Variant report

Variant	esv1851714
Chromosome Location	chr6:31948757-32011522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:3236)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
2	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:32007706-32008062	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
6	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
7	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
8	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
9	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
10	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
11	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
12	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
13	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
14	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
15	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
16	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
17	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
18	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
19	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
20	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
21	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
22	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
23	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
24	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
25	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
26	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
27	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
28	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
29	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
30	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
31	CTCF	chr6:31990362-31990415	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:31960420-31960464	Medullo	brain:	n/a	n/a
33	CTCF	chr6:31950068-31950071	GM19240	blood:	n/a	n/a
34	CTCF	chr6:31975020-31975170	HepG2	liver:	n/a	n/a
35	CTCF	chr6:32007726-32007926	HepG2	liver:	n/a	n/a
36	CTCF	chr6:31973475-31973543	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:32008734-32008854	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr6:31957626-31957645	K562	blood:	n/a	n/a
39	CTCF	chr6:31979963-31980021	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr6:31973412-31973562	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:31982918-31982945	GM12878	blood:	n/a	n/a
42	CTCF	chr6:31971424-31971464	GM10266	blood:	n/a	n/a
43	CTCF	chr6:31996865-31996870	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:31957202-31957484	Medullo	brain:	n/a	n/a
45	CTCF	chr6:31982815-31982922	GM20000	blood:	n/a	n/a
46	CTCF	chr6:32007860-32008010	HepG2	liver:	n/a	n/a
47	CTCF	chr6:31989984-31990184	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr6:31989985-31990147	Lung_OC	lung:	n/a	n/a
49	CTCF	chr6:32006160-32006257	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:31950049-31950157	Hela-S3	cervix:	n/a	n/a

(count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32010333-32010383	HCT-116	colon:	n/a
2	chr6:31974906-31974956	PFSK-1	brain:	n/a
3	chr6:31980046-31980096	HCM	heart:	n/a
4	chr6:32010333-32010383	HCT-116	colon:	n/a
5	chr6:31974906-31974956	PFSK-1	brain:	n/a
6	chr6:31980046-31980096	HCM	heart:	n/a
7	chr6:31964193-31964243	GM19239	blood:	n/a
8	chr6:31997491-31997541	HepG2	liver:	n/a
9	chr6:31996931-31996981	T-47D	breast:	n/a
10	chr6:31973255-31973305	U87	brain:	n/a
11	chr6:32007986-32008036	GM19239	blood:	n/a
12	chr6:31974906-31974956	HepG2	liver:	n/a
13	chr6:31980043-31980093	NHDF-neo	bronchial:	n/a
14	chr6:31978789-31978839	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:31973051-31973101	SK-N-SH_RA	brain:	n/a
16	chr6:31980043-31980093	IMR90	lung:	fetal
17	chr6:31977506-31977556	GM06990	blood:	n/a
18	chr6:31963892-31963942	GM12891	blood:	n/a
19	chr6:31963892-31963942	BJ	skin:	n/a
20	chr6:31997026-31997076	Jurkat	blood:	n/a
21	chr6:31963912-31963962	HNPCEpiC	eye:	n/a
22	chr6:31964754-31964804	CMK	blood:	n/a
23	chr6:31997491-31997541	GM12892	blood:	n/a
24	chr6:31973255-31973305	NHDF-neo	bronchial:	n/a
25	chr6:31973255-31973305	Caco-2	colon:	n/a
26	chr6:31963892-31963942	AG09319	gingival:	n/a
27	chr6:32006951-32007001	HEEpiC	esophagus:	n/a
28	chr6:31997491-31997541	NHBE	bronchial:	n/a
29	chr6:31977443-31977493	HRCEpiC	kidney:	n/a
30	chr6:31996657-31996707	HEK293	kidney:	embryo
31	chr6:31980046-31980096	HepG2	liver:	n/a
32	chr6:32010240-32010290	HRCEpiC	kidney:	n/a
33	chr6:32009422-32009472	AG09319	gingival:	n/a
34	chr6:32005786-32005836	H1-hESC	embryonic stem cell:	embryo
35	chr6:31978789-31978839	Caco-2	colon:	n/a
36	chr6:31964315-31964365	SK-N-SH	brain:	n/a
37	chr6:31977599-31977649	AG04449	skin:	fetal
38	chr6:31997067-31997117	Caco-2	colon:	n/a
39	chr6:32006951-32007001	HAEpiC	amniotic membrane:	n/a
40	chr6:32011506-32011556	HRE	kidney:	n/a
41	chr6:32006079-32006129	PFSK-1	brain:	n/a
42	chr6:32010178-32010228	AG09319	gingival:	n/a
43	chr6:31997067-31997117	NHDF-neo	bronchial:	n/a
44	chr6:31997059-31997109	T-47D	breast:	n/a
45	chr6:31973345-31973395	HCF	heart:	n/a
46	chr6:31980856-31980906	HNPCEpiC	eye:	n/a
47	chr6:31997026-31997076	MCF-7	breast:	n/a
48	chr6:31997491-31997541	NT2-D1	testis:	n/a
49	chr6:32009283-32009333	AG09319	gingival:	n/a
50	chr6:31996657-31996707	HNPCEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
2	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
3	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
4	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNXB-6	chr6:32000490-32002082	ENSG00000229776.1
2	lnc-DOM3Z-2	chr6:31967753-31969345	ENSG00000233627.2
3	lnc-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1
4	lnc-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STK19	hsa-miR-29c-3p	chr6:31949085-31949105
2	STK19	hsa-miR-29c-3p	chr6:31981823-31981843

