Variant report

Variant	nsv519981
Chromosome Location	chr17:33841737-33864479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 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	BACH1	chr17:33860323-33860430	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr17:33846924-33847412	GM12878	blood:	n/a	n/a
3	BATF	chr17:33847073-33847406	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:33847092-33847361	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:33847021-33847496	GM12878	blood:	n/a	n/a
6	BCLAF1	chr17:33860290-33860714	GM12878	blood:	n/a	n/a
7	BCLAF1	chr17:33864461-33865044	GM12878	blood:	n/a	n/a
8	BCLAF1	chr17:33860286-33860774	GM12878	blood:	n/a	n/a
9	BHLHE40	chr17:33860332-33860715	GM12878	blood:	n/a	n/a
10	BRCA1	chr17:33860381-33860629	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr17:33850438-33850691	A549	lung:	n/a	chr17:33850542-33850553
12	CEBPB	chr17:33863813-33863906	H1-hESC	embryonic stem cell:	n/a	chr17:33863871-33863882
13	CEBPB	chr17:33863705-33863942	HepG2	liver:	n/a	chr17:33863871-33863882
14	CEBPB	chr17:33850401-33850654	HepG2	liver:	n/a	chr17:33850542-33850553
15	CEBPB	chr17:33860411-33860626	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr17:33863685-33863955	IMR90	lung:	n/a	chr17:33863871-33863882
17	CEBPB	chr17:33863826-33863905	Hela-S3	cervix:	n/a	chr17:33863871-33863882
18	CEBPB	chr17:33863668-33864066	K562	blood:	n/a	chr17:33863871-33863882
19	CEBPB	chr17:33863692-33863941	A549	lung:	n/a	chr17:33863871-33863882
20	CHD1	chr17:33863991-33865028	GM12878	blood:	n/a	n/a
21	CTCF	chr17:33860291-33860695	K562	blood:	n/a	n/a
22	CTCF	chr17:33860369-33860664	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr17:33860460-33860610	HPF	lung:	n/a	n/a
24	CTCF	chr17:33860440-33860590	GM12869	blood:	n/a	n/a
25	CTCF	chr17:33860402-33860650	HepG2	liver:	n/a	n/a
26	CTCF	chr17:33860420-33860570	GM12867	blood:	n/a	n/a
27	CTCF	chr17:33860375-33860683	Gliobla	brain:	n/a	n/a
28	CTCF	chr17:33860239-33860724	HepG2	liver:	n/a	n/a
29	CTCF	chr17:33860115-33860865	A549	lung:	n/a	n/a
30	CTCF	chr17:33860440-33860590	GM12864	blood:	n/a	n/a
31	CTCF	chr17:33860290-33860662	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr17:33860261-33860895	SK-N-SH	brain:	n/a	n/a
33	CTCF	chr17:33860287-33860745	K562	blood:	n/a	n/a
34	CTCF	chr17:33860440-33860590	HCT-116	colon:	n/a	n/a
35	CTCF	chr17:33860414-33860615	Fibrobl	skin:	n/a	n/a
36	CTCF	chr17:33860420-33860570	AG04449	skin:	n/a	n/a
37	CTCF	chr17:33860225-33860793	K562	blood:	n/a	n/a
38	CTCF	chr17:33860385-33860654	GM12878	blood:	n/a	n/a
39	CTCF	chr17:33860460-33860610	AG09309	skin:	n/a	n/a
40	CTCF	chr17:33860420-33860570	BJ	skin:	n/a	n/a
41	CTCF	chr17:33860313-33860738	IMR90	lung:	n/a	n/a
42	CTCF	chr17:33860971-33861002	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr17:33860416-33860636	GM13976	blood:	n/a	n/a
44	CTCF	chr17:33860460-33860610	BE2_C	brain:	n/a	n/a
45	CTCF	chr17:33860420-33860570	HVMF	connective:	n/a	n/a
46	CTCF	chr17:33860460-33860610	HMEC	breast:	n/a	n/a
47	CTCF	chr17:33860460-33860610	GM12871	blood:	n/a	n/a
48	CTCF	chr17:33860172-33860881	HCT-116	colon:	n/a	n/a
49	CTCF	chr17:33860328-33860698	T-47D	breast:	n/a	n/a
50	CTCF	chr17:33860460-33860610	HCFaa	heart:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33842255-33842305	AoSMC	blood vessel:	n/a
2	chr17:33842181-33842231	SKMC	muscle:	n/a
3	chr17:33842301-33842351	AG04450	lung:	fetal
4	chr17:33842255-33842305	T-47D	breast:	n/a
5	chr17:33842181-33842231	HNPCEpiC	eye:	n/a
6	chr17:33842255-33842305	SAEC	small airway:	n/a
7	chr17:33842181-33842231	HCF	heart:	n/a
8	chr17:33842181-33842231	Hepatocyte	liver:	n/a
9	chr17:33842255-33842305	HAEpiC	amniotic membrane:	n/a
10	chr17:33842301-33842351	A549	lung:	n/a
11	chr17:33842255-33842305	RPTEC	kidney:	n/a
12	chr17:33842181-33842231	HAEpiC	amniotic membrane:	n/a
13	chr17:33842301-33842351	HAEpiC	amniotic membrane:	n/a
14	chr17:33842181-33842231	HPAEpiC	pulmonary alveolar:	n/a
15	chr17:33842181-33842231	GM12878	blood:	n/a
16	chr17:33842301-33842351	HEK293	kidney:	embryo
17	chr17:33842301-33842351	IMR90	lung:	fetal
18	chr17:33842301-33842351	AG10803	skin:	n/a
19	chr17:33842301-33842351	T-47D	breast:	n/a
20	chr17:33842301-33842351	HIPEpiC	eye:	n/a
21	chr17:33842255-33842305	HEEpiC	esophagus:	n/a
22	chr17:33842301-33842351	GM06990	blood:	n/a
23	chr17:33842181-33842231	HMEC	breast:	n/a
24	chr17:33842255-33842305	HCM	heart:	n/a
25	chr17:33842255-33842305	MCF10A-Er-Src	breast:	n/a
26	chr17:33842181-33842231	HRCEpiC	kidney:	n/a
27	chr17:33842255-33842305	AG10803	skin:	n/a
28	chr17:33842181-33842231	A549	lung:	n/a
29	chr17:33842301-33842351	HCM	heart:	n/a
30	chr17:33842301-33842351	SK-N-SH	brain:	n/a
31	chr17:33842301-33842351	ProgFib	skin:	n/a
32	chr17:33842181-33842231	SK-N-MC	brain:	n/a
33	chr17:33842301-33842351	SAEC	small airway:	n/a
34	chr17:33842255-33842305	GM12891	blood:	n/a
35	chr17:33842255-33842305	HIPEpiC	eye:	n/a
36	chr17:33842255-33842305	U87	brain:	n/a
37	chr17:33842255-33842305	BJ	skin:	n/a
