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

TagContent
EnhancerAtlas ID
HS081-01111 
Organism
Homo sapiens 
Tissue/cell
HACAT 
Coordinate
chr1:144991380-144994590 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2863344chr1144992176hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PHOX2AMA0713.1chr1:144992838-144992849TAATTGAATTA-6.14
Phox2bMA0681.1chr1:144992838-144992849TAATTGAATTA-6.14
ZNF263MA0528.1chr1:144994222-144994243CCCTCTCCCCCCACCTTCCCC-6.01
ZNF263MA0528.1chr1:144994219-144994240CCACCCTCTCCCCCCACCTTC-6.12
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00153chr1:144986936-144996877Adipose_Nuclei
SE_01663chr1:144992355-144995805Aorta
SE_03153chr1:144994107-144996607Brain_Angular_Gyrus
SE_03895chr1:144981928-144998593Brain_Anterior_Caudate
SE_06980chr1:144981790-144993272Brain_Hippocampus_Middle_150
SE_07793chr1:144981781-144998619Brain_Inferior_Temporal_Lobe
SE_13466chr1:144991325-144999884CD34_Primary_RO01536
SE_14437chr1:144986037-145001897CD4_Memory_Primary_7pool
SE_20767chr1:144988301-145005247CD8_Memory_7pool
SE_25864chr1:144981619-144993933Duodenum_Smooth_Muscle
SE_29575chr1:144986139-144998584Fetal_Muscle
SE_36911chr1:144980899-144998579HSMMtube
SE_39856chr1:144990852-145001251K562
SE_40587chr1:144981284-144996612Left_Ventricle
SE_42105chr1:144981294-144996692Lung
SE_45547chr1:144985775-144996591Osteoblasts
SE_48047chr1:144981293-144998342Psoas_Muscle
SE_48578chr1:144991037-144996581Right_Atrium
SE_49452chr1:144991047-144992262Right_Ventricle
SE_49452chr1:144992277-144996588Right_Ventricle
SE_51073chr1:144980732-145007384Skeletal_Muscle
SE_51728chr1:144987720-144992104Skeletal_Muscle_Myoblast
SE_54547chr1:144981378-144996208Stomach_Smooth_Muscle
SE_63512chr1:144987562-144992168HSMM
SE_68443chr1:144988869-145040149TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1144992921144993173
Number: 3             
IDChromosomeStartEnd
GH01I120276chr1144993885144995952
GH01I120619chr1144993938144995956
GH01I149240chr1144994415144995898
Enhancer Sequence
AAAATACATA CACACACACA CACACACACA CACACACACA CAGACACACA CATATATATA 60
TAAATAATTA GCCAGGTGTG GTGGCACACC TGTGGTCCCA GCTACTTGGG AGGCTGGGGT 120
GGGAGGATCA TTTGAGCCCA GGAGGTCAAG GCTGCAGTGA GTCGTGACGG TGCCACTGCA 180
CTCTAGCCTG GGTGACAGAG CGAGACCCTG TCTCAAAAAA TAAAATAAAC CAGAACGGCT 240
CTAGTTCCTA TCAATCACTC ATCATGACAT AGTGTGGTAA ACTAATTTCA ACTCTGAATG 300
ATTGATAATG GCTTTATGTG TTCTGTTTCC CAAGTAATAA GAACATTTTA GCACAAGCCT 360
TTAGCGCTTT TCAAATAATC ATAGCCAAAT GAGAAAATTA ATATGACAGG CAGATTGAAC 420
AAACATTTGG TGAGAAGGAA GAGGAGGGGA TACAGTAGTT TGAGATCCCT CAAATCATAT 480
GATGCAGTAG CTGCCTGACA ACTCTGCTAA CACGTAAGAC TAGATAGAGA CAGGGCCATA 540
TCTACTTCCT GTATGGGACC CATGGCAATA CTAGAGTCTA GCAAAAGGGT TGTCCTCTCT 600
GCATGTGACA ATAGGCTGTG TTCCACTCCC CCCACATACA CCTTGTGCAG CTCCTATAAT 660
CTCATTTATC ACACTTCTCC AGGTGAGAAA TGGTGCCTTC TCACACCCCA CCCAAAGTTG 720
TTTCCTAAAG ATCTTTCGCT AGGGCGGAGC AGAGAGTGAG ATCAAATGAT TCAGACAGCC 780
