EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-20893 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr2:47229610-47232100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17540621chr247229839hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr2:47231406-47231420GTGAGTCACTTCCT-6.15
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.94
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.95
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.77
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.83
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.14
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.27
RORA(var.2)MA0072.1chr2:47230175-47230189CTGACCTAATTAAC-6.05
ZNF263MA0528.1chr2:47231802-47231823GAATGAGCAGGAGAAGGGAGG+6.27
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00056chr2:47228729-47233257Adipose_Nuclei
SE_00864chr2:47228939-47232656Adrenal_Gland
SE_01547chr2:47229049-47237427Aorta
SE_03148chr2:47228934-47232779Brain_Angular_Gyrus
SE_03864chr2:47224295-47237133Brain_Anterior_Caudate
SE_04790chr2:47207331-47238050Brain_Cingulate_Gyrus
SE_05773chr2:47203345-47237435Brain_Hippocampus_Middle
SE_06717chr2:47224482-47237491Brain_Hippocampus_Middle_150
SE_07731chr2:47224149-47237360Brain_Inferior_Temporal_Lobe
SE_08824chr2:47229662-47231117Brain_Mid_Frontal_Lobe
SE_08824chr2:47231233-47231571Brain_Mid_Frontal_Lobe
SE_09141chr2:47226225-47233894CD14
SE_26122chr2:47229467-47230939Duodenum_Smooth_Muscle
SE_26616chr2:47229058-47231804Esophagus
SE_26616chr2:47231831-47232707Esophagus
SE_48626chr2:47229031-47231103Right_Atrium
SE_53323chr2:47229516-47230518Spleen
SE_54495chr2:47226285-47245145Stomach_Smooth_Muscle
SE_65882chr2:47229163-47232588Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24723098247231623
Number: 2             
IDChromosomeStartEnd
GH02I047001chr24722903247231739
GH02I047004chr24723183247232707
Enhancer Sequence
TCTGAGGCCA CTTCAATGGT GGAAGGGAAA GAGTGTGGCT GGGACTAGGT CAGAGCTACT 60
CCCAGAGCAT GGGGGTACAC CATGTGGCCT GAGGGCAGTG AGCCAGGGAG GAGGGAGCAG 120
GACAGCTGGG GGTGCTGGGA AGGAACTGAT GCTCCCATAG TGTCTGAGGC CCTGGCCTCA 180
GAGGCTAGCC CTGGCCCCTG AGCTGCACAT TAATTCTGTT CTGCTGTGGC TTACCCACCA 240
GCCCCCATGC CTGCCTTTTC TCTGTCCCAT TTCCCCCTAC CCCTCCCTGT TGCCATGGTT 300
ACACACACAG GCACTGCCCA GCAACCACCA GGAATATTTC ACTTCGGCCC TGCCCCAAAG 360
CCATAGTAAC CACTCAGCCC ACTTCTGCTT CTGGCTGGGG AATCACAGCC CTCTCTTGCA 420
