Variant report

Variant	nsv538392
Chromosome Location	chr6:101938381-102148360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:367)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:102056602-102056963	HepG2	liver:	n/a	n/a
2	BACH1	chr6:102045581-102045848	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:101965496-101965827	GM12878	blood:	n/a	chr6:101965664-101965674 chr6:101965663-101965674
4	BATF	chr6:101965476-101965853	GM12878	blood:	n/a	chr6:101965664-101965674 chr6:101965663-101965674
5	BATF	chr6:102053779-102054143	GM12878	blood:	n/a	n/a
6	BATF	chr6:102053735-102054095	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:102062798-102062989	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr6:102053790-102054092	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:101965565-101965767	GM12878	blood:	n/a	chr6:101965676-101965685
10	BCL11A	chr6:102053843-102054122	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:102126920-102126952	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:102099482-102099484	GM12878	blood:	n/a	n/a
13	CBX3	chr6:102062519-102063174	HCT-116	colon:	n/a	chr6:102063060-102063071
14	CBX3	chr6:102062577-102063026	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:102053768-102054276	HCT-116	colon:	n/a	n/a
16	CCNT2	chr6:102021902-102022045	K562	blood:	n/a	n/a
17	CEBPB	chr6:102045561-102046041	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:102062640-102063157	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:102037085-102037425	HepG2	liver:	n/a	chr6:102037246-102037257
20	CEBPB	chr6:102086759-102087085	ECC-1	luminal epithelium:	n/a	chr6:102086970-102086981
21	CEBPB	chr6:101949315-101949469	A549	lung:	n/a	chr6:101949332-101949345 chr6:101949332-101949345 chr6:101949424-101949432
22	CEBPB	chr6:102062489-102063215	HCT-116	colon:	n/a	n/a
23	CEBPB	chr6:102037117-102037423	A549	lung:	n/a	chr6:102037246-102037257
24	CEBPB	chr6:101993455-101993816	IMR90	lung:	n/a	chr6:101993619-101993630 chr6:101993621-101993630 chr6:101993621-101993632 chr6:101993619-101993632
25	CEBPB	chr6:102086871-102087014	HepG2	liver:	n/a	chr6:102086970-102086981
26	CEBPB	chr6:102037169-102037369	K562	blood:	n/a	chr6:102037246-102037257
27	CEBPB	chr6:102086791-102087116	H1-hESC	embryonic stem cell:	n/a	chr6:102086970-102086981
28	CEBPB	chr6:102086613-102087169	MCF-7	breast:	n/a	chr6:102086970-102086981
29	CEBPB	chr6:102086435-102087130	IMR90	lung:	n/a	chr6:102086970-102086981
30	CEBPB	chr6:102032609-102032875	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:102062818-102063063	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:101993488-101993761	HepG2	liver:	n/a	chr6:101993619-101993630 chr6:101993621-101993630 chr6:101993621-101993632 chr6:101993619-101993632
33	CEBPB	chr6:102037097-102037430	IMR90	lung:	n/a	chr6:102037246-102037257
34	CEBPB	chr6:101985779-101986252	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:102056590-102056959	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:102086410-102087126	HepG2	liver:	n/a	chr6:102086970-102086981
37	CEBPB	chr6:101946166-101946269	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:101985994-101986190	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:102005546-102005865	HepG2	liver:	n/a	chr6:102005803-102005811 chr6:102005707-102005716 chr6:102005707-102005718
40	CEBPB	chr6:101982244-101982591	IMR90	lung:	n/a	chr6:101982414-101982426
41	CEBPB	chr6:102037169-102037304	HepG2	liver:	n/a	chr6:102037246-102037257
42	CEBPB	chr6:102086438-102087046	A549	lung:	n/a	chr6:102086970-102086981
43	CEBPB	chr6:102086800-102087161	ECC-1	luminal epithelium:	n/a	chr6:102086970-102086981
