EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-37250 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr7:75919380-75922400 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12113288chr775920815hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr7:75920643-75920653GGCACGTGCC+6.02
HES2MA0616.2chr7:75920643-75920653GGCACGTGCC-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00055chr7:75920207-75925655Adipose_Nuclei
SE_00909chr7:75919291-75920015Adrenal_Gland
SE_00909chr7:75920271-75921957Adrenal_Gland
SE_01790chr7:75920184-75922007Aorta
SE_03614chr7:75920349-75921211Brain_Angular_Gyrus
SE_03614chr7:75921256-75921830Brain_Angular_Gyrus
SE_04420chr7:75920256-75922069Brain_Anterior_Caudate
SE_05724chr7:75920288-75924934Brain_Cingulate_Gyrus
SE_06287chr7:75919946-75930213Brain_Hippocampus_Middle
SE_07560chr7:75920226-75925514Brain_Hippocampus_Middle_150
SE_08490chr7:75919985-75925009Brain_Inferior_Temporal_Lobe
SE_24584chr7:75921111-75921759Colon_Crypt_2
SE_26462chr7:75920316-75925507Duodenum_Smooth_Muscle
SE_26581chr7:75919218-75919992Esophagus
SE_26581chr7:75920201-75922116Esophagus
SE_29613chr7:75920891-75922015Fetal_Muscle
SE_31739chr7:75920277-75921989Gastric
SE_34164chr7:75919365-75920012HCC1954
SE_34164chr7:75920176-75922056HCC1954
SE_34396chr7:75918595-75922081HCT-116
SE_37360chr7:75920158-75925139HSMMtube
SE_38327chr7:75920219-75924904HUVEC
SE_40697chr7:75920287-75922016Left_Ventricle
SE_41779chr7:75920341-75921883LNCaP
SE_42246chr7:75920294-75922048Lung
SE_43488chr7:75920194-75921123MCF-7
SE_43488chr7:75921290-75921829MCF-7
SE_47553chr7:75920340-75920933Pancreas
SE_47553chr7:75921136-75921880Pancreas
SE_48077chr7:75920519-75922062Psoas_Muscle
SE_48614chr7:75920295-75921987Right_Atrium
SE_49587chr7:75921159-75921826Right_Ventricle
SE_50605chr7:75920286-75921996Sigmoid_Colon
SE_51109chr7:75920291-75927799Skeletal_Muscle
SE_52964chr7:75920283-75921988Small_Intestine
SE_54266chr7:75920273-75922051Spleen
SE_55401chr7:75920531-75920955Thymus
SE_55401chr7:75921215-75921697Thymus
SE_65376chr7:75920268-75925573Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr77592041675921932
Number: 1             
IDChromosomeStartEnd
GH07I076290chr77591940175928342
Enhancer Sequence
AGAAAGAAAG AAAAAAAGAT AACAAAAAGA AGCCCTCGTG ATCTCTGTAA CCCTTTCTAA 60
CAAGTTCAAC AAAACGCCTC AAGGCAAGGG GCTGGGCTAC GGGGAAGCAG ACTTGGCCCT 120
GTGCTAGAGA TGCGTGAAAC ACATCTGCAC ATCTGAGTGG CAGCACAGTT GAGGTTGTCC 180
