Variant report

Variant	nsv932623
Chromosome Location	chr19:42370540-42378620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1024)
CpG islands
(count:0)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:42376933-42377643	GM12878	blood:	n/a	n/a
2	ATF2	chr19:42375693-42377792	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr19:42370283-42370739	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:42376989-42377584	GM12878	blood:	n/a	n/a
5	ATF2	chr19:42376990-42377699	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:42375575-42376674	GM12878	blood:	n/a	n/a
7	ATF2	chr19:42371947-42372207	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr19:42375571-42376734	GM12878	blood:	n/a	n/a
9	ATF3	chr19:42376942-42377795	A549	lung:	n/a	n/a
10	ATF3	chr19:42375596-42377854	A549	lung:	n/a	n/a
11	BACH1	chr19:42377400-42377555	K562	blood:	n/a	n/a
12	BATF	chr19:42375657-42375997	GM12878	blood:	n/a	n/a
13	BCL11A	chr19:42375647-42376027	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
14	BCL11A	chr19:42375560-42376716	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
15	BCL3	chr19:42375751-42376862	K562	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
16	BCL3	chr19:42371940-42373334	A549	lung:	n/a	chr19:42372990-42372999
17	BCL3	chr19:42375501-42378207	A549	lung:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
18	BCL3	chr19:42375848-42376691	K562	blood:	n/a	chr19:42375859-42375868
19	BCL3	chr19:42378248-42378904	A549	lung:	n/a	n/a
20	BCL3	chr19:42377150-42377689	GM12878	blood:	n/a	n/a
21	BCL3	chr19:42375633-42377727	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
22	BCL3	chr19:42375662-42376446	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
23	BCL3	chr19:42376465-42376815	GM12878	blood:	n/a	n/a
24	BCL3	chr19:42374177-42374979	A549	lung:	n/a	n/a
25	BCL3	chr19:42375598-42378168	A549	lung:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
26	BCL3	chr19:42370177-42370810	A549	lung:	n/a	n/a
27	BCL3	chr19:42373515-42374109	A549	lung:	n/a	n/a
28	BCLAF1	chr19:42375707-42376540	K562	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
29	BCLAF1	chr19:42375106-42377683	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
30	BCLAF1	chr19:42376989-42377737	GM12878	blood:	n/a	n/a
31	BCLAF1	chr19:42375683-42376281	K562	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
32	BCLAF1	chr19:42375552-42376783	GM12878	blood:	n/a	chr19:42375859-42375868 chr19:42375762-42375771
33	BHLHE40	chr19:42377270-42377599	K562	blood:	n/a	n/a
34	BHLHE40	chr19:42375633-42376250	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:42377224-42377587	GM12878	blood:	n/a	n/a
36	BRCA1	chr19:42377129-42377509	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr19:42376466-42376593	HepG2	liver:	n/a	n/a
38	BRCA1	chr19:42375907-42376209	HepG2	liver:	n/a	n/a
39	BRCA1	chr19:42377318-42377570	HepG2	liver:	n/a	n/a
40	BRCA1	chr19:42377285-42377583	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr19:42375654-42375799	GM12878	blood:	n/a	n/a
42	BRCA1	chr19:42377062-42377071	GM12878	blood:	n/a	n/a
43	CBX3	chr19:42375688-42376053	K562	blood:	n/a	n/a
44	CCNT2	chr19:42375850-42376407	K562	blood:	n/a	n/a
45	CEBPB	chr19:42375957-42377727	A549	lung:	n/a	n/a
46	CEBPB	chr19:42371013-42371118	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:42377251-42377661	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr19:42375585-42377610	GM12878	blood:	n/a	n/a
49	CEBPB	chr19:42377190-42377444	K562	blood:	n/a	n/a
50	CEBPB	chr19:42377151-42377545	Hela-S3	cervix:	n/a	n/a

