EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS102-18666 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr5:141224600-141226180 
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
TTATTGAGCC CTTACAATAT ACCATGCTAA GCAACTTACG TGCATTCTCA CCTTAAATCC 60
ACACTGCATT TTTGGAATGT ATTATCCTCA TCTCATAGTT AGAAAAAGTG ATGCACAGAG 120
AGGTTAAGTA ACTTGTCTGA GACAGTCAGC CCGTCCAGCT CCAGACCAAA CTCACACACA 180
CACACACACC CTGACCTGTG TGGGTATGTG GAGGGGAGTC GTGCCAGGCC AGCGTCCACC 240
CTACTCTCTC TTTCTCCCCA AAGACAGGGC TCCTTTCAGT ATAATCCCCT CCCCCTGCTC 300
CTCCTCCACT CACCAGTGGA TTGGCCTAGA TTAGCAATCC TATATCCTTT ATCTGTTCCA 360
TACACAAATA TTGGTGGCCA GAGGTCAGGA GACTCCCAGG AAGGGGAGAA AGGAAGGTGA 420
GGAGCTAGAC AGGGTGACCA GGAGAGAGTG AGAGTGAGAG CTAGAGCTAG AGACAGAGAT 480
ACATGGAGAC AGACGAGAAG GGGCAGAGTA AAAAGCAAGT GGGCGTGAAG GGGTGCTAGT 540
GGCAGCTGGG AGGCTGTTAG AGAGACCCAT CAGCCTGTAT AGTCACAGCC CACCCCATCC 600
ACTGGGTGGC GATAGGATGG ATGGCAGGTG GTAGAAGGAA CTCCCACCCC CACCTTCACC 660
CAGCTTTGTC TCCACCCACC CTCCCCCTTC ACACCCCTGC TTCTCCTTCC CCTCCCCGAC 720
TGTCTTCTCC GGAACAATTC TGATTAGACT AAGTGACTAA GAGGTGGTTT CGGCCCGAAC 780
AGCCAATTAG GCCAGGAAGA AGAGAAAGTA GCTTCCCCAA GTCTTCCACC CCTACCCACC 840
CACCCCCATC TGCCTTTTTC ACCTAGACCA AGTATTCCTA TCCCAAGACT ACAGACTGTC 900
AAGAAAGTTC CCTTGATTCT GCCCACTCCT TACTGCCCAC TGTGCCCCGT TACCTGTGTC 960
CAGACAGCCC CTAATCTACT GCTTAGTCCC CACCCTGAGC TCCTCCGTCC TCAGGGCCCG 1020
AATCCACTCA CGTCTTCCTG GCAGGGTTGT AAGGAAAGGG TAGGGCTCTC CTTGGGAGGT 1080
TATCTTTCTA AGTCTCTTTA TTTCTCTTTC TCCCTTCTCC CTCTCCCTCT CTCTCTCCTC 1140
TTCCTCTGGC ACTTATTTCT AACATCCGTG GACCAGGCCT ACTGGTTGCC ATGGAGACGC 1200
ACGGTGCAGC TGGATGGTGA GTGTGTGTGA GAGGAGCTGT GTGCGCTCTG CAGCAGGGGC 1260
GGGCGGCTGT GTGTGAAATG TATCCATGTT ACAGGAAGCA TTCTTTGAGG GGGAATCAGA 1320
CAGGGATCCA GGCCGCCTCC TTGAAGTGAG ACCCAGGCCA AGGGGGAAAC TCTAAAAGGC 1380
CTAAGCCCCT AAACCCCTTG GTCATCTTCA TCTGGGAAAC ATCCACCCCT TGGCCCCTGC 1440
AGGTCAGATA CTAAATTCTG TTTCATCCAG GATCTGTAAT GGCAGATTCT GGAGGGGCCC 1500
TAACCTGCCC CGCCTGCCCA AGAGGACTAG GAACCCCAGA ACCCACTGGG AAAATAGCGG 1560
GCTGAGACCT GTCCTGAAAC 1580