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

TagContent
EnhancerAtlas ID
HS052-01133 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr1:43414720-43417220 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:43415014-43415029TGAGGTCAGAGGGCA+6.95
Nr2f6(var.2)MA0728.1chr1:43416427-43416442GAGGTCAGGAGTTCA+6.22
RARA(var.2)MA0730.1chr1:43415171-43415188TGACCTTAGGGTGACCT-8.36
TBXTMA0009.2chr1:43416983-43416999TAACATGTATGTGTTA+6.01
TBXTMA0009.2chr1:43416983-43416999TAACATGTATGTGTTA-6.04
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_02447chr1:43414805-43416460Astrocytes
SE_05390chr1:43414707-43416429Brain_Cingulate_Gyrus
SE_05390chr1:43416630-43422108Brain_Cingulate_Gyrus
SE_08269chr1:43416936-43421988Brain_Inferior_Temporal_Lobe
SE_10377chr1:43414592-43420061CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_13825chr1:43414724-43417463CD34_Primary_RO01536
SE_14471chr1:43414700-43422138CD4_Memory_Primary_7pool
SE_20345chr1:43414766-43416518CD56
SE_20345chr1:43416921-43422093CD56
SE_20799chr1:43414730-43416336CD8_Memory_7pool
SE_22754chr1:43415217-43416365CD8_primiary
SE_22754chr1:43416585-43422072CD8_primiary
SE_23189chr1:43414912-43415861Colon_Crypt_1
SE_23904chr1:43415177-43415524Colon_Crypt_2
SE_26580chr1:43414679-43416464Esophagus
SE_33837chr1:43414630-43417352HCC1954
SE_36013chr1:43414709-43416491HMEC
SE_37191chr1:43414563-43417036HSMMtube
SE_39883chr1:43414765-43416522K562
SE_39883chr1:43416567-43420030K562
SE_41038chr1:43414730-43416507Left_Ventricle
SE_41620chr1:43414783-43415774LNCaP
SE_50202chr1:43414810-43415792Sigmoid_Colon
SE_57417chr1:43415150-43415765VACO_503
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43414873-43416676HSMM
SE_64340chr1:43414814-43416461NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14341571943416249
Enhancer Sequence
AGAGCAAGAC TCTGTCTCAA AAAAAAAAAA AAAAAGTACA AAAATTAGTG GGGTGTGGTG 60
GCACATGCCT ATAATCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATAGA ATCACTTTAA 120
CCTGGGAGGC GGAGGTTGTA GTGAGCAGAT ATTGCACGAC TGCATTCCAG TCTGGGCGAC 180
AGAGTGAGAC ACTCTCAAAA GAAAAAAAAA TAAGACAGCT TTGGCTGCAA TAAGAAAGAA 240
AGAAGCTCAA GAAATTGCAG ACTGCTGTAA CATCGGCACT TGACAGGAGG CACCTGAGGT 300
CAGAGGGCAG GTGCCCAGCC TAGCATACAA ACAAAAGCCA GGGTTGGGAC TAGAGTTGTT 360
TGGTTTCCTA GCCTGGCATT CTACCCTCTG ACCGGTTCCA TCCTGCCAAG CCTTTTAAAA 420
AAGAAGAGTG ATGGACTAAC AGTCCAAAAC CTGACCTTAG GGTGACCTCA AGCATTAAGT 480
