Variant report

Variant	nsv481970
Chromosome Location	chr6:161961940-162207434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1408)
CpG islands
(count:734)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:162005585-162005674	K562	blood:	n/a	n/a
2	ATF1	chr6:162131444-162131661	K562	blood:	n/a	n/a
3	ATF1	chr6:162132283-162132287	K562	blood:	n/a	n/a
4	ATF1	chr6:162140696-162140749	K562	blood:	n/a	n/a
5	ATF1	chr6:162004714-162004819	K562	blood:	n/a	n/a
6	ATF1	chr6:161971326-161971631	K562	blood:	n/a	n/a
7	ATF1	chr6:162206880-162206984	K562	blood:	n/a	n/a
8	ATF1	chr6:161999566-161999833	K562	blood:	n/a	n/a
9	ATF2	chr6:161964957-161965386	GM12878	blood:	n/a	n/a
10	ATF3	chr6:161971276-161971680	K562	blood:	n/a	n/a
11	ATF3	chr6:162040045-162040462	K562	blood:	n/a	n/a
12	BACH1	chr6:162053102-162053295	H1-hESC	embryonic stem cell:	n/a	chr6:162053163-162053177
13	BACH1	chr6:162051173-162051178	K562	blood:	n/a	n/a
14	BACH1	chr6:162062267-162062596	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:162104075-162104373	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr6:162161546-162161747	GM12878	blood:	n/a	n/a
17	BATF	chr6:161965025-161965281	GM12878	blood:	n/a	chr6:161965148-161965158 chr6:161965147-161965158
18	BATF	chr6:161965002-161965288	GM12878	blood:	n/a	chr6:161965148-161965158 chr6:161965147-161965158
19	BCL11A	chr6:162148231-162148386	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr6:162184127-162184365	GM12878	blood:	n/a	n/a
21	BCL3	chr6:162184122-162184349	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:162164901-162165154	GM12878	blood:	n/a	n/a
23	CEBPB	chr6:162193250-162193574	HepG2	liver:	n/a	chr6:162193399-162193410
24	CEBPB	chr6:161971360-161971635	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:162040141-162040465	IMR90	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
26	CEBPB	chr6:161971361-161971639	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:162040128-162040496	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
28	CEBPB	chr6:162157986-162158258	A549	lung:	n/a	chr6:162158110-162158121
29	CEBPB	chr6:162073871-162074166	A549	lung:	n/a	n/a
30	CEBPB	chr6:162040153-162040413	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
31	CEBPB	chr6:162172357-162172763	A549	lung:	n/a	chr6:162172578-162172587 chr6:162172578-162172589
32	CEBPB	chr6:162086304-162086601	K562	blood:	n/a	chr6:162086444-162086457 chr6:162086444-162086455
33	CEBPB	chr6:162004658-162004765	H1-hESC	embryonic stem cell:	n/a	chr6:162004733-162004744
34	CEBPB	chr6:162004427-162005114	HCT-116	colon:	n/a	chr6:162004733-162004744
35	CEBPB	chr6:162172451-162172736	HepG2	liver:	n/a	chr6:162172578-162172587 chr6:162172578-162172589
36	CEBPB	chr6:162039972-162040478	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
37	CEBPB	chr6:161971326-161971679	A549	lung:	n/a	n/a
38	CEBPB	chr6:162169905-162170028	K562	blood:	n/a	n/a
39	CEBPB	chr6:161971294-161971642	K562	blood:	n/a	n/a
40	CEBPB	chr6:162004564-162004904	A549	lung:	n/a	chr6:162004733-162004744
41	CEBPB	chr6:162193296-162193557	Hela-S3	cervix:	n/a	chr6:162193399-162193410
42	CEBPB	chr6:162040075-162040483	HepG2	liver:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
43	CEBPB	chr6:162070447-162070488	A549	lung:	n/a	n/a
44	CEBPB	chr6:162039967-162040513	MCF-7	breast:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
45	CEBPB	chr6:162039960-162040482	MCF-7	breast:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
46	CEBPB	chr6:161997466-161997775	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:162040099-162040427	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
48	CEBPB	chr6:162040089-162040485	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
49	CEBPB	chr6:162004573-162004922	K562	blood:	n/a	chr6:162004733-162004744
50	CEBPB	chr6:162157995-162158268	HepG2	liver:	n/a	chr6:162158110-162158121

