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

TagContent
EnhancerAtlas ID
HS098-31056 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr2:105877320-105878470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17636747chr2105877870hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFAT5MA0606.1chr2:105877856-105877866AATGGAAAAT-6.02
NFATC1MA0624.1chr2:105877856-105877866AATGGAAAAT-6.02
NFATC3MA0625.1chr2:105877856-105877866AATGGAAAAT-6.02
NKX2-3MA0672.1chr2:105878271-105878281ACCACTTGAA+6.02
Nr2f6(var.2)MA0728.1chr2:105877992-105878007AAGGTCAGGAGTTCA+6.04
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2105877677105877808
Number: 1             
IDChromosomeStartEnd
GH02I105260chr2105877161105878721
Enhancer Sequence
TTTGGGGAGG GCATAAAATT TGAGTTTCTG ACTATGTTTA CTCATATAAA GGGAATACAT 60
TCTTGTAAAC TGACTGAAGT CAAAGAAACT GAATCTCTTT TGAGGTGTAC ATCATTATGT 120
CTTGTAAACA ACTGAGAAAT GCTCTCCTGT ACTCTGTGTT AAGAAAGTAA GTTTAGGATT 180
TCAGTTATAT TCGTTTATAA GCTTCAGTCA ATAGCTGCCT GTAAGTCAGC AACATATTAA 240
AAAACAGTTT GGAAATAGTT GGTGGGGTTT TACCATAATG TGCTGGCTGC AGAGGCGGGA 300
GTGAGGGAGG GTAGGCCAAC TGACCACCCC AGTTCTATCA TGCACATTGC TGTGGAGGTA 360
AATCATAAAC ATGTGTGGGC AACCAGACAG AGGCAGGGGC TGGGTGAGTC AGCTCAAAGC 420
ACGTAGCGTC ATCTTAGCTC ACATTCCTGT TGAGGTCAGG TTGGGGATTG GCCACCCCAG 480
CTTCGTTGCA CACACATGGA TTCCGAAAGG GAAAAACTGA TATTTCAAGC AAGACAAATG 540
GAAAATGTTC TCTAGAGAAA GAGGAAGGAC TTGTGAAACC TAGAGCACAT GAGAAAAGGC 600
AAGGGGAGCC GGGCACAGTG GCTCAAGCCT GTAATCTCAG CACTTTGGGA GGCCGAGGTA 660
GGAGGATCAC TTAAGGTCAG GAGTTCAAGA CCAACCTGGC CAACATAGTG AAACCCTATC 720
TCTACTAAAA ATACAAAAAT TAGCTGGGCA TGATGGCATG TACCAGTAGT CCCAGCTACT 780
CGGGAGGCTG AGGCAGGAGA ATCGCTTGAA CCCGGGAGGT AGAAGTCACA GTGAGCCGAG 840
ATCACGCCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAC TCCATCTCAA AAAAGGACAG 900
GACAGGCAAG GCAAGGCAAG GCAGAGGCTG GAGGAAAAGG GGCAACTGAA AACCACTTGA 960
AAAAAGGTAT GTGTAGACCA ACTCCTCTCC TGGGTCCAGC TGGAACCGGG ATTGAGGAGT 1020
AGAGTGGGCT AGAGTCACTT TCCAAATCAA GGAACCATGC AATGAGATTC CGGAGTGCTC 1080
AGACACACCT GTGGGGGCAC ATCTGTGGGA TGTGTGCATG AGTCCCTGTG CTGGGTGCTT 1140
TCAAGGGCCA 1150