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

TagContent
EnhancerAtlas ID
HS117-00507 
Organism
Homo sapiens 
Tissue/cell
LHCN-M2 
Coordinate
chr1:157979160-157982090 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:157980504-157980522CCTTCCCTCCTCCCTCCC-6.84
ZNF263MA0528.1chr1:157980677-157980698AAGGGAGGAGAGAGAGAGAGA+6.1
ZNF263MA0528.1chr1:157981692-157981713CCCTCCCCCAGCTCTTCCCCC-6.1
ZNF263MA0528.1chr1:157980680-157980701GGAGGAGAGAGAGAGAGAAAA+6.81
ZNF263MA0528.1chr1:157980499-157980520TCCACCCTTCCCTCCTCCCTC-6.83
ZNF263MA0528.1chr1:157980503-157980524CCCTTCCCTCCTCCCTCCCCT-6.83
ZNF263MA0528.1chr1:157980496-157980517CCCTCCACCCTTCCCTCCTCC-8.51
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00315chr1:157974956-157984543Adipose_Nuclei
SE_01211chr1:157976230-157981897Adrenal_Gland
SE_01670chr1:157974654-157985670Aorta
SE_02446chr1:157978714-157982051Astrocytes
SE_03108chr1:157977092-157980749Bladder
SE_03108chr1:157980802-157981880Bladder
SE_26124chr1:157976187-157982785Duodenum_Smooth_Muscle
SE_27494chr1:157976137-157982445Esophagus
SE_29957chr1:157977119-157982405Fetal_Muscle
SE_36687chr1:157977987-157982027HMEC
SE_37682chr1:157977849-157982391HSMMtube
SE_38639chr1:157977529-157982301HUVEC
SE_38884chr1:157976105-157985668IMR90
SE_42820chr1:157976155-157982360Lung
SE_45055chr1:157976934-157982562NHLF
SE_45978chr1:157970192-157985524Osteoblasts
SE_46705chr1:157979154-157980456Ovary
SE_46705chr1:157980755-157982317Ovary
SE_47236chr1:157974787-157993863Panc1
SE_49377chr1:157977166-157982064Right_Atrium
SE_50762chr1:157976039-157985489Sigmoid_Colon
SE_52052chr1:157978753-157982032Skeletal_Muscle_Myoblast
SE_55987chr1:157977524-157982749u87
SE_63841chr1:157978600-157982192HSMM
SE_68036chr1:157938003-157993230TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1157980631157980890
Enhancer Sequence
TCATTGGTAA ATGGGAATCT TGAAAAGACT GGTGACAGTA TATGCAAAAC AGAGCCTCTG 60
ACCCATGATA GGTGCTTAAC AAATGGTGGC TGTTGTTACT ACTACCATTA TTATTACCAC 120
CATACATGAA AGCACCTGGC TTAGCAGACA GCACATAAAG CAAGTTAGTT TCTTAACAAG 180
TTTGTGAGGG AGGGAGGGTC CTTTTGTTCT ACTTCCTCGA AAAAGGAGGG AAGGCACACA 240
ATTTCTACCT TGTGCTGCTT CTAGGGTGTG CTATTGAGAA AAGTCATGGC AGCCTGTTCT 300
GGTATAATTC TTCTTTCCAC AAATAAATTG CCTGTTCAAG CTGGGGCTGC TTCTGGCTGA 360
AAGCTCATTG GCACCCAGCT CCAAGCAAGG CTGATCTTGC CTCTGCCGCC TGCCAGACCT 420
CAGATTGCCC ACCTCAAGCC TGTGTGCCAA AGGGTTAAAC ATAGCGAGTT AAACATAAAA 480
GGGTTAAACA TATCACATGG CTTGCAACTT CTGACTCAGC TTCTGGTTTC CTGGGCATTA 540
CAATAGGAAC ATCTATATTC AGGAGGCAGT ATGGAAAGAG CACTGGATTG CAGGTCTAGA 600
TGTGGATTTT AGCCCCATTT GTGCCTCTAC TGGAGAGACC TTACTCAGTG ACCTGGGCCT 660
ATTTTCTTAT CATAAAATGA GAAGGTTAAT TTCCAAGATT CTTTCTGGCT GCACAGTTTT 720
