EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-32885 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr5:141224470-141226000 
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
AGAGGCAATT TGGGCCCCCA AGAATGGAGA AGCAGTGGCA GGAGGAGGGG ATTGGAAGAT 60
GCAGCTGTCC TGGCTCCAGA AGGACCCCGG AGAAAGGACA AGAGTCTGGA GTGATGATAA 120
AAGCTGCCAT TTATTGAGCC CTTACAATAT ACCATGCTAA GCAACTTACG TGCATTCTCA 180
CCTTAAATCC ACACTGCATT TTTGGAATGT ATTATCCTCA TCTCATAGTT AGAAAAAGTG 240
ATGCACAGAG AGGTTAAGTA ACTTGTCTGA GACAGTCAGC CCGTCCAGCT CCAGACCAAA 300
CTCACACACA CACACACACC CTGACCTGTG TGGGTATGTG GAGGGGAGTC GTGCCAGGCC 360
AGCGTCCACC CTACTCTCTC TTTCTCCCCA AAGACAGGGC TCCTTTCAGT ATAATCCCCT 420
CCCCCTGCTC CTCCTCCACT CACCAGTGGA TTGGCCTAGA TTAGCAATCC TATATCCTTT 480
ATCTGTTCCA TACACAAATA TTGGTGGCCA GAGGTCAGGA GACTCCCAGG AAGGGGAGAA 540
AGGAAGGTGA GGAGCTAGAC AGGGTGACCA GGAGAGAGTG AGAGTGAGAG CTAGAGCTAG 600
AGACAGAGAT ACATGGAGAC AGACGAGAAG GGGCAGAGTA AAAAGCAAGT GGGCGTGAAG 660
GGGTGCTAGT GGCAGCTGGG AGGCTGTTAG AGAGACCCAT CAGCCTGTAT AGTCACAGCC 720
CACCCCATCC ACTGGGTGGC GATAGGATGG ATGGCAGGTG GTAGAAGGAA CTCCCACCCC 780
CACCTTCACC CAGCTTTGTC TCCACCCACC CTCCCCCTTC ACACCCCTGC TTCTCCTTCC 840
CCTCCCCGAC TGTCTTCTCC GGAACAATTC TGATTAGACT AAGTGACTAA GAGGTGGTTT 900
CGGCCCGAAC AGCCAATTAG GCCAGGAAGA AGAGAAAGTA GCTTCCCCAA GTCTTCCACC 960
CCTACCCACC CACCCCCATC TGCCTTTTTC ACCTAGACCA AGTATTCCTA TCCCAAGACT 1020
ACAGACTGTC AAGAAAGTTC CCTTGATTCT GCCCACTCCT TACTGCCCAC TGTGCCCCGT 1080
TACCTGTGTC CAGACAGCCC CTAATCTACT GCTTAGTCCC CACCCTGAGC TCCTCCGTCC 1140
TCAGGGCCCG AATCCACTCA CGTCTTCCTG GCAGGGTTGT AAGGAAAGGG TAGGGCTCTC 1200
CTTGGGAGGT TATCTTTCTA AGTCTCTTTA TTTCTCTTTC TCCCTTCTCC CTCTCCCTCT 1260
CTCTCTCCTC TTCCTCTGGC ACTTATTTCT AACATCCGTG GACCAGGCCT ACTGGTTGCC 1320
ATGGAGACGC ACGGTGCAGC TGGATGGTGA GTGTGTGTGA GAGGAGCTGT GTGCGCTCTG 1380
CAGCAGGGGC GGGCGGCTGT GTGTGAAATG TATCCATGTT ACAGGAAGCA TTCTTTGAGG 1440
GGGAATCAGA CAGGGATCCA GGCCGCCTCC TTGAAGTGAG ACCCAGGCCA AGGGGGAAAC 1500
TCTAAAAGGC CTAAGCCCCT AAACCCCTTG 1530