ATCTGATTCA GCTTTAAAAA AAAAAAATCC TGGTGGGGGC GCAGTGGCTC ACGCCTGTAA 840
TCCCAGTACT TTGGGAGGCT GAGGCGGGTG GATCGCCTGA GGTCAGGAGT TTGAGACCAG 900
CCTGGCCAAC ATGGTAAAAC CCCGCCTCTA TTAAAAATAC AAAAATTAGC CAGGTGTGGT 960
AGCAGGCGTC TGTAGTCCCA GCTACTCCGG AGAATCGCTT GAACCCAGGA GGCGGAGGTT 1020
GCAGTGAGCT GAGATCGTGC CACTGCACTC TAGCCTGGGC GACAGAGTGA GACTCTGTCT 1080
CAGAACAACA ACAACAACAA CAAAATCCTT TCCCTCAAAT TACCTAAGAA ATTGTCCTTT 1140
CCTTCTTTGC CCTGAAGACA GTTAATGGGG AAAGTTCCTC CCTCTGCACA GTGAATAAAT 1200
CCATCCACTA TTCCTACCCT AACCCTAAGG CAAAACCTCC CACTCATCCT CTGTCTCTCG 1260
CCATCTCTCT GTTACCAACC CTCACTTGGC AATATCCTTC TTGACACGTG GCAGCTCCAA 1320
TGAGGCACAC TCATTACATA GCCACGTAAA AGATAAAAGG TGAATCTGGA CCAACTTCTG 1380
GAAAATTTGG ACTTAAAACA TGGAAATGCA GGAGAGACAG GAAATAGAGT TAAATCCCCC 1440
AGATTTAGCT ATACACATTA ATTGAATTAA CTAAATAATC ATTTGGGTCT CATAGACACC 1500
AGCTATTTCC CTGATCCAAG ATGTTATCTA GCAGCCTGTA TCGCTTCCCA GTCATCCATC 1560
CTCTTGACAG GACAGAGCAC ACATAGAAAA TGGTATTTGT ATAGTCCTCT GGGGTAAACA 1620
GTTGGAGAGT TAGAATCTCT GATAAGGTCA GAGGCAACCA GTCCCCGGTC ACTTGGGCCA 1680
CTTCAGGTCC TGCTTGTCCA GACACAGAGA GGGCTGAGGA AACCAATATT GTGGTGACCA 1740
GCTACGAGGC TTAATCCTCA TAACCCATAG CCCAATGTCC TCTTATCAAG GTGCTGTCCT 1800
ATCTCACCCA CAGCTCAGCC AATCCAGTAG GTCTTCCTTC CCCACCCTGA TCACTGACCC 1860
ATCAATCAAG ATAGCCCTCC CATCCAAGGA AGAGGCCATT TCCCCTCCCA CTCCACCCAG 1920
GCCAACTGCT ATCCCACAGG TTACTCTCTT CTTCATTTTA AGGCAAGCTA TTCCAAAGAC 1980
TAAAAATGCC TAAGATTCTG TCTTAAAAGC TTATCTGCAT AGTCATCTTC AAAAGCAAAC 2040
ATGAATTTCT CAAGGAACGG AAACACCCTT AGCCCCTGCC CTTTTCTCCA TAGCATCATT 2100
CTCTGCCCCA CCAAGCCGGA ACTAGGAGGG CACTTTCTCT AGGAGAGGTA TGACCTGGAG 2160
ATGATCTGCT TCAGAGCCAC CTCAGGGATC TTGCTTAAAA ATGCATATTT TCCCAGGCAA 2220
AGTGGCTCAT GCCTATAATA CCAACAACAG TGGAGGCTGA GGTGGGAGGA TCTAAAGGCC 2280
AGGAGTTTGA GACCAGCCTG GACAACATAG TGCCACCCCT TTGGTACGAA TTTTTTTTTT 2340
TTTTTTTTTT GAGACAGACT CTTGCTCTGT CACCTAGGCT GGAGTGTAGC GGCGCAATCC 2400
CGTCTCACCG CAACCTCCGC CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCAAG 2460
TAGCTTGGAC TACAGGCATA TGCCACCACA CCCGCTAATT TTTGTACTTT TTAAGTAGAG 2520
ATGGAGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAAG CCTTCTGTCT 2580
TCCTTGGCTT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACTGTGCCCT GCCAATTTTT 2640
TTTTTTTTAA TTATCTGGGC CTGGTGTCCT GTGCCTGTGG TCCCAGCTGC TCAGGAGGCT 2700
GAGCCAGAAG GCATCACTTG AGCCCAAGAG TTGGTGGCTG CAGTGCTATG ATGGTGACAC 2760
TGCACTCCAG CCTGAGCAAC AGGGCAAGAA CTGTTTCTAA AATAAATAAA TTTTAAAAAT 2820
GCAAATATCC ACCCCAGCCC CACCCTCTCC CCCCACCTTC CCCCACATTA CTACATCGGA 2880
ATCCCTAGGG TGAGGCATGG AATCTACATT TTAAACCAGC TCCCAAGGTG ATTGTTCCGC 2940
ACAGTTCCAC GTCAGTGTTT GAGAGAGGCT CTGATTTATT CCAGTCCTCT TTCTTTACAG 3000
AGAAGGAAAG CAGAAAGCAG GCACCAGAGA GGTGAAATGA GCTTGTCCAA GGTCACAGGT 3060
TGTTAAGGTG ACCAGAGCTG GACGAAACCC CACCTCTCTC GCTGACTAGC ACAGCGCCAG 3120
CTAGGAAGAG CCTAGAATAG CGACCAACTG GCAGGCCAAA CCGTCCCCTG CCCCTGCCCC 3180
TGCCTCGGAG AAGCGGGCCC CTGCACTCAC 3210