38	chr17:33842181-33842231	MCF10A-Er-Src	breast:	n/a
39	chr17:33842301-33842351	BJ	skin:	n/a
40	chr17:33842255-33842305	NH-A	brain:	n/a
41	chr17:33842181-33842231	NHDF-neo	bronchial:	n/a
42	chr17:33842301-33842351	Caco-2	colon:	n/a
43	chr17:33842255-33842305	SK-N-MC	brain:	n/a
44	chr17:33842181-33842231	K562	blood:	n/a
45	chr17:33842301-33842351	GM12878	blood:	n/a
46	chr17:33842181-33842231	H1-hESC	embryonic stem cell:	embryo
47	chr17:33842181-33842231	AG09319	gingival:	n/a
48	chr17:33842255-33842305	NB4	blood:	n/a
49	chr17:33842301-33842351	HMEC	breast:	n/a
50	chr17:33842181-33842231	AG09309	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33498739..33499644-chr17:33860109..33860877,2	K562	blood:
2	chr17:33836676..33838220-chr17:33863138..33865744,2	K562	blood:
3	chr17:33639415..33640336-chr17:33860071..33860985,4	K562	blood:
4	chr17:33639516..33640351-chr17:33860065..33861379,3	MCF-7	breast:
5	chr17:33639164..33640312-chr17:33859981..33861014,10	MCF-7	breast:
6	chr17:33498244..33499072-chr17:33859971..33860594,3	MCF-7	breast:
7	chr17:33469068..33470787-chr17:33848506..33850097,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN14-1	chr17:33861076-33861349	l_1431_chr17:33860158-33861349_placenta
2	lnc-SLFN14-1	chr17:33861396-33861597	l_1431_chr17:33860158-33861349_placenta
3	lnc-SLFN14-1	chr17:33860159-33860493	l_1431_chr17:33860158-33861349_placenta
4	lnc-SLFN14-1	chr17:33862088-33862198	l_1431_chr17:33860158-33861349_placenta
5	lnc-SLFN14-1	chr17:33861941-33861965	l_1431_chr17:33860158-33861349_placenta

No data

Variant related genes	Relation type
ENSG00000267074	TF binding region
ENSG00000255987	TF binding region
ENSG00000267074	CpG island
ENSG00000255987	CpG island
ENSG00000267074	chromatin interactions
ENSG00000073536	chromatin interactions

Extended variants
information (count: 880 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12450474	chr17:33841737-33841738	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34006651	chr17:33841742-33841743	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191376123	chr17:33841768-33841769	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs80063592	chr17:33841793-33841794	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564781884	chr17:33841797-33841798	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532825781	chr17:33841865-33841866	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs182770821	chr17:33841871-33841872	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs569460873	chr17:33841879-33841880	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs535132467	chr17:33841917-33841918	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs28526116	chr17:33841977-33841978	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs538217722	chr17:33842021-33842022	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186010054	chr17:33842024-33842025	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376120227	chr17:33842114-33842115	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577859148	chr17:33842132-33842133	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563850820	chr17:33842137-33842138	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147650994	chr17:33842190-33842191	Strong transcription Genic enhancers Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs529547038	chr17:33842209-33842210	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs8077662	chr17:33842228-33842229	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576617548	chr17:33842236-33842237	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76591819	chr17:33842244-33842245	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562287764	chr17:33842252-33842253	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572583146	chr17:33842278-33842279	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs371009378	chr17:33842287-33842288	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs375788085	chr17:33842292-33842293	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs541600961	chr17:33842319-33842320	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs192080940	chr17:33842438-33842439	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139793364	chr17:33842440-33842441	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183270593	chr17:33842467-33842468	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562904809	chr17:33842501-33842502	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34616612	chr17:33842507-33842508	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528971046	chr17:33842599-33842600	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115115306	chr17:33842614-33842615	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565752130	chr17:33842643-33842644	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58481344	chr17:33842672-33842673	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75438365	chr17:33842675-33842676	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534555493	chr17:33842700-33842701	