44	CEBPB	chr6:102032600-102032930	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr6:102075394-102075424	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:101955642-101955722	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr6:102062656-102062971	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr6:102062494-102063104	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr6:102094080-102094230	HMF	breast:	n/a	n/a
50	CTCF	chr6:102084751-102084814	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102115051-102115101	GM12891	blood:	n/a
2	chr6:102115051-102115101	GM12891	blood:	n/a
3	chr6:101993140-101993190	SK-N-SH_RA	brain:	n/a
4	chr6:102098727-102098777	LNCaP	prostate:	n/a
5	chr6:102062733-102062783	NT2-D1	testis:	n/a
6	chr6:102055059-102055109	HUVEC	blood vessel:	n/a
7	chr6:102088363-102088413	HEEpiC	esophagus:	n/a
8	chr6:102098727-102098777	HEEpiC	esophagus:	n/a
9	chr6:101993140-101993190	HMEC	breast:	n/a
10	chr6:101993140-101993190	HepG2	liver:	n/a
11	chr6:102115051-102115101	GM12878	blood:	n/a
12	chr6:101993140-101993190	LNCaP	prostate:	n/a
13	chr6:102098727-102098777	HUVEC	blood vessel:	n/a
14	chr6:101993140-101993190	HNPCEpiC	eye:	n/a
15	chr6:102098727-102098777	AG09309	skin:	n/a
16	chr6:102062733-102062783	HUVEC	blood vessel:	n/a
17	chr6:102062733-102062783	SKMC	muscle:	n/a
18	chr6:102055059-102055109	HCM	heart:	n/a
19	chr6:102115051-102115101	HAEpiC	amniotic membrane:	n/a
20	chr6:102098727-102098777	AG04450	lung:	fetal
21	chr6:102055059-102055109	U87	brain:	n/a
22	chr6:101993140-101993190	NHBE	bronchial:	n/a
23	chr6:102098727-102098777	AoSMC	blood vessel:	n/a
24	chr6:102062733-102062783	IMR90	lung:	fetal
25	chr6:101993140-101993190	CMK	blood:	n/a
26	chr6:102088363-102088413	AG04450	lung:	fetal
27	chr6:102115051-102115101	GM19239	blood:	n/a
28	chr6:102115051-102115101	AG09309	skin:	n/a
29	chr6:102088363-102088413	SK-N-SH_RA	brain:	n/a
30	chr6:102062733-102062783	Jurkat	blood:	n/a
31	chr6:102098727-102098777	GM12891	blood:	n/a
32	chr6:102062733-102062783	AG09309	skin:	n/a
33	chr6:102115051-102115101	HUVEC	blood vessel:	n/a
34	chr6:102088363-102088413	HRCEpiC	kidney:	n/a
35	chr6:102055059-102055109	AG10803	skin:	n/a
36	chr6:101993140-101993190	AG10803	skin:	n/a
37	chr6:101993140-101993190	MCF10A-Er-Src	breast:	n/a
38	chr6:102055059-102055109	NHBE	bronchial:	n/a
39	chr6:102115051-102115101	HRPEpiC	eye:	n/a
40	chr6:102062733-102062783	ECC-1	luminal epithelium:	n/a
41	chr6:101993140-101993190	Caco-2	colon:	n/a
42	chr6:102088363-102088413	HRPEpiC	eye:	n/a
43	chr6:102088363-102088413	GM12891	blood:	n/a
44	chr6:102062733-102062783	BE2_C	brain:	n/a
45	chr6:102115051-102115101	SAEC	small airway:	n/a
46	chr6:102088363-102088413	SKMC	muscle:	n/a
47	chr6:102115051-102115101	RPTEC	kidney:	n/a
48	chr6:102055059-102055109	AoSMC	blood vessel:	n/a
49	chr6:102062733-102062783	SK-N-SH	brain:	n/a
50	chr6:101993140-101993190	MCF-7	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:102000178..102002016-chr6:102006713..102008443,2	K562	blood:
2	chr6:101845030..101845934-chr6:102093542..102094670,3	MCF-7	breast:
3	chr6:102014386..102015979-chr6:102018892..102021029,2	K562	blood:
4	chr6:102028266..102030004-chr6:102035666..102038044,2	K562	blood:
5	chr6:102014386..102015979-chr6:102018892..102021029,2	K562	blood:
6	chr6:102028266..102030004-chr6:102035666..102038044,2	K562	blood:
7	chr6:101950752..101952514-chr6:101954590..101957331,2	K562	blood:
8	chr6:101957360..101958960-chr6:101959179..101961088,2	K562	blood:
9	chr6:101950752..101952514-chr6:101954590..101957331,2	K562	blood:
10	chr6:101971431..101973634-chr6:101982857..101985003,2	MCF-7	breast:
11	chr6:102000178..102002016-chr6:102006713..102008443,2	K562	blood:
12	chr6:102066602..102069152-chr6:102074799..102076999,2	MCF-7	breast:
13	chr6:101957360..101958960-chr6:101959179..101961088,2	K562	blood:
14	chr6:101934940..101937511-chr6:101959747..101962607,2	K562	blood:
15	chr3:61667747..61668495-chr6:102049744..102050312,2	MCF-7	breast:
16	chr6:101971431..101973634-chr6:101982857..101985003,2	MCF-7	breast:

