Variant report

Variant	nsv883528
Chromosome Location	chr6:29447724-29494897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:1467)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29459520-29459683	K562	blood:	n/a	n/a
2	ATF1	chr6:29465238-29465245	K562	blood:	n/a	n/a
3	ATF1	chr6:29484009-29484209	K562	blood:	n/a	n/a
4	ATF1	chr6:29459294-29459754	K562	blood:	n/a	n/a
5	ATF1	chr6:29458475-29458935	K562	blood:	n/a	n/a
6	BACH1	chr6:29455457-29455787	K562	blood:	n/a	n/a
7	BHLHE40	chr6:29477112-29477348	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:29478160-29478319	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:29467541-29467772	K562	blood:	n/a	n/a
10	BHLHE40	chr6:29478030-29478400	K562	blood:	n/a	n/a
11	BHLHE40	chr6:29458370-29458968	K562	blood:	n/a	n/a
12	BHLHE40	chr6:29459289-29459713	K562	blood:	n/a	n/a
13	BRCA1	chr6:29476984-29477087	GM12878	blood:	n/a	n/a
14	CBX3	chr6:29483750-29484388	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:29483797-29484274	HCT-116	colon:	n/a	n/a
16	CCNT2	chr6:29458160-29458786	K562	blood:	n/a	n/a
17	CEBPB	chr6:29461104-29461374	IMR90	lung:	n/a	chr6:29461222-29461233
18	CEBPB	chr6:29492820-29493375	K562	blood:	n/a	chr6:29493216-29493227
19	CEBPB	chr6:29468925-29469256	IMR90	lung:	n/a	chr6:29469074-29469087 chr6:29469076-29469085 chr6:29469074-29469085 chr6:29469075-29469086
20	CEBPB	chr6:29470090-29470222	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:29461156-29461405	MCF-7	breast:	n/a	chr6:29461222-29461233
22	CEBPB	chr6:29492851-29493397	H1-hESC	embryonic stem cell:	n/a	chr6:29493216-29493227
23	CEBPB	chr6:29493070-29493392	IMR90	lung:	n/a	chr6:29493216-29493227
24	CEBPB	chr6:29468890-29469252	MCF-7	breast:	n/a	chr6:29469074-29469087 chr6:29469076-29469085 chr6:29469074-29469085 chr6:29469075-29469086
25	CEBPB	chr6:29451556-29451893	HepG2	liver:	n/a	chr6:29451728-29451739
26	CEBPB	chr6:29490658-29490690	K562	blood:	n/a	n/a
27	CEBPB	chr6:29468924-29469249	K562	blood:	n/a	chr6:29469074-29469087 chr6:29469076-29469085 chr6:29469074-29469085 chr6:29469075-29469086
28	CEBPB	chr6:29493070-29493404	HepG2	liver:	n/a	chr6:29493216-29493227
29	CEBPB	chr6:29458480-29458729	K562	blood:	n/a	n/a
30	CEBPB	chr6:29461057-29461393	H1-hESC	embryonic stem cell:	n/a	chr6:29461222-29461233
31	CEBPB	chr6:29468894-29469267	HepG2	liver:	n/a	chr6:29469074-29469087 chr6:29469076-29469085 chr6:29469074-29469085 chr6:29469075-29469086
32	CEBPB	chr6:29493083-29493346	A549	lung:	n/a	chr6:29493216-29493227
33	CEBPB	chr6:29461058-29461389	HepG2	liver:	n/a	chr6:29461222-29461233
34	CEBPB	chr6:29461061-29461396	K562	blood:	n/a	chr6:29461222-29461233
35	CEBPB	chr6:29458273-29458675	K562	blood:	n/a	n/a
36	CEBPB	chr6:29461154-29461365	Hela-S3	cervix:	n/a	chr6:29461222-29461233
37	CEBPB	chr6:29461146-29461284	K562	blood:	n/a	chr6:29461222-29461233
38	CEBPB	chr6:29451583-29451872	A549	lung:	n/a	chr6:29451728-29451739
39	CEBPB	chr6:29451605-29451865	MCF-7	breast:	n/a	chr6:29451728-29451739
40	CEBPD	chr6:29458474-29458869	K562	blood:	n/a	n/a
41	CHD2	chr6:29455143-29455242	HepG2	liver:	n/a	n/a
42	CTCF	chr6:29478060-29478210	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr6:29478080-29478230	GM12878	blood:	n/a	n/a
44	CTCF	chr6:29455140-29455290	GM06990	blood:	n/a	n/a
45	CTCF	chr6:29478100-29478250	GM12871	blood:	n/a	n/a
46	CTCF	chr6:29477266-29477341	GM12891	blood:	n/a	n/a
47	CTCF	chr6:29478110-29478286	K562	blood:	n/a	n/a
48	CTCF	chr6:29478080-29478230	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr6:29478188-29478282	LNCaP	prostate:	n/a	n/a
50	CTCF	chr6:29478002-29478337	K562	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29455126-29455176	RPTEC	kidney:	n/a
2	chr6:29457094-29457144	AG04449	skin:	fetal
3	chr6:29454755-29454805	T-47D	breast:	n/a
4	chr6:29455126-29455176	RPTEC	kidney:	n/a
5	chr6:29457094-29457144	AG04449	skin:	fetal
6	chr6:29454755-29454805	T-47D	breast:	n/a
7	chr6:29454873-29454923	NT2-D1	testis:	n/a
8	chr6:29461584-29461634	NHDF-neo	bronchial:	n/a
9	chr6:29456563-29456613	NHBE	bronchial:	n/a
10	chr6:29457094-29457144	K562	blood:	n/a
11	chr6:29456577-29456627	IMR90	lung:	fetal
12	chr6:29455126-29455176	HEK293	kidney:	embryo
13	chr6:29455331-29455381	HRCEpiC	kidney:	n/a
14	chr6:29454873-29454923	ProgFib	skin:	n/a
15	chr6:29456162-29456212	HUVEC	blood vessel:	n/a
16	chr6:29461549-29461599	HepG2	liver:	n/a
17	chr6:29457282-29457332	PANC-1	pancreas:	n/a
18	chr6:29461584-29461634	NH-A	brain:	n/a
19	chr6:29461549-29461599	HUVEC	blood vessel:	n/a
20	chr6:29456611-29456661	SAEC	small airway:	n/a
21	chr6:29455532-29455582	ECC-1	luminal epithelium:	n/a
22	chr6:29454954-29455004	HNPCEpiC	eye:	n/a
23	chr6:29455512-29455562	BE2_C	brain:	n/a
24	chr6:29454623-29454673	GM12891	blood:	n/a
25	chr6:29455322-29455372	NHBE	bronchial:	n/a
26	chr6:29454888-29454938	U87	brain:	n/a
27	chr6:29456577-29456627	GM12891	blood:	n/a
28	chr6:29455365-29455415	AG10803	skin:	n/a
29	chr6:29455331-29455381	HCF	heart:	n/a
30	chr6:29456611-29456661	H1-hESC	embryonic stem cell:	embryo
31	chr6:29457282-29457332	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:29454672-29454722	U87	brain:	n/a