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162148153-162148203	AG09309	skin:	n/a
2	chr6:162148153-162148203	ProgFib	skin:	n/a
3	chr6:162148153-162148203	AG09309	skin:	n/a
4	chr6:162148153-162148203	ProgFib	skin:	n/a
5	chr6:162067177-162067227	PrEC	prostate:	n/a
6	chr6:161995369-161995419	Caco-2	colon:	n/a
7	chr6:161995337-161995387	CMK	blood:	n/a
8	chr6:162064339-162064389	SAEC	small airway:	n/a
9	chr6:162067177-162067227	RPTEC	kidney:	n/a
10	chr6:161995369-161995419	NB4	blood:	n/a
11	chr6:162068382-162068432	Hepatocyte	liver:	n/a
12	chr6:161995337-161995387	SAEC	small airway:	n/a
13	chr6:162066927-162066977	MCF10A-Er-Src	breast:	n/a
14	chr6:162064339-162064389	T-47D	breast:	n/a
15	chr6:162068382-162068432	HRE	kidney:	n/a
16	chr6:162066927-162066977	SK-N-SH_RA	brain:	n/a
17	chr6:161995302-161995352	HAEpiC	amniotic membrane:	n/a
18	chr6:161995369-161995419	NT2-D1	testis:	n/a
19	chr6:162060886-162060936	PANC-1	pancreas:	n/a
20	chr6:162067177-162067227	NH-A	brain:	n/a
21	chr6:162067688-162067738	PFSK-1	brain:	n/a
22	chr6:162068382-162068432	K562	blood:	n/a
23	chr6:162068382-162068432	SK-N-SH_RA	brain:	n/a
24	chr6:162067177-162067227	IMR90	lung:	fetal
25	chr6:162067177-162067227	Caco-2	colon:	n/a
26	chr6:162067688-162067738	HCT-116	colon:	n/a
27	chr6:162068382-162068432	HUVEC	blood vessel:	n/a
28	chr6:161995337-161995387	AG09309	skin:	n/a
29	chr6:162064339-162064389	GM12891	blood:	n/a
30	chr6:162066927-162066977	SK-N-SH	brain:	n/a
31	chr6:162067177-162067227	HEK293	kidney:	embryo
32	chr6:162066927-162066977	AG04449	skin:	fetal
33	chr6:162064339-162064389	K562	blood:	n/a
34	chr6:161995369-161995419	HRPEpiC	eye:	n/a
35	chr6:162148153-162148203	HRE	kidney:	n/a
36	chr6:162071140-162071190	MCF10A-Er-Src	breast:	n/a
37	chr6:162071140-162071190	GM19239	blood:	n/a
38	chr6:161995369-161995419	IMR90	lung:	fetal
39	chr6:162065571-162065621	Hela-S3	cervix:	n/a
40	chr6:162148153-162148203	Jurkat	blood:	n/a
41	chr6:162067177-162067227	HNPCEpiC	eye:	n/a
42	chr6:161995302-161995352	HEEpiC	esophagus:	n/a
43	chr6:162068382-162068432	SK-N-SH	brain:	n/a
44	chr6:162068382-162068432	GM19239	blood:	n/a
45	chr6:162065571-162065621	T-47D	breast:	n/a
46	chr6:162148153-162148203	K562	blood:	n/a
47	chr6:162067688-162067738	MCF-7	breast:	n/a
48	chr6:161995369-161995419	MCF10A-Er-Src	breast:	n/a
49	chr6:162067688-162067738	IMR90	lung:	fetal
50	chr6:161995337-161995387	Hela-S3	cervix:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:162135808..162138276-chr6:162142475..162145172,2	K562	blood:
2	chr6:162056640..162058918-chr6:162062226..162064429,2	K562	blood:
3	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
4	chr6:162111336..162114011-chr6:162137192..162139483,2	K562	blood:
5	chr6:161966825..161970007-chr6:161974073..161976606,3	K562	blood:
6	chr6:161965795..161968097-chr6:161969436..161971580,2	K562	blood:
7	chr6:161964543..161966481-chr6:161967748..161969351,2	K562	blood:
8	chr6:161964543..161966481-chr6:161967748..161969351,2	K562	blood:
9	chr6:162111336..162114011-chr6:162137192..162139483,2	K562	blood:
10	chr6:162039551..162040468-chr6:162115665..162116674,7	MCF-7	breast:
11	chr6:162022910..162024654-chr6:162024740..162027099,2	K562	blood:
12	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:
13	chr6:162001523..162004451-chr6:162007412..162009361,2	K562	blood:
14	chr6:162039551..162040468-chr6:162115665..162116674,7	MCF-7	breast:
15	chr6:162000857..162002528-chr6:162026039..162027693,2	K562	blood:
16	chr6:162000857..162002528-chr6:162026039..162027693,2	K562	blood:
17	chr6:162080897..162083173-chr6:162084992..162086582,2	K562	blood:
18	chr6:162064140..162064803-chr7:123198816..123199394,2	MCF-7	breast:
19	chr6:162115124..162116676-chr6:162119287..162121862,2	K562	blood:
20	chr6:162056640..162058918-chr6:162062226..162064429,2	K562	blood:
21	chr6:162135808..162138276-chr6:162142475..162145172,2	K562	blood:
22	chr20:46012429..46013123-chr6:162169752..162170322,2	MCF-7	breast:
23	chr6:162115124..162116676-chr6:162119287..162121862,2	K562	blood:
24	chr6:161962166..161963929-chr6:161965968..161968206,2	K562	blood:
25	chr6:161864849..161867369-chr6:162020785..162023410,2	K562	blood:
26	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
27	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
28	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
29	chr6:162080897..162083173-chr6:162084992..162086582,2	K562	blood:
30	chr6:162001523..162004451-chr6:162007412..162009361,2	K562	blood:
31	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
32	chr19:35885081..35886581-chr6:162062521..162064392,2	K562	blood:
33	chr6:161965795..161968097-chr6:161969436..161971580,2	K562	blood:
34	chr6:162022910..162024654-chr6:162024740..162027099,2	K562	blood:
35	chr6:161962166..161963929-chr6:161965968..161968206,2	K562	blood:
36	chr6:161813445..161815530-chr6:162115453..162117705,2	MCF-7	breast:
37	chr6:161966825..161970007-chr6:161974073..161976606,3	K562	blood:
38	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
39	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPAT4-2	chr6:161984667-161986399	NONHSAT115940

