Variant report

Variant	esv1799840
Chromosome Location	chr6:20196549-20210374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:20202223-20202827	K562	blood:	n/a	n/a
2	ATF2	chr6:20208854-20209313	GM12878	blood:	n/a	n/a
3	ATF2	chr6:20201971-20202560	GM12878	blood:	n/a	n/a
4	ATF2	chr6:20202046-20202565	GM12878	blood:	n/a	n/a
5	ATF3	chr6:20202188-20202559	K562	blood:	n/a	n/a
6	BACH1	chr6:20202248-20202539	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:20202211-20202568	K562	blood:	n/a	n/a
8	BATF	chr6:20202184-20202438	GM12878	blood:	n/a	chr6:20202384-20202395 chr6:20202385-20202395 chr6:20202322-20202331
9	BATF	chr6:20208961-20209288	GM12878	blood:	n/a	chr6:20209184-20209195
10	BATF	chr6:20202174-20202540	GM12878	blood:	n/a	chr6:20202384-20202395 chr6:20202385-20202395 chr6:20202322-20202331
11	BATF	chr6:20201060-20201398	GM12878	blood:	n/a	n/a
12	BATF	chr6:20198428-20198733	GM12878	blood:	n/a	chr6:20198558-20198567
13	BATF	chr6:20208994-20209324	GM12878	blood:	n/a	chr6:20209184-20209195
14	BATF	chr6:20198472-20198683	GM12878	blood:	n/a	chr6:20198558-20198567
15	BCL11A	chr6:20202121-20202468	GM12878	blood:	n/a	chr6:20202240-20202253
16	BCL3	chr6:20202156-20202456	GM12878	blood:	n/a	chr6:20202240-20202253
17	BCLAF1	chr6:20202143-20202525	GM12878	blood:	n/a	chr6:20202240-20202253
18	BHLHE40	chr6:20209059-20209259	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:20202193-20202724	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:20204315-20204969	K562	blood:	n/a	chr6:20204515-20204524 chr6:20204509-20204530 chr6:20204514-20204523 chr6:20204515-20204524
21	BHLHE40	chr6:20204159-20204676	GM12878	blood:	n/a	chr6:20204515-20204524 chr6:20204509-20204530 chr6:20204514-20204523 chr6:20204515-20204524
22	BHLHE40	chr6:20198500-20198791	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:20206029-20206408	K562	blood:	n/a	n/a
24	BHLHE40	chr6:20205602-20205659	K562	blood:	n/a	n/a
25	CBX3	chr6:20202242-20202629	HCT-116	colon:	n/a	n/a
26	CBX3	chr6:20202177-20202583	HCT-116	colon:	n/a	n/a
27	CCNT2	chr6:20202289-20202376	K562	blood:	n/a	n/a
28	CCNT2	chr6:20204463-20204701	K562	blood:	n/a	n/a
29	CCNT2	chr6:20203660-20203666	K562	blood:	n/a	n/a
30	CEBPB	chr6:20202210-20202450	K562	blood:	n/a	n/a
31	CEBPB	chr6:20202046-20202575	HCT-116	colon:	n/a	n/a
32	CEBPB	chr6:20202201-20202487	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:20201015-20201490	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:20201036-20201377	K562	blood:	n/a	n/a
35	CEBPB	chr6:20201963-20202724	HCT-116	colon:	n/a	n/a
36	CEBPB	chr6:20202139-20202548	K562	blood:	n/a	n/a
37	CEBPB	chr6:20202136-20202665	A549	lung:	n/a	n/a
38	CEBPB	chr6:20202241-20202477	A549	lung:	n/a	n/a
39	CEBPB	chr6:20202150-20202540	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:20201054-20201400	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:20202154-20202536	K562	blood:	n/a	n/a
42	CEBPB	chr6:20202165-20202527	A549	lung:	n/a	n/a
43	CEBPB	chr6:20202103-20202681	GM12878	blood:	n/a	n/a
44	CEBPB	chr6:20202272-20202431	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:20200862-20201516	MCF-7	breast:	n/a	n/a
46	CEBPB	chr6:20202225-20202489	MCF-7	breast:	n/a	n/a
47	CEBPB	chr6:20202233-20202428	HepG2	liver:	n/a	n/a
48	CHD2	chr6:20202171-20202477	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr6:20209064-20209210	GM12878	blood:	n/a	n/a
50	CTCF	chr6:20200760-20200910	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:20209127-20209177	BE2_C	brain:	n/a
2	chr6:20209127-20209177	AG09319	gingival:	n/a
3	chr6:20209127-20209177	AG09309	skin:	n/a
4	chr6:20209127-20209177	Hela-S3	cervix:	n/a
5	chr6:20209127-20209177	GM19239	blood:	n/a
6	chr6:20209127-20209177	HepG2	liver:	n/a
7	chr6:20209127-20209177	PrEC	prostate:	n/a
8	chr6:20209127-20209177	K562	blood:	n/a
9	chr6:20209127-20209177	LNCaP	prostate:	n/a
10	chr6:20209127-20209177	HIPEpiC	eye:	n/a
11	chr6:20209127-20209177	GM06990	blood:	n/a
12	chr6:20209127-20209177	T-47D	breast:	n/a
13	chr6:20209127-20209177	SK-N-SH_RA	brain:	n/a
14	chr6:20209127-20209177	GM12892	blood:	n/a
15	chr6:20209127-20209177	SK-N-SH	brain:	n/a
16	chr6:20209127-20209177	SAEC	small airway:	n/a
17	chr6:20209127-20209177	HEK293	kidney:	embryo
18	chr6:20209127-20209177	NHBE	bronchial:	n/a
19	chr6:20209127-20209177	HCPEpiC	choroid plexus:	n/a
20	chr6:20209127-20209177	HEEpiC	esophagus:	n/a
21	chr6:20209127-20209177	AG04449	skin:	fetal
22	chr6:20209127-20209177	H1-hESC	embryonic stem cell:	embryo
23	chr6:20209127-20209177	HAEpiC	amniotic membrane:	n/a
24	chr6:20209127-20209177	HL-60	blood:	n/a
25	chr6:20209127-20209177	U87	brain:	n/a
26	chr6:20209127-20209177	IMR90	lung:	fetal
27	chr6:20209127-20209177	HRCEpiC	kidney:	n/a
28	chr6:20209127-20209177	AG10803	skin:	n/a
29	chr6:20209127-20209177	Jurkat	blood:	n/a
30	chr6:20209127-20209177	NHDF-neo	bronchial:	n/a
31	chr6:20209127-20209177	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:20209127-20209177	RPTEC	kidney:	n/a
33	chr6:20209127-20209177	NT2-D1	testis:	n/a
34	chr6:20209127-20209177	SK-N-MC	brain:	n/a
35	chr6:20209127-20209177	CMK	blood:	n/a
36	chr6:20209127-20209177	ProgFib	skin:	n/a
37	chr6:20209127-20209177	HUVEC	blood vessel:	n/a
38	chr6:20209127-20209177	MCF-7	breast:	n/a
39	chr6:20209127-20209177	HNPCEpiC	eye:	n/a
