Variant report

Variant	nsv970345
Chromosome Location	chr6:106871018-106894266
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	ARID3A	chr6:106894067-106894548	HepG2	liver:	n/a	n/a
2	ATF2	chr6:106892765-106893102	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:106892804-106893114	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr6:106887260-106887717	MCF-7	breast:	n/a	n/a
5	CEBPB	chr6:106892802-106893143	A549	lung:	n/a	n/a
6	CEBPB	chr6:106892790-106893105	K562	blood:	n/a	n/a
7	CEBPB	chr6:106892529-106893153	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:106892807-106893129	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:106892785-106893218	MCF-7	breast:	n/a	n/a
10	CEBPB	chr6:106892791-106893139	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:106892731-106893135	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:106889985-106890229	Hela-S3	cervix:	n/a	chr6:106890063-106890074
13	CTCF	chr6:106892920-106893070	WERI-Rb-1	eye:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
14	CTCF	chr6:106892940-106893090	HMEC	breast:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
15	CTCF	chr6:106894000-106894150	BJ	skin:	n/a	n/a
16	CTCF	chr6:106893820-106893970	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr6:106894240-106894390	HMF	breast:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
18	CTCF	chr6:106894260-106894410	HMF	breast:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
19	CTCF	chr6:106893840-106893990	HMF	breast:	n/a	n/a
20	CTCF	chr6:106892880-106893030	HepG2	liver:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
21	CTCF	chr6:106894220-106894370	GM12867	blood:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
22	CTCF	chr6:106892900-106893050	SAEC	small airway:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
23	CTCF	chr6:106892980-106893130	A549	lung:	n/a	n/a
24	CTCF	chr6:106892822-106893127	T-47D	breast:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
25	CTCF	chr6:106894120-106894270	NHLF	lung:	n/a	n/a
26	CTCF	chr6:106892920-106893070	GM12873	blood:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
27	CTCF	chr6:106894260-106894410	GM12865	blood:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
28	CTCF	chr6:106892880-106893030	NHLF	lung:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
29	CTCF	chr6:106894180-106894330	HPF	lung:	n/a	n/a
30	CTCF	chr6:106893920-106894070	GM12873	blood:	n/a	n/a
31	CTCF	chr6:106892580-106892730	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr6:106892880-106893030	SAEC	small airway:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
33	CTCF	chr6:106892960-106893110	MCF-7	breast:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
34	CTCF	chr6:106892753-106893198	HepG2	liver:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
35	CTCF	chr6:106892900-106893050	HAc	cerebellar:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
36	CTCF	chr6:106892846-106893117	ECC-1	luminal epithelium:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
37	CTCF	chr6:106894240-106894390	HCM	heart:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
38	CTCF	chr6:106892808-106893094	A549	lung:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
39	CTCF	chr6:106892940-106893090	HEEpiC	esophagus:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
40	CTCF	chr6:106892823-106893097	ECC-1	luminal epithelium:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
41	CTCF	chr6:106893700-106893850	GM12872	blood:	n/a	n/a
42	CTCF	chr6:106892892-106893079	GM13976	blood:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
43	CTCF	chr6:106894083-106894660	IMR90	lung:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
44	CTCF	chr6:106894240-106894390	AG10803	skin:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
45	CTCF	chr6:106892900-106893050	HPAF	blood vessel:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
46	CTCF	chr6:106892940-106893090	AG09309	skin:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
47	CTCF	chr6:106894220-106894370	GM12874	blood:	n/a	chr6:106894339-106894357 chr6:106894341-106894362
48	CTCF	chr6:106892900-106893050	GM12864	blood:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997
49	CTCF	chr6:106894140-106894290	RPTEC	kidney:	n/a	n/a
50	CTCF	chr6:106892900-106893050	GM12873	blood:	n/a	chr6:106892974-106892992 chr6:106892979-106892987 chr6:106892975-106892991 chr6:106892976-106892997

No.	Distal block	Cell Line	Cell type
1	chr6:106893928..106895248-chr6:107013534..107015064,5	MCF-7	breast:
2	chr6:106887436..106888995-chr6:106894077..106896594,2	K562	blood:
3	chr19:15039996..15040603-chr6:106892565..106893251,2	MCF-7	breast:
4	chr6:106806640..106811296-chr6:106885915..106890564,7	MCF-7	breast:
5	chr6:106807586..106809435-chr6:106889467..106891139,2	MCF-7	breast:
6	chr6:106893452..106894012-chr6:106997057..106997774,2	MCF-7	breast:
7	chr6:106786932..106787612-chr6:106892577..106893519,3	MCF-7	breast:
8	chr6:106891408..106894325-chr6:107016587..107019305,2	MCF-7	breast:
9	chr6:106793639..106796605-chr6:106892288..106895627,3	MCF-7	breast:
10	chr6:106893993..106894791-chr6:107013993..107015233,6	K562	blood:
11	chr6:106893943..106894830-chr6:107003943..107005243,5	MCF-7	breast:
12	chr6:106892949..106893527-chr6:107011363..107012186,2	K562	blood:
13	chr6:106860820..106863674-chr6:106869273..106872080,2	MCF-7	breast:
14	chr6:106806608..106808537-chr6:106892921..106895314,2	MCF-7	breast:
15	chr6:106782426..106783382-chr6:106892777..106893307,2	MCF-7	breast:
16	chr6:106807797..106809564-chr6:106892316..106894790,2	MCF-7	breast:
17	chr6:106891526..106894302-chr6:106895961..106897783,2	K562	blood:
18	chr6:106770748..106773743-chr6:106892839..106894795,2	MCF-7	breast:
19	chr6:106887436..106888995-chr6:106894077..106896594,2	K562	blood:
20	chr6:106807932..106809126-chr6:106892501..106893325,3	MCF-7	breast:
21	chr6:106892479..106893508-chr6:107003919..107004825,3	MCF-7	breast:
22	chr6:106807999..106808515-chr6:106892101..106893044,2	MCF-7	breast:
23	chr6:106782985..106783505-chr6:106892625..106893417,2	K562	blood:
24	chr6:106775261..106777423-chr6:106891472..106893784,2	MCF-7	breast:
25	chr6:106892895..106893435-chr6:107004443..107004986,2	MCF-7	breast:
26	chr6:106892627..106893526-chr6:107014079..107015028,6	K562	blood:
27	chr6:106884945..106886506-chr6:106958785..106960709,2	MCF-7	breast:
28	chr6:106842514..106845297-chr6:106886526..106889026,2	MCF-7	breast:
29	chr6:106858650..106860928-chr6:106870754..106873020,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG5-3	chr6:106872089-106872178	NONHSAT114235
2	lnc-ATG5-3	chr6:106884469-106884815	NONHSAT114235
3	lnc-ATG5-3	chr6:106872036-106872078	NONHSAT114235