Variant related genes	Relation type
TNXA	TF binding region
STK19P	TF binding region
CYP21A1P	TF binding region
C4B	TF binding region
C4B-AS1	TF binding region
CYP21A2	TF binding region
ENSG00000268923	TF binding region
TNXB	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A1P	CpG island
C4B	CpG island
C4B-AS1	CpG island
CYP21A2	CpG island
ENSG00000268923	CpG island
TNXB	CpG island
C4A-AS1	CpG island
C4A	CpG island
ENSG00000166278	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204344	chromatin interactions

Extended variants
information (count: 975 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56337326	chr6:31949352-31949353	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs112291543	chr6:31949636-31949637	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148404715	chr6:31949688-31949689	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs56386803	chr6:31950266-31950267	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200199167	chr6:31950335-31950336	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs142556478	chr6:31950651-31950652	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs56001408	chr6:31951207-31951208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56261921	chr6:31951367-31951368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567402938	chr6:31951502-31951503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55954268	chr6:31951912-31951913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150969927	chr6:31952180-31952181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140897509	chr6:31952255-31952256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144856589	chr6:31952806-31952807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147934048	chr6:31952857-31952858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141809751	chr6:31952957-31952958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150064392	chr6:31952980-31952981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145187627	chr6:31953172-31953173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56009677	chr6:31953467-31953468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55809101	chr6:31954348-31954349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202084040	chr6:31955186-31955187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55744710	chr6:31955274-31955275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111070454	chr6:31955572-31955573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144254624	chr6:31955619-31955620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149150903	chr6:31955712-31955713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56285587	chr6:31956424-31956425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143279658	chr6:31956473-31956474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546861494	chr6:31958703-31958704	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs55822911	chr6:31958960-31958961	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs62404830	chr6:31959002-31959003	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs56307180	chr6:31959480-31959481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138900138	chr6:31959714-31959715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56369909	chr6:31960770-31960771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs113306459	chr6:31960866-31960867	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs140619911	chr6:31961797-31961798	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144749273	chr6:31961904-31961905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138671842	chr6:31961917-31961918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202167626	chr6:31961985-31961986	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200048885	chr6:31962004-31962005	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200946182	chr6:31962012-31962013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567857665	chr6:31962033-31962034	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201969273	chr6:31962044-31962045	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs538011679	chr6:31962061-31962062	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200426958	chr6:31962100-31962101	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201536871	chr6:31962141-31962142	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374202211	chr6:31962172-31962173	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs377339156	chr6:31962174-31962175	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs200442104	chr6:31962236-31962237	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556729650	chr6:31962286-31962287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs575217817	chr6:31962333-31962334	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs545908174	chr6:31962343-31962344	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	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
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
2	chr6:31941000-31949800	Weak transcription	Gastric	stomach
3	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:31941400-31949000	Weak transcription	Colonic Mucosa	Colon
8	chr6:31941400-31949400	Weak transcription	Primary B cells from cord blood	blood
9	chr6:31941400-31949400	Weak transcription	NH-A	brain
10	chr6:31941400-31950000	Weak transcription	Fetal Kidney	kidney
11	chr6:31941600-31949200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:31941600-31949200	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:31941600-31950000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr6:31941800-31950000	Weak transcription	Dnd41	blood
15	chr6:31947400-31949400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:31947800-31950000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:31948000-31949400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:31948000-31949600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr6:31948000-31949600	Weak transcription	GM12878-XiMat	blood
20	chr6:31948000-31950000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:31948200-31949800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31948200-31949800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:31948200-31949800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr6:31948200-31949800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr6:31948200-31949800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:31948200-31949800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:31948200-31949800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:31948200-31949800	Weak transcription	Fetal Lung	lung
29	chr6:31948200-31949800	Weak transcription	Placenta	Placenta
30	chr6:31948200-31949800	Weak transcription	HSMM	muscle
31	chr6:31948200-31949800	Weak transcription	HSMMtube	muscle
32	chr6:31948200-31949800	Weak transcription	NHEK	skin
33	chr6:31948200-31950000	Weak transcription	Primary B cells from peripheral blood	blood
34	chr6:31948200-31950000	Weak transcription	Brain Substantia Nigra	brain
35	chr6:31948200-31966000	Weak transcription	Pancreas	Pancrea
36	chr6:31948400-31949200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:31948400-31949400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr6:31948400-31949400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:31948400-31949800	Weak transcription	Primary T cells from cord blood	blood
40	chr6:31948400-31949800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr6:31948400-31949800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr6:31948400-31950000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:31948400-31950000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:31948400-31950000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:31948400-31950000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:31948400-31950000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:31948400-31950000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:31948400-31950000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:31948400-31950000	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr6:31948400-31950000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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