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

TagContent
EnhancerAtlas ID
HS003-00415 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr1:16507280-16511880 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs7538216chr116509671hg19
rs36086195chr116510894hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArntlMA0603.1chr1:16510043-16510053GGTCACGTGC+6.02
ELF3MA0640.1chr1:16508229-16508242CTACTTCCGGCTA-6.25
EWSR1-FLI1MA0149.1chr1:16508479-16508497GGGAGGAAGGAAGCAGAG+6.42
Nr2f6(var.2)MA0728.1chr1:16509417-16509432GAGGTCAGGAGTTCA+6.22
STAT1MA0137.3chr1:16511012-16511023TTTCCTGGAAA-6.62
Stat4MA0518.1chr1:16511009-16511023CCTTTTCCTGGAAA-6.91
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_23091chr1:16507977-16509332Colon_Crypt_1
SE_24743chr1:16508183-16508861Colon_Crypt_3
SE_26540chr1:16504790-16512175Esophagus
SE_28102chr1:16507825-16509373Fetal_Intestine
SE_29455chr1:16507734-16509371Fetal_Intestine_Large
SE_31527chr1:16507486-16509710Gastric
SE_31527chr1:16509851-16511737Gastric
SE_34268chr1:16506936-16512113HCT-116
SE_34628chr1:16506549-16512234HeLa
SE_36144chr1:16507720-16509431HMEC
SE_38062chr1:16507125-16509874HUVEC
SE_40833chr1:16507342-16509479Left_Ventricle
SE_44998chr1:16507356-16509449NHLF
SE_46140chr1:16507347-16510631Osteoblasts
SE_47009chr1:16508039-16509386Ovary
SE_47150chr1:16499250-16512083Panc1
SE_47539chr1:16507961-16508560Pancreas
SE_47539chr1:16508587-16509159Pancreas
SE_48744chr1:16507441-16509527Right_Atrium
SE_50427chr1:16507395-16509522Sigmoid_Colon
SE_52536chr1:16507445-16509419Small_Intestine
SE_56795chr1:16507333-16512008VACO_400
SE_57357chr1:16508000-16508578VACO_503
SE_57357chr1:16508592-16509318VACO_503
SE_57939chr1:16507977-16509011VACO_9m
SE_64726chr1:16507942-16511421NHEK
SE_65472chr1:16507356-16509554Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr11650808616509162
chr11650995016510149
chr11650840216508642
chr11651086416511423
chr11651149916511858
Number: 1             
IDChromosomeStartEnd
GH01I016171chr11649794116511884
Enhancer Sequence
CTCACTGCAA CCTCTGCCTT CTGGGCTCAA GCCAGCCTCC TACCTCAGCC TCCTGAGTAG 60
CCAGGACTAC AGGTGTACAC CACCACACCC AGCTAATTTT TTGCGTGCTT TTTGTAGAGA 120
TGGGGTTTCA CCATGTTGCC TAGTCTGGTC TCGAACTCCT GACCTCAAGA GATCCACCCA 180
CCTTGGATCC CAAAATGCTG GGATTACAGG CATGAGCTAC TGCGCCCGGC CTCTAGATTT 240
AAATAGTACC TACCGAACTG GCCAGTGCAG CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA 300
GAGCTGGGCC TGGCTGTGTG TTATTCACGT TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC 360
