Variant report

Variant	nsv884578
Chromosome Location	chr6:31950266-32011480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:702)
CpG islands
(count:3178)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:702 , 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	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:32007706-32008062	HepG2	liver:	n/a	n/a
5	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
6	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
7	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
8	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
9	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
10	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
11	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
12	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
13	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
14	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
15	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
16	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
17	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
18	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
19	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
20	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
21	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
22	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
23	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
24	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
25	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
26	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
27	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
28	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
29	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
30	CTCF	chr6:31984864-31984882	GM10266	blood:	n/a	n/a
31	CTCF	chr6:31976032-31976040	LNCaP	prostate:	n/a	n/a
32	CTCF	chr6:32006159-32006305	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr6:31964085-31964142	Hela-S3	cervix:	n/a	chr6:31964112-31964133 chr6:31964119-31964132 chr6:31964117-31964135
34	CTCF	chr6:31982830-31982894	HepG2	liver:	n/a	n/a
35	CTCF	chr6:31957348-31957448	GM10266	blood:	n/a	n/a
36	CTCF	chr6:31984851-31984858	GM10266	blood:	n/a	n/a
37	CTCF	chr6:31996871-31996889	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:31957269-31957418	GM12878	blood:	n/a	n/a
39	CTCF	chr6:31982867-31982879	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr6:31989991-31990175	LNCaP	prostate:	n/a	n/a
41	CTCF	chr6:31975052-31975153	A549	lung:	n/a	n/a
42	CTCF	chr6:31990314-31990438	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:31957067-31957570	K562	blood:	n/a	n/a
44	CTCF	chr6:32007819-32007886	Gliobla	brain:	n/a	n/a
45	CTCF	chr6:31989929-31990291	K562	blood:	n/a	n/a
46	CTCF	chr6:31973412-31973562	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:31974983-31975159	HepG2	liver:	n/a	n/a
48	CTCF	chr6:32006160-32006257	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:31996811-31996913	HepG2	liver:	n/a	chr6:31996855-31996873 chr6:31996857-31996870 chr6:31996850-31996871
50	CTCF	chr6:31975120-31975270	HCPEpiC	choroid plexus:	n/a	n/a

(count:3178 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32007916-32007966	GM12891	blood:	n/a
2	chr6:31973051-31973101	HMEC	breast:	n/a
3	chr6:32006079-32006129	GM12891	blood:	n/a
4	chr6:32010327-32010377	AG10803	skin:	n/a
5	chr6:31996931-31996981	MCF10A-Er-Src	breast:	n/a
6	chr6:31974906-31974956	SKMC	muscle:	n/a
7	chr6:32007916-32007966	GM12891	blood:	n/a
8	chr6:31973051-31973101	HMEC	breast:	n/a
9	chr6:32006079-32006129	GM12891	blood:	n/a
10	chr6:32010327-32010377	AG10803	skin:	n/a
11	chr6:31996931-31996981	MCF10A-Er-Src	breast:	n/a
12	chr6:31974906-31974956	SKMC	muscle:	n/a
13	chr6:31980856-31980906	Hela-S3	cervix:	n/a
14	chr6:31964193-31964243	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:32009283-32009333	SKMC	muscle:	n/a
16	chr6:32009283-32009333	HRPEpiC	eye:	n/a
17	chr6:31973255-31973305	PANC-1	pancreas:	n/a
18	chr6:31997026-31997076	IMR90	lung:	fetal
19	chr6:31973255-31973305	NH-A	brain:	n/a
20	chr6:31980836-31980886	GM19239	blood:	n/a
21	chr6:32007625-32007675	AG09309	skin:	n/a
22	chr6:32007916-32007966	AG04449	skin:	fetal
23	chr6:32009422-32009472	SK-N-SH_RA	brain:	n/a
24	chr6:31980856-31980906	LNCaP	prostate:	n/a
25	chr6:31964391-31964441	AG10803	skin:	n/a
26	chr6:31976720-31976770	ECC-1	luminal epithelium:	n/a
27	chr6:31964193-31964243	NT2-D1	testis:	n/a
28	chr6:31974906-31974956	RPTEC	kidney:	n/a
29	chr6:31980836-31980886	AoSMC	blood vessel:	n/a
30	chr6:31977599-31977649	HEEpiC	esophagus:	n/a
31	chr6:31980043-31980093	CMK	blood:	n/a
32	chr6:31976720-31976770	SKMC	muscle:	n/a
33	chr6:31976548-31976598	MCF-7	breast:	n/a
34	chr6:31980043-31980093	AG04449	skin:	fetal
35	chr6:31973345-31973395	BE2_C	brain:	n/a
36	chr6:31964274-31964324	GM12891	blood:	n/a
37	chr6:31996931-31996981	K562	blood:	n/a
38	chr6:31977443-31977493	PrEC	prostate:	n/a
39	chr6:32005897-32005947	AG09309	skin:	n/a
40	chr6:31996657-31996707	HRPEpiC	eye:	n/a
41	chr6:31978789-31978839	Hela-S3	cervix:	n/a
42	chr6:31980052-31980102	ProgFib	skin:	n/a
43	chr6:32006079-32006129	HAEpiC	amniotic membrane:	n/a
44	chr6:31973255-31973305	AG10803	skin:	n/a
45	chr6:32007625-32007675	AG09319	gingival:	n/a
46	chr6:32007986-32008036	NB4	blood:	n/a
47	chr6:32007986-32008036	AG10803	skin:	n/a
48	chr6:31980856-31980906	MCF-7	breast:	n/a
49	chr6:31997564-31997614	HRE	kidney:	n/a
50	chr6:31977506-31977556	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	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-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1
3	lnc-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2
4	lnc-DOM3Z-2	chr6:31967753-31969345	ENSG00000233627.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	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
ENSG00000204366	chromatin interactions
ENSG00000166278	chromatin interactions