Variant related genes	Relation type
RNA5SP211	TF binding region
ENSG00000202386	chromatin interactions
ENSG00000233941	chromatin interactions
ENSG00000112297	chromatin interactions
ENSG00000057663	chromatin interactions

Extended variants
information (count: 908 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549290172	chr6:106871030-106871031	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188259634	chr6:106871043-106871044	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376116971	chr6:106871048-106871049	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370627622	chr6:106871059-106871060	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192200800	chr6:106871106-106871107	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77353141	chr6:106871125-106871126	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397702619	chr6:106871127-106871128	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78351979	chr6:106871129-106871130	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79986728	chr6:106871130-106871131	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs5878887	chr6:106871149-106871150	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147003179	chr6:106871196-106871197	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147616991	chr6:106871228-106871229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537443131	chr6:106871261-106871262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs58609287	chr6:106871262-106871263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537163726	chr6:106871279-106871280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537250541	chr6:106871294-106871295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12660142	chr6:106871297-106871298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12209784	chr6:106871320-106871321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12209791	chr6:106871347-106871348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12209793	chr6:106871370-106871371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557185791	chr6:106871372-106871373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56874055	chr6:106871428-106871429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527880630	chr6:106871436-106871437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17066969	chr6:106871455-106871456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs151129312	chr6:106871460-106871461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535685674	chr6:106871473-106871474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555262030	chr6:106871524-106871525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143624607	chr6:106871567-106871568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370709293	chr6:106871570-106871571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572312170	chr6:106871609-106871610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189640361	chr6:106871632-106871633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564094991	chr6:106871647-106871648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116643212	chr6:106871649-106871650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543428549	chr6:106871671-106871672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552969562	chr6:106871672-106871673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12529138	chr6:106871688-106871689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs528977683	chr6:106871702-106871703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374748528	chr6:106871755-106871756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549595402	chr6:106871768-106871769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544577553	chr6:106871799-106871800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559649960	chr6:106871800-106871801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548100082	chr6:106871879-106871880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199767195	chr6:106871895-106871896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142118894	chr6:106871898-106871899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74927078	chr6:106871902-106871903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180786598	chr6:106871906-106871907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9384611	chr6:106871980-106871981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs12197928	chr6:106872036-106872037	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536304920	chr6:106872062-106872063	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs145943129	chr6:106872067-106872068	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	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
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106853200-106896000	Weak transcription	Esophagus	oesophagus
2	chr6:106864200-106874000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:106865400-106877600	Weak transcription	Fetal Intestine Large	intestine
4	chr6:106866000-106887800	Weak transcription	Pancreas	Pancrea
5	chr6:106867000-106877400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:106869400-106871200	Enhancers	NHEK	skin
7	chr6:106870800-106872800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:106870800-106879200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:106871000-106871200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:106871000-106872800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:106871000-106872800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:106871000-106872800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:106871000-106879600	Weak transcription	HMEC	breast
14	chr6:106871200-106879400	Weak transcription	NHEK	skin
15	chr6:106872800-106873200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:106872800-106873600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr6:106872800-106873800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:106872800-106874000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:106873000-106873400	Enhancers	Liver	Liver
20	chr6:106873400-106873800	Enhancers	Adipose Nuclei	Adipose
21	chr6:106873600-106874400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr6:106873800-106878200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:106874000-106874200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:106874000-106874800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:106874200-106875000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:106874400-106874800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr6:106874400-106875000	Enhancers	HSMMtube	muscle
28	chr6:106874800-106876600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:106875000-106879200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:106875600-106875800	Bivalent Enhancer	HSMM	muscle
31	chr6:106875600-106875800	Enhancers	NH-A	brain
32	chr6:106875800-106876000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
33	chr6:106876600-106876800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:106876800-106877200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:106877200-106877400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr6:106877400-106878600	Enhancers	Fetal Intestine Small	intestine
37	chr6:106877400-106887800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr6:106877600-106879800	Enhancers	Fetal Intestine Large	intestine
39	chr6:106878200-106878800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:106878400-106878800	Enhancers	HepG2	liver
41	chr6:106878600-106882000	Weak transcription	Fetal Intestine Small	intestine
42	chr6:106878800-106879200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:106879200-106879800	Enhancers	Liver	Liver
44	chr6:106879200-106880200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:106879200-106880400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr6:106879200-106880600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:106879400-106880600	Genic enhancers	NHEK	skin
48	chr6:106879600-106880000	Enhancers	HSMMtube	muscle
49	chr6:106879600-106880400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:106879600-106880600	Enhancers	HMEC	breast

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