No data

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:42374727..42377526-chr19:42531576..42534265,2	MCF-7	breast:
2	chr19:42354421..42356282-chr19:42374725..42377333,2	MCF-7	breast:
3	chr19:42375885..42381575-chr19:42432655..42439530,9	K562	blood:
4	chr19:42371951..42373649-chr19:42373763..42375308,2	MCF-7	breast:
5	chr19:42377260..42377774-chr19:42455449..42456424,2	MCF-7	breast:
6	chr19:42375921..42378052-chr19:42410713..42412528,2	MCF-7	breast:
7	chr19:42346995..42348950-chr19:42370547..42372069,2	K562	blood:
8	chr19:42378071..42380066-chr19:42429626..42432415,2	MCF-7	breast:
9	chr19:42377177..42378851-chr19:42479605..42481434,2	K562	blood:
10	chr19:42373353..42379670-chr19:42459996..42464717,12	K562	blood:
11	chr19:42373231..42374863-chr19:42378109..42381070,2	MCF-7	breast:
12	chr19:42378499..42381176-chr19:42422747..42425494,2	MCF-7	breast:
13	chr19:42373231..42374863-chr19:42378109..42381070,2	MCF-7	breast:
14	chr19:42368937..42370473-chr19:42375983..42377700,2	MCF-7	breast:
15	chr19:42376866..42377852-chr19:42461645..42462448,2	K562	blood:
16	chr19:42374905..42377918-chr19:42453712..42457623,5	K562	blood:
17	chr19:42377500..42380123-chr19:42404788..42407614,2	MCF-7	breast:
18	chr19:42375829..42377976-chr19:42413032..42416255,3	MCF-7	breast:
19	chr19:42367000..42368909-chr19:42375795..42378988,3	MCF-7	breast:
20	chr19:42374516..42376922-chr19:42442141..42445764,4	K562	blood:
21	chr19:42377202..42377808-chr19:42438762..42439328,2	MCF-7	breast:
22	chr19:42374905..42378139-chr19:42452312..42458975,8	K562	blood:
23	chr19:42374516..42378766-chr19:42444244..42446935,5	K562	blood:
24	chr19:42369015..42372839-chr19:42460520..42463128,4	K562	blood:
25	chr19:42311919..42314019-chr19:42373613..42376038,2	K562	blood:
26	chr19:42354940..42358615-chr19:42368975..42372693,4	K562	blood:
27	chr19:42375695..42377388-chr19:42406535..42408788,2	K562	blood:
28	chr19:42346920..42348959-chr19:42369071..42372047,3	K562	blood:
29	chr19:42377330..42377861-chr19:42461768..42462284,2	MCF-7	breast:
30	chr19:42377082..42377816-chr19:42455455..42456477,4	MCF-7	breast:
31	chr19:42377383..42379799-chr19:42454565..42456876,2	MCF-7	breast:
32	chr19:42311919..42314958-chr19:42372358..42376038,3	K562	blood:
33	chr19:42374823..42377954-chr19:42385843..42389445,4	MCF-7	breast:
34	chr19:42373799..42381047-chr19:42460989..42465067,14	K562	blood:
35	chr19:42354721..42357873-chr19:42369180..42372292,3	MCF-7	breast:
36	chr19:42370513..42373649-chr19:42375625..42377894,4	MCF-7	breast:
37	chr19:42376907..42377725-chr19:42462018..42462632,4	MCF-7	breast:
38	chr19:42370231..42372294-chr19:42382726..42385087,2	MCF-7	breast:
39	chr19:42369679..42372709-chr19:42429800..42433926,4	K562	blood:
40	chr19:42370513..42373649-chr19:42375625..42377894,4	MCF-7	breast:
41	chr19:42377503..42378200-chr2:28962182..28962711,2	HCT-116	colon:
42	chr19:42374489..42376013-chr8:101732709..101734886,2	MCF-7	breast:
43	chr19:42377016..42377922-chr19:42438274..42439260,2	K562	blood:
44	chr19:42375717..42378779-chr19:42460823..42464081,5	MCF-7	breast:
45	chr19:42376980..42377675-chr19:42438677..42439657,3	MCF-7	breast:
46	chr19:42373255..42375761-chr19:42417935..42419997,2	K562	blood:
47	chr19:42356783..42358615-chr19:42370430..42372693,2	K562	blood:
48	chr19:42376370..42377844-chr19:42455348..42456066,5	K562	blood:
49	chr19:42371951..42373649-chr19:42373763..42375308,2	MCF-7	breast:
50	chr19:42375846..42378575-chr19:42437686..42441355,5	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6797-5p	chr19:42373702-42373726	MIMAT0027494
hsa-miR-6797-3p	chr19:42373745-42373766	MIMAT0027495

No data

Variant related genes	Relation type
CD79A	TF binding region
ENSG00000142025	chromatin interactions
ENSG00000105404	chromatin interactions
ENSG00000268041	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000076928	chromatin interactions
ENSG00000105737	chromatin interactions
ENSG00000183103	chromatin interactions
ENSG00000170956	chromatin interactions
ENSG00000105369	chromatin interactions