No data

Variant related genes	Relation type
GRIK2	TF binding region
GRIK2	CpG island
ENSG00000164418	chromatin interactions

Extended variants
information (count: 4859 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4859 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555524986	chr6:101950610-101950611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76960677	chr6:101950611-101950612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554670113	chr6:101950650-101950651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35386200	chr6:101950690-101950691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142135238	chr6:101950694-101950695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373392118	chr6:101950704-101950705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540375256	chr6:101950716-101950717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150136115	chr6:101950747-101950748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577059413	chr6:101950819-101950820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541286694	chr6:101950841-101950842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138663034	chr6:101950846-101950847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563679517	chr6:101950853-101950854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530788787	chr6:101950861-101950862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542729707	chr6:101950871-101950872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148902154	chr6:101950884-101950885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528666881	chr6:101950939-101950940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143466677	chr6:101950970-101950971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs137859689	chr6:101950971-101950972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532818394	chr6:101950975-101950976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550962994	chr6:101951055-101951056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568885119	chr6:101951086-101951087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190322754	chr6:101951152-101951153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182496274	chr6:101951190-101951191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548290693	chr6:101951193-101951194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533788827	chr6:101951202-101951203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558702264	chr6:101951203-101951204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367815113	chr6:101951205-101951206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74828688	chr6:101951246-101951247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186740526	chr6:101951299-101951300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80350887	chr6:101951336-101951337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192041245	chr6:101951362-101951363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575248916	chr6:101951403-101951404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373796043	chr6:101951432-101951433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376680371	chr6:101951441-101951442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561096124	chr6:101951486-101951487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2224201	chr6:101951502-101951503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs528322080	chr6:101951507-101951508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540496176	chr6:101951600-101951601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34764416	chr6:101951634-101951635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541078023	chr6:101951690-101951691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563316993	chr6:101951720-101951721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565494648	chr6:101951725-101951726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532560754	chr6:101951735-101951736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529190364	chr6:101951755-101951756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145960223	chr6:101951768-101951769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549328142	chr6:101951771-101951772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72957121	chr6:101951786-101951787	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs78470034	chr6:101951793-101951794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548198975	chr6:101951881-101951882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566606815	chr6:101951890-101951891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101950600-101951200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr6:101950600-101951200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr6:101950800-101951200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:101951200-101951600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:101951600-101951800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:101951800-101965000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:101956000-101956400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:101957200-101957600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:101961200-101961400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:101961400-101962000	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr6:101963400-101964400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr6:101963800-101964600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:101965000-101965400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:101967000-101967400	Enhancers	Fetal Brain Male	brain
15	chr6:101970200-101970600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:101978600-101978800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:101978800-101979600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:101978800-101982600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:101979600-101979800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:101979800-101980000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:101980000-101983800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:101981400-101981800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:101981800-101982400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr6:101981800-101982600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:101982000-101982400	Enhancers	NH-A	brain
26	chr6:101982000-101982800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:101982000-101983000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr6:101982400-101982600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr6:101982400-101982800	Weak transcription	NH-A	brain
30	chr6:101982600-101983000	Active TSS	Osteobl	bone
31	chr6:101982600-101983200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:101982600-101983200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:101982600-101983200	Active TSS	Ovary	ovary
34	chr6:101982600-101983800	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr6:101982800-101983000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:101982800-101983000	Enhancers	NH-A	brain
37	chr6:101982800-101983400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:101983000-101983200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr6:101983000-101983400	Active TSS	Fetal Lung	lung
40	chr6:101983000-101986000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr6:101983000-101987200	Weak transcription	NH-A	brain
42	chr6:101983200-101983400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:101983200-101985800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:101983200-101991400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:101983400-101985200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:101983400-101987400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:101983800-101984200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:101983800-101984200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:101984200-101985600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr6:101985200-101985600	Enhancers	Fetal Brain Male	brain

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