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

TagContent
EnhancerAtlas ID
HS142-00848 
Organism
Homo sapiens 
Tissue/cell
NCCIT 
Coordinate
chr1:144991400-144994590 
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
CACACACACA CACACACACA CAGACACACA CATATATATA TAAATAATTA GCCAGGTGTG 60
GTGGCACACC TGTGGTCCCA GCTACTTGGG AGGCTGGGGT GGGAGGATCA TTTGAGCCCA 120
GGAGGTCAAG GCTGCAGTGA GTCGTGACGG TGCCACTGCA CTCTAGCCTG GGTGACAGAG 180
CGAGACCCTG TCTCAAAAAA TAAAATAAAC CAGAACGGCT CTAGTTCCTA TCAATCACTC 240
ATCATGACAT AGTGTGGTAA ACTAATTTCA ACTCTGAATG ATTGATAATG GCTTTATGTG 300
TTCTGTTTCC CAAGTAATAA GAACATTTTA GCACAAGCCT TTAGCGCTTT TCAAATAATC 360
ATAGCCAAAT GAGAAAATTA ATATGACAGG CAGATTGAAC AAACATTTGG TGAGAAGGAA 420
GAGGAGGGGA TACAGTAGTT TGAGATCCCT CAAATCATAT GATGCAGTAG CTGCCTGACA 480
ACTCTGCTAA CACGTAAGAC TAGATAGAGA CAGGGCCATA TCTACTTCCT GTATGGGACC 540
CATGGCAATA CTAGAGTCTA GCAAAAGGGT TGTCCTCTCT GCATGTGACA ATAGGCTGTG 600
TTCCACTCCC CCCACATACA CCTTGTGCAG CTCCTATAAT CTCATTTATC ACACTTCTCC 660
AGGTGAGAAA TGGTGCCTTC TCACACCCCA CCCAAAGTTG TTTCCTAAAG ATCTTTCGCT 720
AGGGCGGAGC AGAGAGTGAG ATCAAATGAT TCAGACAGCC ATCTGATTCA GCTTTAAAAA 780
AAAAAAATCC TGGTGGGGGC GCAGTGGCTC ACGCCTGTAA TCCCAGTACT TTGGGAGGCT 840
GAGGCGGGTG GATCGCCTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTAAAAC 900
CCCGCCTCTA TTAAAAATAC AAAAATTAGC CAGGTGTGGT AGCAGGCGTC TGTAGTCCCA 960
GCTACTCCGG AGAATCGCTT GAACCCAGGA GGCGGAGGTT GCAGTGAGCT GAGATCGTGC 1020
CACTGCACTC TAGCCTGGGC GACAGAGTGA GACTCTGTCT CAGAACAACA ACAACAACAA 1080
CAAAATCCTT TCCCTCAAAT TACCTAAGAA ATTGTCCTTT CCTTCTTTGC CCTGAAGACA 1140
GTTAATGGGG AAAGTTCCTC CCTCTGCACA GTGAATAAAT CCATCCACTA TTCCTACCCT 1200
AACCCTAAGG CAAAACCTCC CACTCATCCT CTGTCTCTCG CCATCTCTCT GTTACCAACC 1260
CTCACTTGGC AATATCCTTC TTGACACGTG GCAGCTCCAA TGAGGCACAC TCATTACATA 1320
GCCACGTAAA AGATAAAAGG TGAATCTGGA CCAACTTCTG GAAAATTTGG ACTTAAAACA 1380
TGGAAATGCA GGAGAGACAG GAAATAGAGT TAAATCCCCC AGATTTAGCT ATACACATTA 1440
ATTGAATTAA CTAAATAATC ATTTGGGTCT CATAGACACC AGCTATTTCC CTGATCCAAG 1500