Extended variants
information (count: 425 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531946233	chr19:42370562-42370563	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs550258961	chr19:42370572-42370573	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs367620211	chr19:42370577-42370578	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs554298310	chr19:42370584-42370585	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs77298848	chr19:42370600-42370601	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs61761239	chr19:42370608-42370609	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs61761240	chr19:42370664-42370665	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs367930726	chr19:42370676-42370677	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs370682975	chr19:42370721-42370722	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs146068423	chr19:42370768-42370769	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs538654654	chr19:42370769-42370770	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs35985786	chr19:42370811-42370812	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs61761241	chr19:42370850-42370851	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs149749137	chr19:42370863-42370864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs369737701	chr19:42370869-42370870	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs575302817	chr19:42370903-42370904	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs543960186	chr19:42370948-42370949	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs564103144	chr19:42370956-42370957	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs11879132	chr19:42370967-42370968	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs575788809	chr19:42371017-42371018	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs543250764	chr19:42371044-42371045	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs564868283	chr19:42371069-42371070	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs558225984	chr19:42371094-42371095	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs576896683	chr19:42371105-42371106	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs532933380	chr19:42371118-42371119	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs540652913	chr19:42371146-42371147	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs559266373	chr19:42371155-42371156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs529678945	chr19:42371157-42371158	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs543296235	chr19:42371170-42371171	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs77080563	chr19:42371174-42371175	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs559526197	chr19:42371187-42371188	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs553511862	chr19:42371243-42371244	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs571721435	chr19:42371275-42371276	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs539276346	chr19:42371280-42371281	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs184633301	chr19:42371294-42371295	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs531931695	chr19:42371302-42371303	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs113748599	chr19:42371337-42371338	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs76323565	chr19:42371338-42371339	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs560370791	chr19:42371397-42371398	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs71358996	chr19:42371439-42371440	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs572955999	chr19:42371503-42371504	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs550444746	chr19:42371512-42371513	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs112639563	chr19:42371516-42371517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs12984383	chr19:42371522-42371523	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs371341789	chr19:42371523-42371524	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs202166438	chr19:42371648-42371649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs547591376	chr19:42371678-42371679	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs540204525	chr19:42371753-42371754	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs566039789	chr19:42371776-42371777	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs113581314	chr19:42371793-42371794	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42365400-42374800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr19:42365400-42375000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr19:42365400-42376200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:42365400-42376600	Genic enhancers	Primary B cells from peripheral blood	blood
5	chr19:42365600-42370800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr19:42365600-42374600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr19:42365600-42374800	Genic enhancers	Primary T cells fromperipheralblood	blood
8	chr19:42365800-42370800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr19:42365800-42374600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr19:42365800-42374800	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr19:42365800-42375000	Genic enhancers	Fetal Intestine Small	intestine
12	chr19:42366000-42370800	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr19:42366000-42374800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
14	chr19:42366000-42376000	Strong transcription	HSMMtube	muscle
15	chr19:42366200-42371000	Genic enhancers	Colonic Mucosa	Colon
16	chr19:42366400-42377600	Strong transcription	Fetal Brain Female	brain
17	chr19:42366600-42374400	Strong transcription	Thymus	Thymus
18	chr19:42366600-42375000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr19:42366800-42370800	Genic enhancers	HMEC	breast
20	chr19:42366800-42374800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr19:42367000-42370800	Strong transcription	Fetal Lung	lung
22	chr19:42367000-42370800	Strong transcription	Rectal Smooth Muscle	rectum
23	chr19:42367000-42372000	Genic enhancers	Duodenum Mucosa	Duodenum
24	chr19:42367000-42373800	Weak transcription	Right Atrium	heart
25	chr19:42367000-42376600	Strong transcription	H9 Cell Line	embryonic stem cell
26	chr19:42367000-42376800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:42367200-42371000	Strong transcription	Brain Substantia Nigra	brain
28	chr19:42367200-42377200	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr19:42367400-42370800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr19:42367400-42371600	Strong transcription	Fetal Intestine Large	intestine
31	chr19:42367400-42372600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr19:42367400-42375600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:42367600-42370600	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr19:42367600-42370800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:42367600-42371400	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr19:42367600-42372400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr19:42367600-42374800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:42367600-42374800	Genic enhancers	HepG2	liver
39	chr19:42367600-42375200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
40	chr19:42367600-42375600	Strong transcription	Right Ventricle	heart
41	chr19:42367600-42376200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr19:42367600-42379200	Weak transcription	Fetal Brain Male	brain
43	chr19:42367800-42370600	Strong transcription	Brain Hippocampus Middle	brain
44	chr19:42367800-42370800	Strong transcription	Esophagus	oesophagus
45	chr19:42367800-42371000	Strong transcription	Adipose Nuclei	Adipose
46	chr19:42367800-42373400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr19:42367800-42374400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr19:42367800-42374800	Strong transcription	Brain Anterior Caudate	brain
49	chr19:42367800-42375800	Strong transcription	Left Ventricle	heart
50	chr19:42367800-42376200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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