GCTCCTGAAG CCACTTCCTT TAAGCCTTCC AATGATATCA AGACCCTTGC ATGACTGAAC 540
CTCCAGACAC CCCTGGTTGC CCTCGAGGCA GAAGGCACTC GCCAGTCTTC AAAGTAGAAC 600
TGAGAGGAGG GGGCTGGTGC ATTTAGCAGC AGCAGCAGCA GCGAGCTGAG GCACCCTGCC 660
AGAGGCTGCT CACACATTCT GATTAACCAC CATGAACAAG CTTTTGGGGA GCGATTACTC 720
CCTTTTCACA GATGAGAAAT GAGAGAGAGG GAAAAGCGCA GAACCAGGGG ACTCTAGGCT 780
TCAGGGAAGT TTCCAATTGG GGGTCTCTGA TGCCAAATTC TATGGCTTTC CTGCTTAGGT 840
CCTCCCCCTT GTTTCCGGGT ACTGGTCCCT GAAGGAAACA AGGTTTCTAC CTGGTGCTTT 900
CTATGTAGGT CAAATTCCAT AAAAGCAACT CTCTGAGCCT TGCCCACTCT GAGCTGAGAC 960
AGCCCGGGCA CAGGCTCAGA AACCTTTGGG CCACTTTGCT GCATTTGCTA TAAGCCAAAG 1020
TTGGCAAACT ATGGCAGCTA AGAATGAGTT TTACATTTTT AAGTAGCTGG GGAGAAAAAA 1080
AAGACAATGA CTAATATTTT GTGATATGTA AGAATTATAT TAAATTCACA TTTCAGTGAC 1140
CATGAATAAA GTTTTATTGG AACACAGCCA CACTCATTTG TCTACAGCTG CTTTTGTACT 1200
GCAACAGCAA AGCTGAGTGG CAGGCCGAGA ACTACATGTC CAACAAAGCT GACAATATTT 1260
ACGCTCTATC TGGCCCTTTA GAAAAAAGTT GATCGGCCTC TGCTTTAAGC CCCACGTCCC 1320
CTGAGCTAGC TGCCCAGCAT TCTCAAAGCC TTCCAGGCAA AACCACATCC TCCCTAAATA 1380
ACCGAAAAGG TATGCATCCT ATTATGGAAT GTTAAATGTA AATGGCTCCT TGGCCATGTG 1440
TGGGTGTGGG GCCAGGATCT GGACCCTGGG GAAACTGACA CCCCTGAGAA GATACACATT 1500
TGGTGGTGAG ATGGGCAATA ATTCAACTAA GAGAACATTA ATTTGGTAAG ATTGGGCACA 1560
TGCAAAGTTC ACTGTCACTC TCAGCAGACA CATTTAAGTC CCAGCTCCTC CACTTGTGTG 1620
ACCTTAAAAA AGTCCTTTCC TGGCTGGGCA TGGTGGCTCA CGCCTGTAAT TCCAGCACTT 1680
TGGGAGGCTG AGGTGGGCGG ATCACCTGAG GTCAGGAGTT CAAGACCAGC CTGACCAACA 1740
TGGTGAAACC CCGTCTCTAC TAAAAATACG AAAAATTAGC TGGGCGTGGG GGGCGCGCGC 1800
CTGTAATCCC AACTACTCGG GAGGCTGAGG CAGGAGAATC ACTTGAACCC GGGAGGCAGA 1860
GGTTGCAGTG AGCCGAGATC GCGCCATTGC ACTCCAGCTT GGGCAACAAG AGTGAAACTC 1920
CGTCTCAAAA AAAAGTCTCT TCCTCTAAGC TTCAGTTAAT TCTCCATAAG AGAGGATCTT 1980
CTATGAATAA ATGATATTGC TAAGGAAAGA TTATGCCTGA ATGCATGCTC CCAACACTCT 2040
TCTAGTCAAT GGAAATTCAG CGATAAAACT ATACCAAATC CCTGCCTATG GAACTTGATA 2100
GGTTAGTTGA AGGCTGGGGC AGAAAATAAA TACATGTAAT ACATCAGGTG GTGAGTGGTA 2160
TGAAGAAGGT GATGGGGCTG CTATTTCTTA ATCATGGTGG GACATGCCTG TAATGAAGTA 2220
TTATGCAGCT ATTGGAAAGA ATGAAACACA TCTGTGTTTC ACATAACATG TATGTGTTAT 2280
GAAGAGTACC AGGGTAGATT GTTCAGGGGG GAAAAAAAGC AATAGGATGT ACATATTGTG 2340
TAAGGAACAG GGAGTTAGTG AACTTGTATA GTGGCACTTG GTTGTATGTG CAGAGAGAAA 2400
CACTGCCAGT ATTTACCTCT AAGGGTTGGT TTGGTGAACA GAATGGGTTG CAAAGAACTA 2460
TGCAGAAAGT GGGATCCAAC TACACAAATA TTCTATTTAT 2500