40	chr6:20209127-20209177	AG04450	lung:	fetal
41	chr6:20209127-20209177	BJ	skin:	n/a
42	chr6:20209127-20209177	HCM	heart:	n/a
43	chr6:20209127-20209177	HRE	kidney:	n/a
44	chr6:20209127-20209177	MCF10A-Er-Src	breast:	n/a
45	chr6:20209127-20209177	GM12891	blood:	n/a
46	chr6:20209127-20209177	AoSMC	blood vessel:	n/a
47	chr6:20209127-20209177	PFSK-1	brain:	n/a
48	chr6:20209127-20209177	HCT-116	colon:	n/a
49	chr6:20209127-20209177	NB4	blood:	n/a
50	chr6:20209127-20209177	HCF	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:20183379..20185644-chr6:20202802..20204808,2	K562	blood:
2	chr6:20201120..20201764-chr6:20210706..20211232,2	MCF-7	breast:
3	chr6:20199968..20202569-chr6:20401397..20403351,2	MCF-7	breast:
4	chr6:20200700..20201255-chr6:20210255..20211078,3	MCF-7	breast:
5	chr6:20199116..20200755-chr6:20209336..20210921,2	K562	blood:
6	chr6:20208632..20214725-chr6:20400593..20405219,15	K562	blood:
7	chr6:20199925..20202970-chr6:20211369..20213429,3	MCF-7	breast:
8	chr6:20117949..20119536-chr6:20206647..20209362,2	MCF-7	breast:
9	chr6:20126269..20128367-chr6:20209873..20212157,2	MCF-7	breast:
10	chr2:25300005..25301584-chr6:20210003..20211589,2	MCF-7	breast:
11	chr6:20209069..20211986-chr6:20231381..20233005,2	K562	blood:
12	chr6:20195556..20197935-chr6:20198781..20201333,3	K562	blood:
13	chr6:20208250..20214334-chr6:20400294..20406447,14	K562	blood:
14	chr6:20207945..20211455-chr6:26105249..26107952,3	MCF-7	breast:
15	chr6:20204116..20205859-chr6:20336022..20338444,2	K562	blood:
16	chr6:20195556..20197935-chr6:20198781..20201333,3	K562	blood:
17	chr6:20199116..20200755-chr6:20209336..20210921,2	K562	blood:
18	chr6:20198875..20206310-chr6:20399680..20405305,15	K562	blood:
19	chr6:20201447..20207053-chr6:20401187..20404960,5	K562	blood:
20	chr6:20200700..20201255-chr6:20210255..20211078,3	MCF-7	breast:
21	chr20:52840503..52842605-chr6:20208710..20211532,2	MCF-7	breast:
22	chr6:20208057..20215931-chr6:20401288..20405953,13	MCF-7	breast:
23	chr6:20182072..20183869-chr6:20199499..20201801,2	MCF-7	breast:
24	chr6:20180103..20182906-chr6:20201581..20203746,2	K562	blood:
25	chr6:20206158..20207867-chr6:20401632..20403613,2	MCF-7	breast:
26	chr6:20193176..20194693-chr6:20195772..20197789,2	K562	blood:
27	chr6:20198811..20199394-chr6:20211686..20212534,2	K562	blood:
28	chr6:20203563..20206976-chr6:20208756..20213535,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000227803	TF binding region
ENSG00000227803	CpG island
ENSG00000227803	chromatin interactions
ENSG00000112242	chromatin interactions
ENSG00000172197	chromatin interactions

Extended variants
information (count: 491 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566637887	chr6:20196581-20196582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533795193	chr6:20196587-20196588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558610612	chr6:20196668-20196669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569727924	chr6:20196676-20196677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147323822	chr6:20196677-20196678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6926099	chr6:20196696-20196697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4712461	chr6:20196823-20196824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192270663	chr6:20196860-20196861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141071681	chr6:20196861-20196862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537013872	chr6:20196863-20196864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559009896	chr6:20196866-20196867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527881460	chr6:20196887-20196888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571153149	chr6:20196890-20196891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546091509	chr6:20196922-20196923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4712462	chr6:20196934-20196935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531866346	chr6:20196957-20196958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553570358	chr6:20196976-20196977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59534126	chr6:20196991-20196992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575082710	chr6:20196993-20196994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550167287	chr6:20197017-20197018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553964597	chr6:20197046-20197047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568450040	chr6:20197079-20197080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58418526	chr6:20197094-20197095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373895262	chr6:20197100-20197101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113013220	chr6:20197101-20197102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548463279	chr6:20197104-20197105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72826629	chr6:20197113-20197114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs113515838	chr6:20197117-20197118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188605075	chr6:20197126-20197127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570184032	chr6:20197135-20197136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537560803	