ATGTTATCTA GCAGCCTGTA TCGCTTCCCA GTCATCCATC CTCTTGACAG GACAGAGCAC 1560
ACATAGAAAA TGGTATTTGT ATAGTCCTCT GGGGTAAACA GTTGGAGAGT TAGAATCTCT 1620
GATAAGGTCA GAGGCAACCA GTCCCCGGTC ACTTGGGCCA CTTCAGGTCC TGCTTGTCCA 1680
GACACAGAGA GGGCTGAGGA AACCAATATT GTGGTGACCA GCTACGAGGC TTAATCCTCA 1740
TAACCCATAG CCCAATGTCC TCTTATCAAG GTGCTGTCCT ATCTCACCCA CAGCTCAGCC 1800
AATCCAGTAG GTCTTCCTTC CCCACCCTGA TCACTGACCC ATCAATCAAG ATAGCCCTCC 1860
CATCCAAGGA AGAGGCCATT TCCCCTCCCA CTCCACCCAG GCCAACTGCT ATCCCACAGG 1920
TTACTCTCTT CTTCATTTTA AGGCAAGCTA TTCCAAAGAC TAAAAATGCC TAAGATTCTG 1980
TCTTAAAAGC TTATCTGCAT AGTCATCTTC AAAAGCAAAC ATGAATTTCT CAAGGAACGG 2040
AAACACCCTT AGCCCCTGCC CTTTTCTCCA TAGCATCATT CTCTGCCCCA CCAAGCCGGA 2100
ACTAGGAGGG CACTTTCTCT AGGAGAGGTA TGACCTGGAG ATGATCTGCT TCAGAGCCAC 2160
CTCAGGGATC TTGCTTAAAA ATGCATATTT TCCCAGGCAA AGTGGCTCAT GCCTATAATA 2220
CCAACAACAG TGGAGGCTGA GGTGGGAGGA TCTAAAGGCC AGGAGTTTGA GACCAGCCTG 2280
GACAACATAG TGCCACCCCT TTGGTACGAA TTTTTTTTTT TTTTTTTTTT GAGACAGACT 2340
CTTGCTCTGT CACCTAGGCT GGAGTGTAGC GGCGCAATCC CGTCTCACCG CAACCTCCGC 2400
CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCAAG TAGCTTGGAC TACAGGCATA 2460
TGCCACCACA CCCGCTAATT TTTGTACTTT TTAAGTAGAG ATGGAGTTTC ACCATGTTGG 2520
CCAGGCTGGT CTCGAACTCC TGACCTCAAG CCTTCTGTCT TCCTTGGCTT CCCAAAGTGC 2580
TGGGATTACA GGCATGAGCC ACTGTGCCCT GCCAATTTTT TTTTTTTTAA TTATCTGGGC 2640
CTGGTGTCCT GTGCCTGTGG TCCCAGCTGC TCAGGAGGCT GAGCCAGAAG GCATCACTTG 2700
AGCCCAAGAG TTGGTGGCTG CAGTGCTATG ATGGTGACAC TGCACTCCAG CCTGAGCAAC 2760
AGGGCAAGAA CTGTTTCTAA AATAAATAAA TTTTAAAAAT GCAAATATCC ACCCCAGCCC 2820
CACCCTCTCC CCCCACCTTC CCCCACATTA CTACATCGGA ATCCCTAGGG TGAGGCATGG 2880
AATCTACATT TTAAACCAGC TCCCAAGGTG ATTGTTCCGC ACAGTTCCAC GTCAGTGTTT 2940
GAGAGAGGCT CTGATTTATT CCAGTCCTCT TTCTTTACAG AGAAGGAAAG CAGAAAGCAG 3000
GCACCAGAGA GGTGAAATGA GCTTGTCCAA GGTCACAGGT TGTTAAGGTG ACCAGAGCTG 3060
GACGAAACCC CACCTCTCTC GCTGACTAGC ACAGCGCCAG CTAGGAAGAG CCTAGAATAG 3120
CGACCAACTG GCAGGCCAAA CCGTCCCCTG CCCCTGCCCC TGCCTCGGAG AAGCGGGCCC 3180
CTGCACTCAC 3190