EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS051-14574 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:50001300-50002760 
Target genes
Number: 45             
NameEnsembl ID
NTF4ENSG00000167744
SNRNP70ENSG00000104852
AC011450.2ENSG00000235555
SLC6A16ENSG00000063127
CD37ENSG00000104894
AC011450.1ENSG00000197813
TEAD2ENSG00000074219
DKKL1ENSG00000104901
CCDC155ENSG00000161609
PTH2ENSG00000142538
CTDENSG00000261949
SLC17A7ENSG00000104888
PIH1D1ENSG00000104872
ALDH16A1ENSG00000161618
FLT3LGENSG00000090554
RPL13AENSG00000142541
SNORD32AENSG00000201675
SNORD33ENSG00000199631
SNORD34ENSG00000202503
SNORD35AENSG00000200259
RPS11ENSG00000142534
SNORD35BENSG00000200530
MIR150ENSG00000207782
FCGRTENSG00000104870
RCN3ENSG00000142552
YENSG00000207073
NOSIPENSG00000142546
PRRG2ENSG00000126460
PRR12ENSG00000126464
RRASENSG00000126458
SCAF1ENSG00000126461
BCL2L12ENSG00000126453
IRF3ENSG00000126456
PRMT1ENSG00000126457
C19orf76ENSG00000224420
CPT1CENSG00000169169
CTBENSG00000243829
U6ENSG00000206599
AP2A1ENSG00000196961
FUZENSG00000010361
MED25ENSG00000104973
PNKPENSG00000039650
TBC1D17ENSG00000104946
ATF5ENSG00000169136
NUP62ENSG00000213024
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2009984chr1950001877hg19
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_14855chr19:49998586-50006523CD4_Memory_Primary_7pool
SE_15707chr19:49998891-50005390CD4_Memory_Primary_8pool
SE_16751chr19:49998964-50005509CD4_Naive_Primary_8pool
SE_20689chr19:49998708-50006423CD56
SE_21347chr19:49998834-50005646CD8_Memory_7pool
SE_21688chr19:49998862-50005732CD8_Naive_7pool
SE_22993chr19:49998692-50006351CD8_primiary
SE_68187chr19:49976788-50037595TC32
SE_68188chr19:49976788-50037595TC32
SE_68189chr19:49976788-50037595TC32
SE_68190chr19:49976788-50037595TC32
SE_68191chr19:49976788-50037595TC32
SE_68192chr19:49976788-50037595TC32
SE_68193chr19:49976788-50037595TC32
SE_68194chr19:49976788-50037595TC32
SE_68464chr19:49990162-50019336TC71
SE_68465chr19:49990162-50019336TC71
SE_68466chr19:49990162-50019336TC71
SE_68467chr19:49990162-50019336TC71
SE_68468chr19:49990162-50019336TC71
SE_68469chr19:49990162-50019336TC71
SE_68470chr19:49990162-50019336TC71
SE_68471chr19:49990162-50019336TC71
SE_68472chr19:49990162-50019336TC71
SE_68473chr19:49990162-50019336TC71
SE_68474chr19:49990162-50019336TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr195000136850001601
Enhancer Sequence
CAGGTGAGCG CAGTGGCCCA TCAGGTTGCT CAGGCCACGC TCTCTCAGCC TTCAGATTCC 60
AGATCGGACC AATTTAAGGC CAACTGAGGG AGGGAAAGAC TGAGGTGGCA TCTCTGGGAA 120
GCCCCAGAAT CTCAGGATTT GTATATCATA TGTTCTTCAG AATCAAAGCG TTCTACAGGG 180
TGAATATCTC TACCTGAAAT GCTTGGAACC AGATTTTGGA ATGTTCTCGC ATACATAGTG 240
AGATGTTTTG GGGATGTGAC ATAGGTCTAA ACAAGAAGCT CATTTGTTTC ATATACACCT 300
TATTCACATA GCCTGAAAGT AGTCTTACGC AGTGCGTTTT ATAATTCTGT GTGAAACAAA 360
GTTTGCGTAC ATTGAACCAT TGGAAAGCAA AGGTGTCACG CTGGTATTGA AGAAGTTTCA 420
GATTCTAGCC AGGCACCGTG GCTCAAGCCA GTAATCCCAG CACTGTAGGA GGCTGAGGCA 480
GGAGGATCCC TTGAGCCCAG GAGTTTGAGA CCAGCCTGGG CAACATGGCA AAACCCTCTC 540
TCTACAAAAA ATACAAGTTT GCCAGGTGTG GTAGCATGTG CCTGTAGTCT CAGGTCTTCA 600
GGCGGCTGGG GTGGGAGGAT TGCTTGAGCC CAGAAAGTGG AGGCTGCAGT GAGCCGAGAT 660
GGCAGCACTG CTCTCCGGCC TGGGCGACAG AGTAAGACCC TGTCTCTCCC ACACACACAC 720
AAATTCAGAT TTTGCAGCGT TTCAGAATTT TTGGATTAGG GTGCTGAACC TGTAATAGGC 780
AGGTGCGTTT GAACCAAAAG GTTAGGATGT CATACCAGAT GGGAACCTCA GAAATGTTGG 840
AATTAAACGT TTGTTCATTC CCTCAGCATG TTTTAGTTAG AGCTTATCAC GTACCAGGTG 900
TGGTGTGAGA TGTTTGGGGT TCAGTGGTGA GCCAGGAACA AAGTCCTGCT CCCTCAGAGG 960
GCACCTTCAA GCAGTGTGGG TGCCAGATGA CAGCCAAGTA TAACCAGAAT GGGGATGTGG 1020
GCAGCTGATA TTGGTGGCCC TCTGGGCGGG GAGGATCTTG GGAGCAAGGT GAGGAGTCCT 1080
GTGGGTGGAG AGGAGGGTGG CCCAAACTGA TGCTGAGCGA TAAGGGACCT GTGGTTGTCA 1140
GTGCTGCAGG ATCCCCCTGC TGCTCTGCTG GGGAAGGGTG GTGAGGCTGC TGACAACTTG 1200
GGGGCCTCCA GTTTGCTTGT GAAATGGAGC TCGTCCACCC CAGCGGTCCT CGGAGGGGTG 1260
GTGGCCTGCT CTGTGTACAG CGTTGAGCTT GGTGCTTGGC ACAAAACTTG TACGAAAGGA 1320
GGGGACAGGT TGAATTGGCG AGTAGAGCTT GGTTGGGGTT TGGTGGAGCC GAAGCAGAGA 1380
GCCTTTAGCC TGGTGAAGGG GAGGGAGGGC CTCCTGGGGT CTGCTGGGGT GGCCCCTCCT 1440
GAGGACATGG CCCTACCTGC 1460