CAGGCCCCAG TTCGCACCAG TCCCTAGGAC CCCCAGGGAG CCTTCCTGGC TGCCTGCCTA 480
TTGAGGGCCT ATCACCAGCC TGAGGATTTG TGCTGCTGCT GCTGCCGCTG CTGCTAGTAT 540
GCTCCTCTCT TCTGTTCCTA TTCTTCTGAC CTAATTAACG CCCGGTTCTG AAAATCCACC 600
CCTCCCTCTG CCAGACACAA ATTCAGACAC TGTTCTCTTA AAGGTCAAGG TCTAGGGTGG 660
ACAGGGGGAG GTTTCCACTC CAGGCCCAGA GTCTTTCTCT CCTGAGTGTC ACACCCTGCA 720
GGTTGAGTCA AGTTCTGTGC GTGAGGCTGT GCCTGGGGCC AGGAGTCTAG CCATGAGCAA 780
GAACTGGTGA ACCAGACGGG GGCATGTGAG CTGAGGCATG GGCTGGGTTG GGGGAGGACA 840
GGAGAGGCCT GACCTCTCCT GGTGAGATGA GTTAGGGATG GTGCTGTAAG AGGGTGGTCC 900
TGAATGGGGT TGTGAGGAGG TAGAAGGTGT CCAGGTTGAT AGAGGGAACT GCAGCATGAC 960
CGAAGATGGG CCATGGTGAC TGTAGGGACC AGCAAGGGGT TCCATGTCAC TGGAGAGAAG 1020
CCCGCCAGTT AGGCTGCCCC AGAAAGGAGT TTAGATTTTA TCCTGATGGC CATAGTGATG 1080
GCTCGCAGCC CACTATCCCC TGAACAAGAT TGGTCTGCAC AGACAGGCAG GAGGGTCCCC 1140
AGACCCTGGA TGTGCCCAGC CAAGCTTCTT CCCACCCCTG CAGACTGCCT GGCTCCACCC 1200
GCTCCCATCA TAACCTCTTG CTTCCACCAG AATTCCAGGT CAGCCTCCAC TCGGGGATGT 1260
GCATCCTATA ATGCTGCTCC TTCCTGTTCT CCCCATGGGC AGGGCCTCTG TGCCCCCGTC 1320
CTCTCACACC CGAGCCACTC TTGCCTGTTG GAGGCCGCCC CTGTGGGTCC CCACCCTGGG 1380
TGGCCAGAGC TGGGGAGCTG CTGGAGGTGG TGGAGTGGGT CAGTACATCG CCGGGGACAG 1440
AACGAGGGCT GTATTCCTAG TTGGCTCAGG GGACTAGCTC CTGCCAACCC TCTCCCTAGA 1500
ATTTCTTCTC TCTTCCTGTT GGTGGCTGTG TGGGTGGACT TCACTGGGAA GGAGGGGGAT 1560
TTCTTGGCAC CTTCTTTCTC CACTCCTCTC CTTCAACCCT TTGGAGCTCC TGAGTGGCTC 1620
CTGTTCCACA GGCTGACTCC AGAGCTCAGC CTTGCCGGGA TTTCCGGGCA TCCCGGCACC 1680
CTCTCCTGGG CCATCTAAGT CCATGGGGGC ATGGGCAGCA CTCACCAACT GTGGCAACAG 1740
GGCAGCCATC AGAACCCCTG GCCACCAGTC TCTCAGTGAC TGAGCTGTCC CCCAGGGTGA 1800
GTCACTTCCT TGGGTCTTGG AGGTGTTTTG GCTTCCAGAG GCTTCTGGGA GGACTCCCTC 1860
CAGCCCTGCG CTGCAGGACA CACCCAGAGC CTGTGGTCTG GAGGCCTCAG GGGCTTGGGC 1920
TTCTGCCTCC AGCGCCTCAC CTGGAGGAGG GGAGAGCAGT CCTGCCCAAG GGAAGCTGTG 1980
AGGCCCACTT GCTGCATAGG AGGGATGGGG TAGCTCTGAT GAGGGAGATC TGGGTTTTTA 2040
GGGCTGGCAG CTCCTTTTTA TTCGGTTAGG AAGGCTGAGT CCTTGGTCTT GAGGTCCTGT 2100
GTATGGAAGC AGAGGAGGGC AAGTACTATT GTACAGAAGG AGGCTCAGAC AGAGGGAGGG 2160
AGATGCAGGA GAGAGCCCCA TTTGGCAGAG GGGAATGAGC AGGAGAAGGG AGGATGCTGG 2220
GGGCGGCCCC CAGCAGCATC TGCCCAGAAC ACAGCTCTGC CCAGCTCCCG CACAGCCCTT 2280
GGAGTGGGGG TGGATATGTT ACCATTTCTG GCCCCAGAGT GTCCTCTGCC TAAGTCCCTG 2340
CCCTGTGGCT GCTTGGAGGC CCCCATGACT CCTGCAGCTG AGGAGCTTCT CCCTTTCCAC 2400
CTTTTGCCCC CAGCCTGCGT GTTGCCCCCA GGGTATAGAG GTGGGCAGAG GGGTGGGACT 2460
ATCTGCACAT ACCAAAGAAC ACAAGAGTCC 2490