n/a
36	chr5:91298666-91298716	K562	blood:	n/a
37	chr5:91298666-91298716	NT2-D1	testis:	n/a
38	chr5:91298666-91298716	H1-hESC	embryonic stem cell:	embryo
39	chr5:91303031-91303081	SK-N-SH	brain:	n/a
40	chr5:91303031-91303081	MCF10A-Er-Src	breast:	n/a
41	chr5:91303031-91303081	A549	lung:	n/a
42	chr5:91298666-91298716	ECC-1	luminal epithelium:	n/a
43	chr5:91298666-91298716	HL-60	blood:	n/a
44	chr5:91298666-91298716	U87	brain:	n/a
45	chr5:91298666-91298716	ovcar-3	ovarian:	n/a
46	chr5:91298666-91298716	NB4	blood:	n/a
47	chr5:91298666-91298716	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:91298666-91298716	AG04449	skin:	fetal
49	chr5:91298666-91298716	HIPEpiC	eye:	n/a
50	chr5:91298666-91298716	SK-N-SH_RA	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:90141991..90142609-chr5:91326921..91327421,2	MCF-7	breast:
2	chr11:118661976..118663890-chr5:91336617..91338563,2	MCF-7	breast:
3	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
4	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
5	chr20:13765598..13766099-chr5:91346247..91346777,2	MCF-7	breast:
6	chr5:91315876..91316579-chr6:144774937..144775884,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR98-5	chr5:91378414-91378637	XLOC_004470

No data

Variant related genes	Relation type
ENSG00000250049	TF binding region
ENSG00000250049	CpG island
ENSG00000164199	chromatin interactions
ENSG00000101247	chromatin interactions

Extended variants
information (count: 1082 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs421379	chr5:91275313-91275314	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs578062724	chr5:91275328-91275329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73771616	chr5:91275368-91275369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144940015	chr5:91275380-91275381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543527352	chr5:91275428-91275429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs16870311	chr5:91275431-91275432	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574071395	chr5:91275487-91275488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs80116478	chr5:91275496-91275497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373587910	chr5:91275520-91275521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140537889	chr5:91275525-91275526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543389559	chr5:91275534-91275535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528707040	chr5:91275596-91275597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560091264	chr5:91275599-91275600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548363704	chr5:91275665-91275666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528739459	chr5:91275711-91275712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568493710	chr5:91275743-91275744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367652137	chr5:91275867-91275868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144433194	chr5:91275899-91275900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189974011	chr5:91275916-91275917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183965412	chr5:91275918-91275919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538947411	chr5:91275960-91275961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558846484	chr5:91276006-91276007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188961171	chr5:91276025-91276026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565978172	chr5:91276074-91276075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534856182	chr5:91276115-91276116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554726097	chr5:91276130-91276131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574467731	chr5:91276162-91276163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111995744	chr5:91276185-91276186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371785486	chr5:91276192-91276193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs193087733	chr5:91276202-91276203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572897705	chr5:91276237-91276238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556689824	chr5:91276241-91276242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147814628	chr5:91276341-91276342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551967279	chr5:91276358-91276359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77161145	chr5:91276435-91276436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559659059	chr5:91276443-91276444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565310381	chr5:91276467-91276468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528743702	chr5:91276496-91276497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542047413	chr5:91276507-91276508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530661527	chr5:91276527-91276528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562281437	chr5:91276539-91276540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141445772	chr5:91276545-91276546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551013565	chr5:91276553-91276554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570764349	chr5:91276554-91276555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533415366	chr5:91276567-91276568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34957407	chr5:91276585-91276586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368375552	chr5:91276591-91276592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371361400	chr5:91276593-91276594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144014093	chr5:91276703-91276704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566016213	chr5:91276720-91276721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91271800-91275600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr5:91273400-91276600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:91274200-91275600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:91274400-91275400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:91274600-91276200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:91274800-91280000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:91275200-91276200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr5:91275400-91275800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr5:91275600-91276000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:91275600-91279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr5:91275800-91276800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:91276000-91276800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:91276200-91276600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:91276200-91277200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:91276600-91280000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:91276600-91280000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr5:91276800-91279800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr5:91276800-91280200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr5:91277200-91279800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:91279800-91280600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:91279800-91280600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:91279800-91280600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:91280000-91280400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:91280000-91280600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:91280000-91281200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:91280000-91281600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:91280200-91280400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:91280400-91280600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr5:91280400-91280800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr5:91280600-91280800	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr5:91280600-91281000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:91280600-91281600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:91280600-91281800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:91280800-91281200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:91280800-91281800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr5:91281000-91281400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:91281600-91281800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:91281600-91282000	Enhancers	Fetal Lung	lung
39	chr5:91281800-91282000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:91282000-91282200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:91282000-91282400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:91282400-91282800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:91294400-91295200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr5:91295200-91302800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr5:91298200-91298600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:91298200-91298800	Enhancers	NHLF	lung
47	chr5:91298600-91299200	Enhancers	Fetal Lung	lung
48	chr5:91298600-91299600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:91299200-91299600	Weak transcription	Fetal Lung	lung
50	chr5:91299600-91300000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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