CCAACTCCTT CCTATCCGGT AAGAGTTCAT GAAAAGGACT GGCTCTTCCC AAATGAGGCC 780
CTGGATCTCT CTGATTTGGT TTATAAGCCA AGGCCAGAGG TACTGATTTC AGAGGGCCAG 840
AGCAGGGGTA TCCCAGGAGC AGCGTTTGCT CAGGAACCAG GGTGGAAGCA AACATTTCAT 900
GCATCTTCAG ATCTGGTCTG AACTTGGGGT AAGGAGAGCA GGAGTCCCCA CCATAAACAC 960
ACACACACAC ACACACACAC ACACACACAC ACCCCACACA GTCCTGAGAA TGTCACACAC 1020
ATGCATACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC 1080
ACACACACAC TGTCCTGAGA ATGTCCCAGC CTGCCCTGGA AGGTGGGGAC CTGGACCAAC 1140
GGTGTGGGTG CTTGTGTATG CATGTTGATA AGAGTTTCTC CCCGAAGAAA CATGCTCTGG 1200
CTTTGCCCTG AACTTTAGCT TTGGTCTATG AAAAGGTTTT GCTGAATCTT GTGGGAACAT 1260
AAACATTCGG CAGATTTCTT TCCCTGAAAG CTATTTCTTC TCTTTTTCTG GGAACTTTTG 1320
CCAGCAAGAT CAAGGGCCCT CCACCCTTCC CTCCTCCCTC CCCTTTGCCT GAGACACCCA 1380
ACCCCCTTTC TCCTCCTCTC CTAAATGAAA ACAAAGTTAA CTGGTGTGTA CTGGGAATCA 1440
TTTCAGAGCA AACTGGGCCA GAAGAAAGGA GTAAAGCAAA CAGATAGCTC TCCCAAGAGG 1500
AGAAATTATA AGAAGGGAAG GGAGGAGAGA GAGAGAGAAA ATAAGCCAAT GGCATCAGTG 1560
GTGAAAAGTG AATTCCAGAC ATTTAAAATT CTTTTGGTTT TAATCATCTC AGAGGCTGAC 1620
CAGAGCTGAG CTGTGGGGGC AGGGAAAAAA TGAAAACCAG GGCCCTCTAC TTGGAGCGGG 1680
CTGGAATCTC AGATTGTCTG CAAAGACCGA CAGCCTTCCT ATGCAAGCTG CTCACTCTTC 1740
TCAGCCCAGG CCCTCATGAC CTCCTGTGTC TGACTGCAGA TGGTTTACCG CCTCCGGAGA 1800
GCCCATCCTG ACTAACCCTC TCTTTTTATC TCACTTTACA CTCGGTTTTC AAGCACTGAC 1860
CTTTCAGTTT TCCAACCGGA TTGCAAGTTC CCCAAGGCCC TGGATTATGT TTTGTTAAAA 1920
GCAAAACTAA CAAACGACAA ACCAAAGCCT CTTTCATAAT TATGCCTTGG TCCCCTGCGT 1980
GAGGGTTGGA CCCTCGGAGA AGCCCCAAGG CCTCTTCCTC ATCTGTAAAA TGGGCTGAAG 2040
AGCTGAGCCC AGCCTTGAAG AGACTCTAGA AGGAACCGGA AGCTGGGAGA AGCCTAGCGG 2100
CTGGTGCCTC CTCTGTGCTG TGCTCTATTG GGCACTTCAG GATTCTCTCA AGGCTGCCCT 2160
GTGGGAGGGG TTGGAGGCAT TTCGCTGAGG CCTAGGGGAA GTAGAGGGTC TTATTGTCCC 2220
CTTTCTCAGG GGTAGGTCTG GTTGGCAGTG GGTGAAGCTC CTGGACACAG GTGGCTGGGA 2280
GATGGGATGG GGGATTCCAG GCTCTCTCCT TCCCTGGGCC ACAGTGGGTT TTAAGGTGAA 2340
GGAGGGAACC AGGAAATCTT GCCAGCTGTG GAGAGGTGAT TGGTGGGAGG ACCGGAGGGC 2400
AGCAGTGGGG GAAGGAGCCT GGAGGAGAAG CAGGAGGCCA GGCAGTGGCC ACGAGGACGT 2460
AGTCACACGC AGAAGCCTCC TTTCCCTGGA CCGGGTCCCC TCTGTGGTCA GCATCTTTCT 2520
TCTTTCTGAG CTCCCTCCCC CAGCTCTTCC CCCTCAATGT TGAGCTCTCA GTTTCTTTCT 2580
CCATCTGGAG GCAGCTCTCT TCATTCTCAT GACCACCAGC TGTTTCTCCC ACTTTCCCCC 2640
TCCCACTTTC CCTCAAACTT TGATTCCTGG GCCTTTGGAC TTAGGTCTGT TTTTCATAGT 2700
GTATCTCCCA CCCCTGCTTC CCTTCCCCAA TAAGATTAAA AAATGTAGAG CTTGAGGGTA 2760
GATTAGAGTT GACCTTAGAA TAGGAGTCAG GTGACCTGGA TTTTAATCTC AACTCGTCTT 2820
ATTGGACTGC TTTCTCTTGG GCAAGACATG TGCTTTTTTG GGGCCTTGGT TTATTCAGTA 2880
GTAAAATGAG GAGCTCCGTA AATGATGCCT GAGGCCAGAT GCTTTTCACC 2930