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

TagContent
EnhancerAtlas ID
HS030-01540 
Organism
Homo sapiens 
Tissue/cell
CyT49 
Coordinate
chr1:144991350-144994590 
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
ACCTCAATCT CTGCCAAAAA AAAAAAAAAA AAAATACATA CACACACACA CACACACACA 60
CACACACACA CAGACACACA CATATATATA TAAATAATTA GCCAGGTGTG GTGGCACACC 120
TGTGGTCCCA GCTACTTGGG AGGCTGGGGT GGGAGGATCA TTTGAGCCCA GGAGGTCAAG 180
GCTGCAGTGA GTCGTGACGG TGCCACTGCA CTCTAGCCTG GGTGACAGAG CGAGACCCTG 240
TCTCAAAAAA TAAAATAAAC CAGAACGGCT CTAGTTCCTA TCAATCACTC ATCATGACAT 300
AGTGTGGTAA ACTAATTTCA ACTCTGAATG ATTGATAATG GCTTTATGTG TTCTGTTTCC 360
CAAGTAATAA GAACATTTTA GCACAAGCCT TTAGCGCTTT TCAAATAATC ATAGCCAAAT 420
GAGAAAATTA ATATGACAGG CAGATTGAAC AAACATTTGG TGAGAAGGAA GAGGAGGGGA 480
TACAGTAGTT TGAGATCCCT CAAATCATAT GATGCAGTAG CTGCCTGACA ACTCTGCTAA 540
CACGTAAGAC TAGATAGAGA CAGGGCCATA TCTACTTCCT GTATGGGACC CATGGCAATA 600
CTAGAGTCTA GCAAAAGGGT TGTCCTCTCT GCATGTGACA ATAGGCTGTG TTCCACTCCC 660
CCCACATACA CCTTGTGCAG CTCCTATAAT CTCATTTATC ACACTTCTCC AGGTGAGAAA 720
TGGTGCCTTC TCACACCCCA CCCAAAGTTG TTTCCTAAAG ATCTTTCGCT AGGGCGGAGC 780
AGAGAGTGAG ATCAAATGAT TCAGACAGCC ATCTGATTCA GCTTTAAAAA AAAAAAATCC 840
TGGTGGGGGC GCAGTGGCTC ACGCCTGTAA TCCCAGTACT TTGGGAGGCT GAGGCGGGTG 900
GATCGCCTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTAAAAC CCCGCCTCTA 960
TTAAAAATAC AAAAATTAGC CAGGTGTGGT AGCAGGCGTC TGTAGTCCCA GCTACTCCGG 1020
AGAATCGCTT GAACCCAGGA GGCGGAGGTT GCAGTGAGCT GAGATCGTGC CACTGCACTC 1080
TAGCCTGGGC GACAGAGTGA GACTCTGTCT CAGAACAACA ACAACAACAA CAAAATCCTT 1140
TCCCTCAAAT TACCTAAGAA ATTGTCCTTT CCTTCTTTGC CCTGAAGACA GTTAATGGGG 1200
AAAGTTCCTC CCTCTGCACA GTGAATAAAT CCATCCACTA TTCCTACCCT AACCCTAAGG 1260
CAAAACCTCC CACTCATCCT CTGTCTCTCG CCATCTCTCT GTTACCAACC CTCACTTGGC 1320
AATATCCTTC TTGACACGTG GCAGCTCCAA TGAGGCACAC TCATTACATA GCCACGTAAA 1380
AGATAAAAGG TGAATCTGGA CCAACTTCTG GAAAATTTGG ACTTAAAACA TGGAAATGCA 1440
GGAGAGACAG GAAATAGAGT TAAATCCCCC AGATTTAGCT ATACACATTA ATTGAATTAA 1500