33	chr6:29456162-29456212	HNPCEpiC	eye:	n/a
34	chr6:29457282-29457332	IMR90	lung:	fetal
35	chr6:29455331-29455381	A549	lung:	n/a
36	chr6:29455331-29455381	PrEC	prostate:	n/a
37	chr6:29461584-29461634	Jurkat	blood:	n/a
38	chr6:29456162-29456212	A549	lung:	n/a
39	chr6:29456563-29456613	SKMC	muscle:	n/a
40	chr6:29454888-29454938	AG04450	lung:	fetal
41	chr6:29461549-29461599	U87	brain:	n/a
42	chr6:29455256-29455306	GM12878	blood:	n/a
43	chr6:29455532-29455582	HCT-116	colon:	n/a
44	chr6:29455302-29455352	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:29461269-29461319	GM12891	blood:	n/a
46	chr6:29457282-29457332	PrEC	prostate:	n/a
47	chr6:29454888-29454938	HEK293	kidney:	embryo
48	chr6:29454623-29454673	Hela-S3	cervix:	n/a
49	chr6:29455256-29455306	AG04450	lung:	fetal
50	chr6:29454954-29455004	AG10803	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29460358..29463035-chr6:29483811..29485363,2	K562	blood:
2	chr6:29454260..29456802-chr6:29460764..29462349,2	K562	blood:
3	chr6:29434261..29435839-chr6:29452792..29455620,2	K562	blood:
4	chr6:29469820..29472263-chr6:29475289..29476878,2	MCF-7	breast:
5	chr6:29490586..29492205-chr6:29493882..29496471,2	K562	blood:
6	chr6:29470497..29473606-chr6:29476660..29479341,3	K562	blood:
7	chr6:29484816..29486671-chr6:29489047..29491131,2	K562	blood:
8	chr6:29484816..29486671-chr6:29489047..29491131,2	K562	blood:
9	chr6:29457898..29460263-chr6:29462415..29464583,2	K562	blood:
10	chr6:29477552..29479306-chr6:29484098..29486256,2	K562	blood:
11	chr6:29483683..29485672-chr6:29497592..29500057,2	K562	blood:
12	chr6:29430057..29432693-chr6:29447492..29449143,2	K562	blood:
13	chr6:29481318..29483910-chr6:29486622..29489549,2	K562	blood:
14	chr6:29494254..29496248-chr6:29505741..29508107,2	K562	blood:
15	chr6:29394189..29395109-chr6:29478134..29478678,2	MCF-7	breast:
16	chr6:29490586..29492205-chr6:29493882..29496471,2	K562	blood:
17	chr6:29457898..29460263-chr6:29462415..29464583,2	K562	blood:
18	chr6:29481318..29483910-chr6:29486622..29489549,2	K562	blood:
19	chr6:29460358..29463035-chr6:29483811..29485363,2	K562	blood:
20	chr6:29477552..29479306-chr6:29484098..29486256,2	K562	blood:
21	chr6:29469820..29472263-chr6:29475289..29476878,2	MCF-7	breast:
22	chr6:29470497..29473606-chr6:29476660..29479341,3	K562	blood:

No data

Variant related genes	Relation type
LINC01015	TF binding region
MAS1L	TF binding region
MAS1LP1	TF binding region
ENSG00000229274	TF binding region
RPS17P1	TF binding region
LINC01015	CpG island
MAS1L	CpG island
MAS1LP1	CpG island
ENSG00000229274	CpG island
RPS17P1	CpG island
ENSG00000229281	chromatin interactions
ENSG00000204687	chromatin interactions

Extended variants
information (count: 1446 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7767061	chr6:29447724-29447725	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190432125	chr6:29447753-29447754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560646438	chr6:29447754-29447755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555049618	chr6:29447759-29447760	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs574232636	chr6:29447845-29447846	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs555230688	chr6:29450889-29450890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575172119	chr6:29450913-29450914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192837676	chr6:29450997-29450998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553852899	chr6:29451031-29451032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184718157	chr6:29451074-29451075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189654194	chr6:29451099-29451100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562631550	chr6:29451107-29451108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576174540	chr6:29451119-29451120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541600735	chr6:29451122-29451123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571844369	chr6:29451144-29451145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139688907	chr6:29451167-29451168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2107189	chr6:29451168-29451169	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs116283377	chr6:29451251-29451252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192242542	chr6:29451261-29451262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532934239	chr6:29451276-29451277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142959930	chr6:29451293-29451294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146141096	chr6:29451302-29451303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560466205	chr6:29451317-29451318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184821927	chr6:29451357-29451358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189193686	chr6:29451429-29451430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568659791	chr6:29451450-29451451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140001368	chr6:29451488-29451489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149870619	chr6:29451498-29451499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554456417	