EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-14575 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:50002970-50004040 
Target genes
Number: 43             
NameEnsembl ID
BAXENSG00000087088
FTLENSG00000087086
RUVBL2ENSG00000183207
SNRNP70ENSG00000104852
LIN7BENSG00000104863
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
PRR12ENSG00000126464
RRASENSG00000126458
SCAF1ENSG00000126461
BCL2L12ENSG00000126453
IRF3ENSG00000126456
PRMT1ENSG00000126457
C19orf76ENSG00000224420
CPT1CENSG00000169169
CTBENSG00000243829
U6ENSG00000206599
AP2A1ENSG00000196961
MED25ENSG00000104973
PNKPENSG00000039650
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZIC1MA0696.1chr19:50003290-50003304CCCCCCCTGCTGTG+6.09
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
chr195000320050003800
Enhancer Sequence
CTTTACCAGA GCATTGGTGG GGGTGGGGGT GTGCCTCGGG GAATTGGGCA GAGCTGCTGT 60
CAGAGAGGCT GCCTGCCCAT GTCTGTGGGT GAGGACAGTG GAGCCTGAAC TGAGATGCCT 120
GCCTTCCCCT GGGTCTCCTT CTTTGGTCCT TGTCACCTTT TCGGTGTCTG AATAAGGCTG 180
ATTACCTGGC GTTGCGCTGT CCCCCCGCCC CCTCCGGTCT CTGGGGAGGA AGTGAGTGAC 240
GGCGGAGGCC CCTGGGTCCT CCAGGCCCTG GTCTGTCTCT TTCCTGACCA CCTCGGGTGG 300
GGAGGGGAAG AAGCTGCAGC CCCCCCCTGC TGTGGGCATG GGCTCACCCA GGTAGAGTGG 360
GATGTGCTGA GGCCCTGTTG TCTGGCTGTG AAGTGTAAAG GTCTTGGCTT TAGCCTGGGC 420
CTCCTATCCC TCCTTACAGC CAAGGATGGG GGCCCCATGC ACGCACCACA CACGCCTAGT 480
TGGGCACCAG GCCTATCTGC AGATGAGGAA ACTCATCTGG GAGAGGCCAA GCCCTCCACC 540
TGAAGTCCCA GTGAGTAGCT GAGTTACAGG TCTCAGATTC TAGAAACTTC CTCTGCGCCA 600
GCTGCCTCAA AATCGCAGTA AGGAAATTGG TGGTGTGGGC AAGTGGCATC ATGAGGCTCC 660
CCTGGAGCCT GTTCAGTGGT ACCGGGGCCC AGGCTGCTGG GAAGGAAGTG GGCAGGAAGC 720
GTCCGGAGAC GGCCCAATAC ACACAGGCCG CAGAGATGGG GGCCTTGAGA GGAACAGGAC 780
AGGACACACG GTGGCCCAGG GTTGTGGCAC ATGGGGAGGA GGGGTTTTGC AGAGCTGGGG 840
AGAGCACAGA CCACCGCGAG AGGCAGGTAC AATAGAAACA GGTGTACTTT GCGCATCACA 900
CAGAGGTGGG GACGACAGGC ATGGGGTGGG GGCGGTGAGG CAGGAGCGCA CCAGAGGATA 960
TGTGGGACCC GAAGGGGAGA GACGCATAAA AGCCGCAGCA GAGATGGGAG TACAGGGAGG 1020
GGAGGTCCCA ATGCCCGCTC ACCTCACCCC TTGGGGCCTG CCGGTGCCGG 1070