CTAAATAATC ATTTGGGTCT CATAGACACC AGCTATTTCC CTGATCCAAG ATGTTATCTA 1560
GCAGCCTGTA TCGCTTCCCA GTCATCCATC CTCTTGACAG GACAGAGCAC ACATAGAAAA 1620
TGGTATTTGT ATAGTCCTCT GGGGTAAACA GTTGGAGAGT TAGAATCTCT GATAAGGTCA 1680
GAGGCAACCA GTCCCCGGTC ACTTGGGCCA CTTCAGGTCC TGCTTGTCCA GACACAGAGA 1740
GGGCTGAGGA AACCAATATT GTGGTGACCA GCTACGAGGC TTAATCCTCA TAACCCATAG 1800
CCCAATGTCC TCTTATCAAG GTGCTGTCCT ATCTCACCCA CAGCTCAGCC AATCCAGTAG 1860
GTCTTCCTTC CCCACCCTGA TCACTGACCC ATCAATCAAG ATAGCCCTCC CATCCAAGGA 1920
AGAGGCCATT TCCCCTCCCA CTCCACCCAG GCCAACTGCT ATCCCACAGG TTACTCTCTT 1980
CTTCATTTTA AGGCAAGCTA TTCCAAAGAC TAAAAATGCC TAAGATTCTG TCTTAAAAGC 2040
TTATCTGCAT AGTCATCTTC AAAAGCAAAC ATGAATTTCT CAAGGAACGG AAACACCCTT 2100
AGCCCCTGCC CTTTTCTCCA TAGCATCATT CTCTGCCCCA CCAAGCCGGA ACTAGGAGGG 2160
CACTTTCTCT AGGAGAGGTA TGACCTGGAG ATGATCTGCT TCAGAGCCAC CTCAGGGATC 2220
TTGCTTAAAA ATGCATATTT TCCCAGGCAA AGTGGCTCAT GCCTATAATA CCAACAACAG 2280
TGGAGGCTGA GGTGGGAGGA TCTAAAGGCC AGGAGTTTGA GACCAGCCTG GACAACATAG 2340
TGCCACCCCT TTGGTACGAA TTTTTTTTTT TTTTTTTTTT GAGACAGACT CTTGCTCTGT 2400
CACCTAGGCT GGAGTGTAGC GGCGCAATCC CGTCTCACCG CAACCTCCGC CTCCTGGGTT 2460
CAAGCAATTC TCCTGCCTCA GCCTCCCAAG TAGCTTGGAC TACAGGCATA TGCCACCACA 2520
CCCGCTAATT TTTGTACTTT TTAAGTAGAG ATGGAGTTTC ACCATGTTGG CCAGGCTGGT 2580
CTCGAACTCC TGACCTCAAG CCTTCTGTCT TCCTTGGCTT CCCAAAGTGC TGGGATTACA 2640
GGCATGAGCC ACTGTGCCCT GCCAATTTTT TTTTTTTTAA TTATCTGGGC CTGGTGTCCT 2700
GTGCCTGTGG TCCCAGCTGC TCAGGAGGCT GAGCCAGAAG GCATCACTTG AGCCCAAGAG 2760
TTGGTGGCTG CAGTGCTATG ATGGTGACAC TGCACTCCAG CCTGAGCAAC AGGGCAAGAA 2820
CTGTTTCTAA AATAAATAAA TTTTAAAAAT GCAAATATCC ACCCCAGCCC CACCCTCTCC 2880
CCCCACCTTC CCCCACATTA CTACATCGGA ATCCCTAGGG TGAGGCATGG AATCTACATT 2940
TTAAACCAGC TCCCAAGGTG ATTGTTCCGC ACAGTTCCAC GTCAGTGTTT GAGAGAGGCT 3000
CTGATTTATT CCAGTCCTCT TTCTTTACAG AGAAGGAAAG CAGAAAGCAG GCACCAGAGA 3060
GGTGAAATGA GCTTGTCCAA GGTCACAGGT TGTTAAGGTG ACCAGAGCTG GACGAAACCC 3120
CACCTCTCTC GCTGACTAGC ACAGCGCCAG CTAGGAAGAG CCTAGAATAG CGACCAACTG 3180
GCAGGCCAAA CCGTCCCCTG CCCCTGCCCC TGCCTCGGAG AAGCGGGCCC CTGCACTCAC 3240