CTCTGGCAGC AGAATCACCT GGGAAGCCAA AACTTCAGAT CCCTGGGATC CCAGACCCAC 420
TGAATCAGAA TCTCCGAGGC CAGGGCTTGG GCGTCTGCCC GTTCACCACA CACCCCAGCT 480
GATTCTGATG CACATGAGGT CAAGTTTGAA ACCCACCCCA CTGCCCTAGT TGTTCAAGAC 540
TCCCAGCGCT GGCTGGATGC AAAGTCTTAT GCCTGTAATC CCAGCTCTTT TGGGAGGCCA 600
AGGCGGGCAG ATCACTTGAG GTCAGGAGTT CGAGACCAGC CGGGCCTACA GAGTGAAACC 660
CCGTCTCTAC TAAAAATACA AAAATTAGCT AGGTGTGGTG GTGGGCGCCT GTAATCCCAG 720
GAGGTGGAGG TTGCAGTGAG CCGAGATCGC GCCGCTGCAC TGCATCCTGG GCAACAGAGC 780
GGGACTCCGT CTCAAAAAAA AAAAAAGACT CCCGGCCAGG AAGAGAGCTT GAATGAAGTC 840
TGACCTGCAC CAGGCCTTCT GGGCCCAGAC CAGGCCTGCT TAGGGGCATG TGCCCTGCTC 900
AGAACTTCCC CATCCCAGCT AACCCAGAAG ATAGCTGGGA TGAAGATAGC TACTTCCGGC 960
TACCAGCCCA TGATTCTTTG CCAGCCTGCA CTGTTCCCTG AAGAGCAAAA AGACTTGGAA 1020
TTTCCCTGCT CTATCCAGAG GGGCTGGGAT GAGGGGTCCT GAGTTCCCTT ATCCCATGTC 1080
CTACCAACCT CTGGAGCTCT CCAGTCAGCC AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC 1140
AATGGGAGGG AGAGGCTTGG CCCAGCACCC CACCCCACAG ATCAGCCTGG TCCGGCAAGG 1200
GGAGGAAGGA AGCAGAGGCA GCCTGGGCCA GCGGACACAG GGTTGGGGGT GACACAGGCC 1260
TCAGGAATTT GAAAACAAAC ACTTCGCCAG GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG 1320
CCCGGGCGGG CCCAGGTCCC TCCCTTTCAG GGCAGGGGTG AATCCCAGTG CTGCTGACCA 1380
TGGCCCCCGG CTGGACCCAG TGCTCGGGGA GTTTCCACTC CGCTGGTGGG ATGGGAAGGT 1440
CATGGGAGGT GTGGGGGGAT CCAGGCTCTG TCCAGATACG GGAGCATCCT GGCTGGGGTG 1500
AGGACAGGAA GGGACAAAGA GCTGGGAAAG CCACGAGACC CCAGGAGAAG GCTCAGCAGC 1560
AACAGGATGC CGCCTCAAGC ATTTATTGAG CACCCATGGT ATTCCAAAAA CTGAGAATAT 1620
AAGCACTGCC TAGCTGGGGA GATCAGGGGA AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA 1680
GGTGGCATTG AACTGAGCCC TGAAAGGTAA ACTAGGACCG GGGAGGACAG AATCTTACAA 1740
GTCTCCCCCC TTCACACTCC CAGAGCCGGC GCTCAGTGAG TGCATGAGTG AGTAAGCGGC 1800
TGACCAGCGA CTATGCAGCA TGAATGAATG ACAGACTGAA TGACATGAAG CCTGGAGTCT 1860
CAAGGCCGAG ACTGCAAAAG AAGAGTCCAT CCTCCTATCC CCTCTGCTCT GAACTCTCTT 1920
CATGATCCTG AAGGTGCTTG GTACCTGGAG ACTACGGAGC CAGCCTGCCG GGGTTCTAGT 1980
CTGAACTCAG TCACTTCCCA GCTGTGTAAC TTTGGACAAG TTACTTAACC TCTCTGTGCC 2040
TCTGGTCCCT TCTCTGTAAA GTGTAGTCAT CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT 2100
CCCAGCACTT TGGGAGGCCA AGGCAGACGA ATCACTTGAG GTCAGGAGTT CAAGACCAGC 2160
CTGCCCAACA TGGTGAAACC CTGTCTCTAC TAAAAACACA AAAATCAGCC GGGTGTCGGG 2220
GGCAGGCACC TGTAATCCCA GCTACTCGGG AGGCTAAGGC ACGAGAATTG CTTGAACCCG 2280
GGAGGCGGAG GTTGCAGTGA GCTGACATCT CGCCACTGCA CTCCAGCCTG GGCAACAGAG 2340
TGAGACTCAA AAAAAAAAAA AAAAAATACA GAGGTAATCA TAGTGCCTCC TTCACAGGGT 2400
TTTTGAGAGG ACTGAATGAG TTTTACAAGT GAAGTGCTTA GAACGACGTT GCACATGTAG 2460