No data

Variant related genes	Relation type
ENSG00000221021	TF binding region
ENSG00000221021	CpG island

Extended variants
information (count: 8793 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:8793 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55696762	chr6:161961958-161961959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185765877	chr6:161961974-161961975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566515326	chr6:161962022-161962023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534638062	chr6:161962030-161962031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530665204	chr6:161962035-161962036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190390025	chr6:161962084-161962085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147932729	chr6:161962095-161962096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141821997	chr6:161962109-161962110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568670	chr6:161962121-161962122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs573750372	chr6:161962134-161962135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536268253	chr6:161962157-161962158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370862589	chr6:161962162-161962163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182601321	chr6:161962177-161962178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545420214	chr6:161962190-161962191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367757397	chr6:161962199-161962200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145685734	chr6:161962207-161962208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188576850	chr6:161962251-161962252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12198150	chr6:161962311-161962312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191811769	chr6:161962314-161962315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75929701	chr6:161962332-161962333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55845596	chr6:161962355-161962356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61082056	chr6:161962369-161962370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183877525	chr6:161962400-161962401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147662046	chr6:161962463-161962464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73593435	chr6:161962468-161962469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571472084	chr6:161962478-161962479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188931266	chr6:161962513-161962514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535412832	chr6:161962522-161962523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191334855	chr6:161962534-161962535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149147832	chr6:161962547-161962548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536400104	chr6:161962567-161962568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553095707	chr6:161962580-161962581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555002187	chr6:161962581-161962582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572759513	chr6:161962591-161962592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183737647	chr6:161962593-161962594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186578310	chr6:161962681-161962682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143285650	chr6:161962682-161962683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191864516	chr6:161962689-161962690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371053262	chr6:161962691-161962692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374106737	chr6:161962730-161962731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148337746	chr6:161962746-161962747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540366228	chr6:161962785-161962786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568730932	chr6:161962786-161962787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560590135	chr6:161962801-161962802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377289961	chr6:161962811-161962812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183951570	chr6:161962839-161962840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565049271	chr6:161962843-161962844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530859177	chr6:161962852-161962853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200159092	chr6:161962859-161962860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190021774	chr6:161962865-161962866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161957800-161963400	Weak transcription	HSMM	muscle
2	chr6:161957800-161968800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:161963200-161964200	Enhancers	Fetal Brain Male	brain
4	chr6:161963400-161963800	Enhancers	HSMMtube	muscle
5	chr6:161963400-161964400	Enhancers	HSMM	muscle
6	chr6:161964400-161965000	Enhancers	Fetal Brain Female	brain
7	chr6:161964800-161965200	Enhancers	GM12878-XiMat	blood
8	chr6:161965200-161965600	Weak transcription	GM12878-XiMat	blood
9	chr6:161965600-161968000	Enhancers	GM12878-XiMat	blood
10	chr6:161967000-161971000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:161968400-161969200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:161968400-161970200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:161968400-161971600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:161968600-161968800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:161968600-161969200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:161968600-161969200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:161968600-161970000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr6:161968800-161969000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:161968800-161969000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:161968800-161969200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:161968800-161969800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr6:161969200-161970000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr6:161969200-161971000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr6:161969400-161969800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:161969800-161970200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr6:161969800-161970200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:161969800-161970200	Enhancers	Esophagus	oesophagus
28	chr6:161969800-161970200	Enhancers	Right Atrium	heart
29	chr6:161970000-161970200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:161970200-161970600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:161970200-161970800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr6:161970600-161971800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:161970800-161971400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:161971000-161971200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:161971000-161971200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:161971000-161971400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:161971000-161971400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:161971400-161971800	Active TSS	A549	lung
39	chr6:161971800-161973800	Weak transcription	A549	lung
40	chr6:161975800-161976800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:161978000-161981600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr6:161978800-161980800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:161979800-161980600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:161983400-161983800	Enhancers	Colon Smooth Muscle	Colon
45	chr6:161988400-161990200	Weak transcription	Aorta	Aorta
46	chr6:161990200-161990800	Strong transcription	Aorta	Aorta
47	chr6:161990800-161991000	ZNF genes & repeats	Aorta	Aorta
48	chr6:161995200-161995600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:161995600-161996000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:161995800-161996400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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