EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS037-31666 
Organism
Homo sapiens 
Tissue/cell
ESC 
Coordinate
chr5:141224720-141226100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs57450513chr5141225446hg19
TF binding sites/motifs
Number: 14             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr5:141225783-141225799GGTTGCCATGGAGACG+6.38
RFX1MA0509.2chr5:141225783-141225799GGTTGCCATGGAGACG-6.4
RFX2MA0600.2chr5:141225783-141225799GGTTGCCATGGAGACG-6.55
RFX2MA0600.2chr5:141225783-141225799GGTTGCCATGGAGACG+6.77
RFX5MA0510.2chr5:141225783-141225799GGTTGCCATGGAGACG-6.26
RFX5MA0510.2chr5:141225783-141225799GGTTGCCATGGAGACG+6.27
RREB1MA0073.1chr5:141225428-141225448CCCCTACCCACCCACCCCCA+7.59
ZNF263MA0528.1chr5:141225723-141225744TCCCTCTCTCTCTCCTCTTCC-6.55
ZNF263MA0528.1chr5:141225726-141225747CTCTCTCTCTCCTCTTCCTCT-6.59
ZNF263MA0528.1chr5:141225720-141225741CTCTCCCTCTCTCTCTCCTCT-6.68
ZNF263MA0528.1chr5:141225708-141225729TCTCCCTTCTCCCTCTCCCTC-6.86
ZNF263MA0528.1chr5:141224889-141224910TCCCCCTGCTCCTCCTCCACT-7.16
ZNF263MA0528.1chr5:141224883-141224904ATCCCCTCCCCCTGCTCCTCC-7.39
ZNF263MA0528.1chr5:141224886-141224907CCCTCCCCCTGCTCCTCCTCC-9.07
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_03371chr5:141224218-141225289Brain_Angular_Gyrus
SE_03371chr5:141225439-141226228Brain_Angular_Gyrus
SE_03972chr5:141224421-141226481Brain_Anterior_Caudate
SE_05011chr5:141222204-141226586Brain_Cingulate_Gyrus
SE_05908chr5:141219577-141226644Brain_Hippocampus_Middle
SE_07007chr5:141224536-141226546Brain_Hippocampus_Middle_150
SE_07803chr5:141219691-141226608Brain_Inferior_Temporal_Lobe
SE_23100chr5:141224653-141225993Colon_Crypt_1
SE_24795chr5:141225468-141226051Colon_Crypt_3
SE_27969chr5:141224779-141225965Fetal_Intestine
SE_31440chr5:141219840-141226360Gastric
SE_32745chr5:141224728-141226088H1
SE_42262chr5:141219292-141226317Lung
SE_50145chr5:141219306-141225923Sigmoid_Colon
SE_52399chr5:141219312-141226230Small_Intestine
SE_65370chr5:141225153-141226472Pancreatic_islets
SE_68674chr5:141223569-141226501H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5141225430141226000
Number: 1             
IDChromosomeStartEnd
GH05I141837chr5141217507141226390
Enhancer Sequence
AGGTTAAGTA ACTTGTCTGA GACAGTCAGC CCGTCCAGCT CCAGACCAAA CTCACACACA 60
CACACACACC CTGACCTGTG TGGGTATGTG GAGGGGAGTC GTGCCAGGCC AGCGTCCACC 120
CTACTCTCTC TTTCTCCCCA AAGACAGGGC TCCTTTCAGT ATAATCCCCT CCCCCTGCTC 180
CTCCTCCACT CACCAGTGGA TTGGCCTAGA TTAGCAATCC TATATCCTTT ATCTGTTCCA 240
TACACAAATA TTGGTGGCCA GAGGTCAGGA GACTCCCAGG AAGGGGAGAA AGGAAGGTGA 300
GGAGCTAGAC AGGGTGACCA GGAGAGAGTG AGAGTGAGAG CTAGAGCTAG AGACAGAGAT 360
ACATGGAGAC AGACGAGAAG GGGCAGAGTA AAAAGCAAGT GGGCGTGAAG GGGTGCTAGT 420
GGCAGCTGGG AGGCTGTTAG AGAGACCCAT CAGCCTGTAT AGTCACAGCC CACCCCATCC 480
ACTGGGTGGC GATAGGATGG ATGGCAGGTG GTAGAAGGAA CTCCCACCCC CACCTTCACC 540
CAGCTTTGTC TCCACCCACC CTCCCCCTTC ACACCCCTGC TTCTCCTTCC CCTCCCCGAC 600
TGTCTTCTCC GGAACAATTC TGATTAGACT AAGTGACTAA GAGGTGGTTT CGGCCCGAAC 660
AGCCAATTAG GCCAGGAAGA AGAGAAAGTA GCTTCCCCAA GTCTTCCACC CCTACCCACC 720
CACCCCCATC TGCCTTTTTC ACCTAGACCA AGTATTCCTA TCCCAAGACT ACAGACTGTC 780
AAGAAAGTTC CCTTGATTCT GCCCACTCCT TACTGCCCAC TGTGCCCCGT TACCTGTGTC 840
CAGACAGCCC CTAATCTACT GCTTAGTCCC CACCCTGAGC TCCTCCGTCC TCAGGGCCCG 900
AATCCACTCA CGTCTTCCTG GCAGGGTTGT AAGGAAAGGG TAGGGCTCTC CTTGGGAGGT 960
TATCTTTCTA AGTCTCTTTA TTTCTCTTTC TCCCTTCTCC CTCTCCCTCT CTCTCTCCTC 1020
TTCCTCTGGC ACTTATTTCT AACATCCGTG GACCAGGCCT ACTGGTTGCC ATGGAGACGC 1080
ACGGTGCAGC TGGATGGTGA GTGTGTGTGA GAGGAGCTGT GTGCGCTCTG CAGCAGGGGC 1140
GGGCGGCTGT GTGTGAAATG TATCCATGTT ACAGGAAGCA TTCTTTGAGG GGGAATCAGA 1200
CAGGGATCCA GGCCGCCTCC TTGAAGTGAG ACCCAGGCCA AGGGGGAAAC TCTAAAAGGC 1260
CTAAGCCCCT AAACCCCTTG GTCATCTTCA TCTGGGAAAC ATCCACCCCT TGGCCCCTGC 1320
AGGTCAGATA CTAAATTCTG TTTCATCCAG GATCTGTAAT GGCAGATTCT GGAGGGGCCC 1380