TGAGAACTAC ATGAGTGTTG GCCAATGCTA TTACTGAGGT TCCAGCTTAC GCGTTCATTG 2520
AGTCACTCAC TCACTCACTG TTCATTCACT GATTCGCTCC TACATGCCAT CCGCCACTTA 2580
CACACCCCTC CCTCTTCACC GTCATCTGTT AAGCAATCCC CGTGTGCCCG GCTCTCTCCT 2640
CTCGGTCCTC CCAGCCCCCC TTTGCCAGTC TTGGATGGTG CCCGCCGTGC TGCCAATTAC 2700
CCTAACAATT TCATTAATTC CTCTCAAGCC CAAAACAAAC AAGAAGGACC TATCTGGAGC 2760
AGGGGTCACG TGCTAAGACC AGAAGCAGGT GTGGGACAAA CCCTCTAGGA CGAGTTCTTT 2820
GACCAGAGTT CATCACCGGA GCTGCTCCAG AGATGGCCAG GCCTCCCCAC CTGCAGGTGC 2880
CCGGCCAGTG CCCCCCACCC CGGGCAGCCT CACCCACTCC CCTCTTTGAG TAAAGGTAAA 2940
GGGACTTGCC CAAGGCTGGG TTCTCCCACA TCCCGACTGC ACCTGTCCAC ATTTCAGGCT 3000
TCATTCATGC CAGGAGCCCC AGACCTGCTC CATGCACCAG CTCCGCCCAA GCCTGGAGCC 3060
CCGGGCTGGC TGAGGTGAGA GCCCCAAAGC TCGAGCCCAT TTCAGCAGCT AACAATTAGA 3120
GCTGGTGTGA ACATGATGAC TGCATGCTGA TTAATGTAAG ATGGCTGAGC AGAAGATCCC 3180
GCCATTTCCT TCCCCACAGG CCCTGGGAGA ACAGGTCCCG CTGGGGAAGA CTCTGTCGTG 3240
TTCTGCAAAA GCCATTTCTT GAGCACGTCC TGCAGGCCGG GCACTGCGCT GGGCACTTGA 3300
TTCCTTTCAA CAGCATGACA TGGTGGGAGG ACAACTTGCC TCTCATTGAT GAAGAAACGG 3360
AGGCTCAGAG AGGTAAAGGA ACTTGCCCAA GGCCACACAG CCAGTCAGTG TGGTCCTGGA 3420
ATTCCAATCC AGGTCTTCTC TTGCTGATTC CTACCCCCAG GGATGAGCCA GTTTGACATT 3480
TGTGGAACTG GAGAGAGGCT GGGTTTGGGC ATAAGGTAAT GTTTAGGCCA GAGGGTGGAG 3540
AAGGAGAGGA CAGCCAGAGA GGCAGAGCCA AGCGCCAGGC AGGAACAATG GTACAGGGCA 3600
GGTAACGGGA GCCCGGCCAG CTCTGGGACT CCTGGGCAGG CCCTGCTGGG CCCTGCGAGC 3660
AACAGGCTCA CCCTGTGGAG CTGCCAGGGT GACAGCAGCC TCGATCTGCT GACTCAACGA 3720
GTGCATCGGC CTTTTCCTGG AAAACAGTAG ACGCAGTGTG GGTGTCGGAG GGAGGCACCT 3780
GTTTGGGAAA AGGGTGTGTG GGAACCCTGT CCTGCCCTGC AGCTCCCCAC AGCCAGTGTA 3840
CAGGTACTTA GCTCCAGGTG CCCCCCGAAC CTCCCACCAC CTGCCCAGAC CCCAGAAGCC 3900
ACCGGATCCA GGAGTCCGAG CCAGCTGTGG GCTGAGTCCA TGGTGCCACC AAGGCTCTGC 3960
ATGACCAGTG CTGCCAGCCA CCACCTCAGC CAAGCAGCAC AGCCTCTCAG GGCATGTCCC 4020
CACTTGCTGT CTGCAGAGCC TTGTTTTGCC CCACCCTGAA GGGGCAGGTG TAGACGAGCA 4080
TTGAGGCAGG TCTATGTGAC ACCACTTGCT GTCACTCTTC TTTGGGAGGT ATCAGGGCCA 4140
CTCTGCCACG GGGCACAGCT TAGGGCCTCC ATGGAATCTG GTCTGAAGGA TCCCGCTGCC 4200
CAGAGGGGGG TCAAGAATAC GGAATGGGTT CAGGAGCACC CCCTGTCTTC AGGATCCAGT 4260
TGGGGGAGGT CCCAGCAGGG CCAGTCACAG ACACTTGTCA CACCCTGGAG GGGATAATAG 4320
GATCTGGGGC TCAGCCTCCA CCAATTTCAT CACCACACAC CACACCCAGG CAAGGGAGAG 4380
CAGAGGCATC AGCAGGGCCT GGCTGAGGGG CTGAAGCCTG GTGGGGAAGC AGGGAGGGCC 4440
CCTGGGCCTC TCGGTCCTAT CTCTTCCCAA TCCAGGCCTC AGCGGACTCC AGGGCAGGGG 4500
TGCGGGAGCT GATTTCCAGG TGCAATATTC ACTGTCACCA TGGCCGCTTC CAGCACCCAG 4560
CCTGAATTTC CTAGTGCAAT GCTGGGAAGA ACTAGTCTTT 4600