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

TagContent
EnhancerAtlas ID
HS050-30228 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr17:76404440-76406070 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4969143chr1776405736hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TCF3MA0522.2chr17:76405422-76405432AGCAGGTGTT-6.02
ZBTB18MA0698.1chr17:76404983-76404996ACACATCTGGATG-6.78
ZNF263MA0528.1chr17:76405178-76405199CTCTCTTCATCTTTCTGCTCC-6
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00336chr17:76403376-76405707Adipose_Nuclei
SE_09402chr17:76402394-76405762CD14
SE_18476chr17:76402170-76405866CD4p_CD25-_Il17-_PMAstim_Th
SE_24583chr17:76404346-76406027Colon_Crypt_2
SE_26825chr17:76404693-76406004Esophagus
SE_31461chr17:76404354-76405962Gastric
SE_36965chr17:76401030-76406003HSMMtube
SE_42104chr17:76404335-76406043Lung
SE_50905chr17:76402998-76406411Sigmoid_Colon
SE_51088chr17:76403004-76406193Skeletal_Muscle
SE_53161chr17:76403031-76406409Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177640532976405828
Number: 1             
IDChromosomeStartEnd
GH17I078406chr177640281476406178
Enhancer Sequence
TTTACCTGTG GCCACAGCTG AGGGGCCTGG CTTAACCTCT TTCCTGTGCA GTCGGGGGGA 60
TGGCTCTAGA TTGTCAGGAG GACACGGGGA ACAGGGCTGA TATTTGACTT TCTATAAAAT 120
AACCGTATGG TTCCTAGGCC AGGTGAGGCA CCTTGGTGGG GCGCGTGGAG GTTGAAATCA 180
CACTGGGGGC CGAGGGCTGC TGCGCGTCCC TGAGCGAATA GATTGGCAGA AGGGAGTGGG 240
GTGGGGGCCT TGGATCCCTT GGTGCCGTGT CTCTGGCCTT GCTCCCTGTA GTTCTGTTGC 300
GCTGATTCGG TCGTGAAGGA AGGTGCTGCC AGGCCGCTTC ACCTGCATCG CCTTGGCTTT 360
GGGAGGTGGG GCTGAGTGGG CATCTGGGTT GGATCTCAGG CAGGTGGCAG TTCCTCTGAT 420
TCATGGTTGT CAGTTTCCTG TTGCCTGGCC CTCGCTCCTC GCCCAGTAGG TGTGGTGGGA 480
CAAGGTTCTG GGAGCTGGGG TAGAATTTGG ACTCTTAACG GGAAGTGCCT CGTGCTGCCG 540
CAGACACATC TGGATGGGTG CTGAGCTTTC CTTCCCAAGC CTGGTCCTGA TCGGGGGTGG 600
GGTACAGGCA GGAGCAGCCC GGCCTTGTCA GCCGTTGAAA GTGTGGTATC TGCTGGGTTG 660
CCAGTAAGCT CGCTTCGAGG TCTTGAGAGG CAGTGCAGGG GAGGCTGAGT ATGAACCGTG 720
TCAAGCCAGT TCTTATGTCT CTCTTCATCT TTCTGCTCCA TGGAGGTGAG GGACAGAGTG 780
AGTGGTGCCC ATCCCATTAT CACATTCAGG CAGGAACCAT GCTGTGCTGA GCCAGGCTGT 840
GTCCATCTGC TGGGACATGG GCTCTGCCCT CCGGCGTGCA TTTCATGAGG AAGATCAGAA 900
AGTGAGTTTT AGCATGTTGA CTTCCATTTC TTCTGGACGC AGTATTCTAG CACTAACAAC 960
ACAATGTGGG TGGCTAGGGC GGAGCAGGTG TTGGATTAAG AGATTTCTGG CTCATGCTGA 1020
CAGGGAAATC TGTTAATGGT TGTGAGAATG TCACTATTTT TATTGCCTTC CTGATAGGCC 1080
AATTGGCGTT CTGCCCAAAG GTGAACTGAT GGTGAGAGGC GGGCAGCCCC ACCCTGTTTG 1140
CCTAGGCCAC ACGTGAGGCG GCTCTCCCCT GGGCACCCAG TGGGTGTGGT AGGGGTGCTG 1200
TGCCCGTGCA AATTGCTTGC TTCAGGCTGA GCACACACAC CAGCCTGTGG GCCCTTACAG 1260
TTTCTCAGAG CTGTACTAAT GTCAGAGCAG GTGAGTGCTT ATCCTGTAAG GATAAGCCTG 1320
TGATGTCTTC TGTCCCCTCC GTGTTTTTAC TGGAGTCTGA GAACCCTGTA AGATTTATTG 1380
CAGAATACTG TGGGAGTGCT TGAGGGAGGA GTATGTGTTC ATGCATGTAC TCTTAAAATG 1440
TTCATACACT TCTGCCTTAG AACTGCAAAG GCCTGGCGTG GTGGCTCACA CCTATAATCC 1500
CAGCACTTTG GGAGGCCAAG GTAGGCGGAT CACCTGAGGC CAGAAGTTTG AGACCAATCT 1560
GGCCAACATA GTGAAACTGT GTCTCTACTA AAAATACAAA AATTAGCCGG GTGTGGTGGT 1620
GCATGTCTGT 1630