chr6:29451529-29451530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373493064	chr6:29451632-29451633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181611727	chr6:29451642-29451643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556164766	chr6:29451693-29451694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144885472	chr6:29451773-29451774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541932907	chr6:29451801-29451802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs118077891	chr6:29451845-29451846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112464414	chr6:29451876-29451877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540911432	chr6:29451892-29451893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115571294	chr6:29451927-29451928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533105001	chr6:29451954-29451955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562084733	chr6:29451971-29451972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543428460	chr6:29451988-29451989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11756628	chr6:29451999-29452000	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs189944515	chr6:29452003-29452004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75901489	chr6:29452005-29452006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374791682	chr6:29452086-29452087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113271806	chr6:29452088-29452089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568520233	chr6:29452108-29452109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1234844	chr6:29452136-29452137	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs142113123	chr6:29452144-29452145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147799336	chr6:29452181-29452182	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29450800-29451600	Enhancers	NH-A	brain
2	chr6:29451200-29452200	Enhancers	Liver	Liver
3	chr6:29452200-29457000	Weak transcription	Liver	Liver
4	chr6:29454000-29455600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:29454200-29454800	Enhancers	Primary hematopoietic stem cells	blood
6	chr6:29454200-29455000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr6:29454200-29455400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:29454400-29456000	Enhancers	K562	blood
9	chr6:29454800-29457800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:29455000-29457200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:29455400-29457200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:29455600-29457200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:29456000-29457800	Weak transcription	K562	blood
14	chr6:29457000-29457400	Enhancers	Liver	Liver
15	chr6:29457200-29458000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:29457200-29459400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr6:29457200-29461200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:29457800-29458600	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr6:29457800-29459800	Enhancers	Primary hematopoietic stem cells	blood
20	chr6:29457800-29459800	Enhancers	K562	blood
21	chr6:29458000-29459000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:29459000-29459600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr6:29459000-29461200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:29459400-29462200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:29459800-29460200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:29459800-29461800	Weak transcription	K562	blood
27	chr6:29460200-29461000	Enhancers	Primary hematopoietic stem cells	blood
28	chr6:29461800-29462400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:29461800-29462600	Enhancers	K562	blood
30	chr6:29462200-29462400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr6:29464000-29464400	Enhancers	K562	blood
32	chr6:29468200-29468400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:29468400-29468600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:29468600-29496200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:29469800-29471400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:29469800-29471400	Enhancers	NH-A	brain
37	chr6:29470000-29470200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:29470200-29470600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:29470200-29470600	Enhancers	NHEK	skin
40	chr6:29470200-29470800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:29470200-29471200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:29470200-29471200	Enhancers	NHDF-Ad	bronchial
43	chr6:29470400-29471000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:29472800-29473200	Enhancers	HepG2	liver
45	chr6:29475200-29477800	Enhancers	GM12878-XiMat	blood
46	chr6:29475600-29475800	Enhancers	HSMMtube	muscle
47	chr6:29475800-29476000	Flanking Active TSS	HSMMtube	muscle
48	chr6:29476800-29481600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:29477400-29478800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:29477400-29478800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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