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377628650	chr17:33842726-33842727	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570974022	chr17:33842738-33842739	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571452441	chr17:33842771-33842772	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114162310	chr17:33842783-33842784	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376091999	chr17:33842809-33842810	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556609978	chr17:33842821-33842822	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187595472	chr17:33842823-33842824	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145228949	chr17:33842847-33842848	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555617476	chr17:33842883-33842884	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191973148	chr17:33842897-33842898	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572495690	chr17:33842940-33842941	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541311682	chr17:33842941-33842942	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558286374	chr17:33842948-33842949	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578195614	chr17:33842950-33842951	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	21569311	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33835400-33849600	Weak transcription	Spleen	Spleen
2	chr17:33836400-33843800	Strong transcription	Dnd41	blood
3	chr17:33837800-33846800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr17:33839000-33841800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr17:33839800-33841800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr17:33839800-33842200	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr17:33840000-33842200	Strong transcription	GM12878-XiMat	blood
8	chr17:33840000-33843400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr17:33840400-33841800	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr17:33840400-33841800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:33840400-33842200	Strong transcription	Primary T cells from cord blood	blood
12	chr17:33840800-33841800	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr17:33841000-33841800	Enhancers	Fetal Lung	lung
14	chr17:33841200-33842000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr17:33841200-33842000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr17:33841200-33842000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
17	chr17:33841200-33843400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
18	chr17:33841600-33842000	Enhancers	Duodenum Mucosa	Duodenum
19	chr17:33841600-33842400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr17:33841600-33842400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr17:33841600-33843400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr17:33841800-33842000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr17:33841800-33842000	Flanking Active TSS	Fetal Lung	lung
24	chr17:33841800-33842000	Bivalent Enhancer	Fetal Stomach	stomach
25	chr17:33841800-33842400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
26	chr17:33841800-33842600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
27	chr17:33841800-33843000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:33841800-33844200	Genic enhancers	Primary T cells fromperipheralblood	blood
29	chr17:33842000-33842200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr17:33842000-33842200	Enhancers	Fetal Lung	lung
31	chr17:33842000-33843000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr17:33842000-33843000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr17:33842000-33843200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr17:33842200-33842400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr17:33842200-33843200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr17:33842200-33846000	Weak transcription	GM12878-XiMat	blood
37	chr17:33842200-33846400	Weak transcription	Primary T cells from cord blood	blood
38	chr17:33842400-33842800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr17:33842400-33843200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr17:33842400-33843200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr17:33842400-33847200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr17:33842600-33844400	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr17:33842800-33848200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr17:33843000-33843200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:33843000-33843200	Bivalent Enhancer	Fetal Lung	lung
46	chr17:33843000-33844000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr17:33843000-33846800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr17:33843200-33843800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr17:33843200-33844200	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr17:33843200-33844800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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