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

TagContent
EnhancerAtlas ID
HS040-00489 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr1:12244450-12246470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs474247chr112246175hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:12245361-12245382TTTTTCTTTTTCTTTCTCTTT+6.77
ZNF263MA0528.1chr1:12245259-12245280CCCCTCCGCCACCCCTCCCCC-6.22
ZNF263MA0528.1chr1:12246380-12246401TGAGGAAGGGGAGGAGGAGGC+6.78
Znf423MA0116.1chr1:12245459-12245474GCACCCCTGGGTGCT-6.35
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00369chr1:12226565-12247198Adipose_Nuclei
SE_01471chr1:12243922-12246504Adrenal_Gland
SE_04546chr1:12243735-12246962Brain_Anterior_Caudate
SE_06521chr1:12243738-12246994Brain_Hippocampus_Middle
SE_09154chr1:12224797-12249846CD14
SE_10696chr1:12243928-12245111CD19_Primary
SE_14553chr1:12243811-12245422CD4_Memory_Primary_7pool
SE_14553chr1:12245589-12247318CD4_Memory_Primary_7pool
SE_17827chr1:12231021-12246713CD4p_CD25-_CD45ROp_Memory
SE_18389chr1:12226183-12250288CD4p_CD25-_Il17-_PMAstim_Th
SE_19117chr1:12243746-12249924CD4p_CD25-_Il17p_PMAstim_Th17
SE_20048chr1:12243749-12245373CD56
SE_20873chr1:12243794-12244892CD8_Memory_7pool
SE_22347chr1:12243335-12245917CD8_primiary
SE_26251chr1:12243680-12246989Duodenum_Smooth_Muscle
SE_27503chr1:12243903-12246642Esophagus
SE_30788chr1:12243698-12246708Fetal_Muscle
SE_32030chr1:12243891-12246634Gastric
SE_38661chr1:12243533-12246545HUVEC
SE_41498chr1:12243811-12247059Left_Ventricle
SE_42336chr1:12243813-12247305Lung
SE_48967chr1:12243799-12246749Right_Atrium
SE_50250chr1:12243815-12247081Sigmoid_Colon
SE_52522chr1:12243745-12249859Small_Intestine
SE_53313chr1:12243756-12247385Spleen
SE_55394chr1:12244622-12245112Thymus
SE_61096chr1:12184746-12245090HBL1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11224534812245387
Number: 1             
IDChromosomeStartEnd
GH01I012182chr11224245912247879
Enhancer Sequence
CAAGGGAGCC GACCCCCTCT GCCAGCTACT GGGGGCTGGA GGCTCACAGA GCCAGGGAGG 60
AAGTCCTACC CCCTCTGCCG GCTACCGGGG GGGCTGGAGC CACACAGAGC CAGGGAGGAA 120
GTCCAGGGAC GGTCACTCAC AGCAAAGCCT CAGACAAGAG AGGAACCTGG AGGGGAGGAG 180
GTGGGAGGCC ACCACTCAGC CGGCCTGGGG GCCATGGGAG TCCAGCTGCC TGCCGTTAGT 240
GGCCAGGAGC CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA ACTTGGCCAC GGCAGGGCTC 300
TTTCCCATCA GGCCCTTTGA GCCCTGATGG GAAACCCTTC CCCAGCCAGG GTGGGATTTC 360
TTGCTGCCGC CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG GCCCTGGAGG AGTGAGGGGC 420
TCCCCTGGTT ACCCCAAGGG CACTCGTGGG GATGAAGCCC GCGGGATGCA GGATTCCCAC 480
GAGACCTGTG CTGGCCACTG TGCGGGGTGG GGGGCTGCCA GGGAAGAGGT GCAGCCCCTG 540
CCTGCCTCAG GGATGCGATC TGAGGGAAGA GGCAGCTGTG TCTGGGAGGC CGTTCGGTCG 600
GAGGGGGATA GGCACAGCCC CTGCCCTTGG GGAAGCGCCC AGCAGCAGCC TTCAGGGAAG 660
GCAGTTTGGG GGTTTGCCGA GGGCCAGGAA GACCCTCTGC CGCAGTTAGT ATTCGATGGA 720
ATGGCTTGTG CAGAGGGAGC TGCAGAAGCT GCCATTTCTC TGGGTTAGGG GCTCCCACAG 780
CCTTTGGATG CCGGGTCTCG GCCATGAGCC CCCTCCGCCA CCCCTCCCCC AGGTCACCTT 840
GCTCAATCCA GGAGGCCGGA TGATCAGAGT GTGTTCTGCA AAGGAGCGTG AGAATCACTG 900
GGGAGATTTC CTTTTTCTTT TTCTTTCTCT TTTTTTAATG GTACAGCTTC CTGGGCCCAC 960
CCCTGAGATT CTGCACTTGT TTGGGGAGTG GGTGTTGGCT TCATGACAGG CACCCCTGGG 1020
TGCTTTGGAC ACAGGCAGTG AGCTCCCCCC ACACTGTGTG AACCCCTGAG AAGGCTTCTC 1080
CTTTTGTCTA GGGTGCCTGG GAGTCTGCTC CAGCAGCAAA CCGGGGAGGG GAGGGGTACT 1140
GGGACCGAGT GTGTGTGGCA GCACCGTGTC CAGGCAAACT GAGGCTCCAG ACGGGGGTTA 1200
CTTCTTCAGA CCCTGTTATG CAGCATGGTT CCCACTGCCC GTGCCCAGAA TTCACCATAG 1260
CTGATGGGCC TGGGGTGGGC CTCCGGGGCA GGCCAGGGTG GAAAGTGCAT CTGTGTTTGA 1320
GCTTTGCGGC CCTGGCGCTG GAGTTAGATC CCTACAGGAA AGGACATTGT AACCCAGCCC 1380
GTGGTTGAGA CTAGCAGCTG CTGAGCACCT ACGCCCTGCT AGGCTGTGGG GCAACAGCAA 1440
AGGGTAACCC CCAGCCTGCA GCCTCAGGGG GGCTTCCCAT CTAGCGAGGG GCCCAGGGAG 1500
GCCATGAGGA GAGCCATGAG GGAGGAAGGT GGGGACTCTG GGCCTGAGTG ACTCCTTCAG 1560
GGTGGGGTGC GGGCAGGGAG CCTTCAGGAG GGAGGGTACT GCCTGAGCAG GGCTCTTAAG 1620
GGACACGTGG AATTTGTTAC AGGAAGCACC AGGCCATTCC AGGCATAGAA ATCAGCTGGG 1680
GTGCAAAGGC CTGGGGGTCA GAAGAGTGGC AGATTGCTCC ATGGCAGGAA GCCCCAGCTC 1740
CTCTGGGTCG TTCCCGCTGA GGGATTCCAG CTGTTGGCAC CGAGGGGTGC AGCCAGGGCA 1800
GGGTGGTGCT GCCTGCCAGG CTGAGGTGGG AGACAGCTGG GTTTCTAGCC CTGCTTGTCA 1860
CTCGCTATAG GTGCAGCCAA ACGCTCAGCA GGCCCAAACT CTGGGCAGTC CTGACTCCCA 1920
GGCAGTGCTG TGAGGAAGGG GAGGAGGAGG CACACTGAAC CCACCTGCTA CGTTGGCTGG 1980
TGGAAATTTG GCCAGGTCTG CACTGGCCCA GCGGTGCTGG 2020