Extended variants
information (count: 966 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:966 , 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	rs56386803	chr6:31950266-31950267	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200199167	chr6:31950335-31950336	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142556478	chr6:31950651-31950652	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs56001408	chr6:31951207-31951208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56261921	chr6:31951367-31951368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567402938	chr6:31951502-31951503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs55954268	chr6:31951912-31951913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150969927	chr6:31952180-31952181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140897509	chr6:31952255-31952256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144856589	chr6:31952806-31952807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147934048	chr6:31952857-31952858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141809751	chr6:31952957-31952958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150064392	chr6:31952980-31952981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145187627	chr6:31953172-31953173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56009677	chr6:31953467-31953468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs55809101	chr6:31954348-31954349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs202084040	chr6:31955186-31955187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs55744710	chr6:31955274-31955275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111070454	chr6:31955572-31955573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144254624	chr6:31955619-31955620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149150903	chr6:31955712-31955713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56285587	chr6:31956424-31956425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143279658	chr6:31956473-31956474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546861494	chr6:31958703-31958704	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs55822911	chr6:31958960-31958961	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62404830	chr6:31959002-31959003	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs56307180	chr6:31959480-31959481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138900138	chr6:31959714-31959715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56369909	chr6:31960770-31960771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs113306459	chr6:31960866-31960867	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs140619911	chr6:31961797-31961798	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs144749273	chr6:31961904-31961905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138671842	chr6:31961917-31961918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202167626	chr6:31961985-31961986	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200048885	chr6:31962004-31962005	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200946182	chr6:31962012-31962013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567857665	chr6:31962033-31962034	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201969273	chr6:31962044-31962045	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs538011679	chr6:31962061-31962062	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200426958	chr6:31962100-31962101	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201536871	chr6:31962141-31962142	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374202211	chr6:31962172-31962173	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs377339156	chr6:31962174-31962175	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200442104	chr6:31962236-31962237	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556729650	chr6:31962286-31962287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575217817	chr6:31962333-31962334	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs545908174	chr6:31962343-31962344	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs557313902	chr6:31962354-31962355	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs377362766	chr6:31962366-31962367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs572543424	chr6:31962393-31962394	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:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31948200-31966000	Weak transcription	Pancreas	Pancrea
2	chr6:31948400-31950400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:31948400-31950400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:31948400-31950400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:31948400-31950400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:31948400-31950400	Weak transcription	Brain Anterior Caudate	brain
7	chr6:31948400-31950400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:31948400-31950400	Weak transcription	Esophagus	oesophagus
9	chr6:31948400-31950400	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:31948400-31950600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:31948400-31966000	Weak transcription	Adipose Nuclei	Adipose
12	chr6:31948400-31967000	Weak transcription	Ovary	ovary
13	chr6:31948400-31973400	Weak transcription	Lung	lung
14	chr6:31948600-31951200	Weak transcription	Fetal Stomach	stomach
15	chr6:31948600-31966400	Weak transcription	Fetal Intestine Small	intestine
16	chr6:31962200-31962400	Enhancers	Liver	Liver
17	chr6:31962400-31963600	Weak transcription	Liver	Liver
18	chr6:31963600-31964400	Enhancers	Liver	Liver
19	chr6:31972200-31973200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:31972200-31973400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr6:31972200-31974200	Enhancers	Primary T cells fromperipheralblood	blood
22	chr6:31972200-31974200	Enhancers	HepG2	liver
23	chr6:31972400-31972800	Enhancers	Primary B cells from peripheral blood	blood
24	chr6:31972400-31972800	Enhancers	Thymus	Thymus
25	chr6:31972400-31973400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr6:31972400-31973400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr6:31972400-31973400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr6:31972400-31973400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:31972400-31973400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr6:31972400-31974800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr6:31972600-31972800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr6:31972600-31973200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr6:31972600-31973200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:31972600-31973400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr6:31972600-31973400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:31973000-31973400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:31973400-31973600	Enhancers	Lung	lung
38	chr6:31974200-31974800	Weak transcription	HepG2	liver
39	chr6:31974800-31975000	Enhancers	HepG2	liver
40	chr6:31974800-31975200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr6:31975000-31978800	Weak transcription	HepG2	liver
42	chr6:31975200-31975400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr6:31975400-31976400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr6:31976400-31976800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr6:31976800-31978600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr6:31978600-31978800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr6:31978600-31979000	Enhancers	Ovary	ovary
48	chr6:31978800-31979000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr6:31978800-31979200	Enhancers	Liver	Liver
50	chr6:31978800-31979200	Enhancers	HepG2	liver

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