chr6:20197218-20197219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192839216	chr6:20197257-20197258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574071438	chr6:20197322-20197323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377622422	chr6:20197352-20197353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs398084802	chr6:20197361-20197362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535124604	chr6:20197362-20197363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148513285	chr6:20197371-20197372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572655558	chr6:20197389-20197390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543412089	chr6:20197419-20197420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546352902	chr6:20197422-20197423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7767027	chr6:20197425-20197426	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs182616139	chr6:20197427-20197428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543913753	chr6:20197429-20197430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373051829	chr6:20197445-20197446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562211831	chr6:20197468-20197469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529296550	chr6:20197476-20197477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547482304	chr6:20197508-20197509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12665157	chr6:20197513-20197514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369134172	chr6:20197516-20197517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4710923	chr6:20197537-20197538	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian cancer	20844748	CNVD
Developmental delay	19490664	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:20139600-20201200	Weak transcription	Fetal Lung	lung
2	chr6:20171200-20198600	Weak transcription	Adipose Nuclei	Adipose
3	chr6:20175000-20201800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr6:20175000-20205200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:20175200-20202000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:20182000-20204400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:20183600-20204200	Weak transcription	Right Atrium	heart
8	chr6:20184000-20198600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr6:20184200-20198600	Weak transcription	Colon Smooth Muscle	Colon
10	chr6:20184400-20202400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:20184600-20200800	Weak transcription	Hela-S3	cervix
12	chr6:20187200-20199000	Weak transcription	Fetal Stomach	stomach
13	chr6:20187200-20201000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:20187600-20201600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr6:20187600-20204400	Weak transcription	Lung	lung
16	chr6:20187800-20197600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr6:20187800-20203000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:20188800-20198800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:20188800-20200600	Weak transcription	Dnd41	blood
20	chr6:20189400-20200200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:20189400-20200400	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr6:20191800-20197400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:20192000-20198600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr6:20192000-20200600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:20192000-20200600	Weak transcription	Pancreas	Pancrea
26	chr6:20192000-20201200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr6:20192600-20197800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:20192800-20197400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:20192800-20199800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr6:20193000-20197600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:20193000-20198600	Weak transcription	Colonic Mucosa	Colon
32	chr6:20193000-20209200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr6:20193200-20197400	Weak transcription	GM12878-XiMat	blood
34	chr6:20193200-20197600	Weak transcription	Fetal Heart	heart
35	chr6:20193200-20198600	Weak transcription	Fetal Intestine Large	intestine
36	chr6:20193200-20198600	Weak transcription	Ovary	ovary
37	chr6:20193200-20198600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr6:20193200-20200600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr6:20193200-20200800	Weak transcription	K562	blood
40	chr6:20193200-20201200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr6:20193200-20204200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:20193200-20204200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:20193400-20200800	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:20193800-20197800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr6:20195600-20198800	Weak transcription	Small Intestine	intestine
46	chr6:20195600-20200800	Weak transcription	Gastric	stomach
47	chr6:20196000-20198600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr6:20196200-20200800	Weak transcription	Right Ventricle	heart
49	chr6:20196400-20198600	Weak transcription	Fetal Intestine Small	intestine
50	chr6:20196400-20200600	Weak transcription	Stomach Mucosa	stomach

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