TGCAACTCAG CCTGTCTCAC ACTGAGCATG GCACTGGGCC TAGGGACTCT GCTGTCTGGC 240
TGCTCCGTCC CCCAACCTCC CATCCCATTC CGTCACTGCC CAGCCTGACT GCCTTCTGCA 300
CGCCACAGCC AGGCTGCTCC CAGCCATTGC AATTGCTTCC TTCCCACCCC ACCTCAGCAC 360
CTGGCCCTAC CGGCCTCCTC ACTGGCCAGC CTGCCTCATT GCCTTCTCCA ATCCCTCCTG 420
CTTTTTTCTT TTCTTTCCTT TTTTTTTTTT TTTTTTTTTT TGCGACAGGG TCTCACTCTG 480
TCGCTCAGGC TAGAGTGCAG TGGCACCATT ATGGCTCACT GCAGCCTTGA TCTCCTGGTC 540
TCAAGAGATC TTCCTGCCTC AGCCTCCTGA GTAGCTGGGA CTACGAGTGC ACTCCACTAC 600
GCCGTTAATT TTTGCTTTTT TGTTTTCTTG TTTTTGTTTT GAGACAGAGT CTCGCTCTGT 660
CACCCAGGCT GGAGTGCAGT GGCACAATCT CGGCTCACTG CAACCTTCGC CTCCTGGGTT 720
CAAGCAATTC TCCTGCTTCA GCCTCCTGAG TAGCTGGGAT TATAGGCATG CACCACCACA 780
CCCAGCTAGT TTTTGTGTTT TTAGTAGAGA TGAGGTTTCA CCATGTTGGC CAGGCTGGTC 840
TCAAACTCCT GACTTCAAGT GATCCACCCA CCTCGACCTC CCAAAGTGCT GGGATTACAG 900
GCATGAGCCA CTGCACCCGG CCATTATTTT TTGTACAGAC GGGATCTCGC TATGTTGCCC 960
AGGCTGGTCT CACACTCCTG GCCTAGAGCG ATCCTCCTGC CTCAGTCTCC CAAAGCACTG 1020
GGATTCCAGG CATGAACCAC CATGCCTGAC CACTCCCATT ATTTCTAACA TGCAGATCTG 1080
AACACCCATT CACTCATTCC ACAAATACTT ATTGAACAAT TCCTATGTCC CCTGCAGAGT 1140
GGCTGGCTCT GAGGACACAG TACTGAATAA ATGAGACAGA ACTCCTTGCC ATGCAGAACC 1200
TGCCTCCTGA GGCCACATCC ACCAGCTCAC AGGCCTTGGA AGGCCTTCTG AGTGACTCCA 1260
CCTGGCACGT GCCATCCTTG GCTCCTCCCA GGGCGCCCTC CCACCTTATC TCCCATCGCT 1320
GCCCTTGATT CCAATACCCC GAGCCCAGCT GGCGCCCCTC ATGCCCTCTC TGCCTCCACG 1380
GGTTCAGGTG AGCTCACAGG CCAAGGCCCA GCTCAGCCAC CTCCTCCTCC ATGCGGCCTT 1440
CCTGATGTGC AGCTGCCGTG ACTACTCCTG TCTCTGGGGT TCTCTGGGAG CCTGTGTTTA 1500
GGGCCCAGTC TCTTCTTCCA GTGATTTATT TGCTAGCATG TTTATCTCTC CCCAAAGCTC 1560
TGAGCTTCTG GAGGCCAGGA CATGTCTTCC TTGTCTCTGC ATCGCCCACG TAGGCCACTT 1620
TGAAATGTTT GTTGAATGAG TCATCGAGTG AAGGAAGGAA CCCGCAGAGG AACGGTTGCA 1680
GAAACTTTGG GGGAGGCCTG GGCACCAAAG GCGAGGCGTG GTGGCGGAAA GCCGACACTA 1740
GAGGGCGACA GAGAGTAAGG GAAAAAATGC AGCCAGGACC AACAGGCTTG GAGCAGAGAG 1800
ATGCCTGGGC CAGGGCTCGT CCCAGCCTGG AAGCCCCAAG CCTTCGTCCT CCATGCCTGC 1860
CCTGGCTTCG TGGGGAAGGG GTGGGGAGCA TACCAGCCCC CCCCCCGCCC CACCCCGTCT 1920
GAACTCAGTC AGCCGACTGA ACTCTGCTCT ATACCCTGGG GAAAGGGAAG AATAGGACCA 1980
GGACGGCCGG CAGGAAAACA GGAAACTCCA GTCCCAGAGC AGCGGGCAGA AGACCGTCCC 2040
CAGGATGTGG GCACTTCTCG CCAGAGGGTC CTGAGCCTGG GGCGCACTCT TCTGGTTTGG 2100
GGTAAACTTG GTCCTCTCGT GGTCTCTCTC TCTTCAGATA GGGCCCAGGG GAGCCCCCAC 2160
TCCATACCAC GTTTTTCCTT CCAACACATA CAGCAGCCAG GAGGCCGGAC AGAGCTTTCC 2220
GGTTTCCTGT TTTCACAACT GTATTTTCCC CTTTCTCCTT AATCAGTTTC CTACAGCCCC 2280
AGACAGGGTG ACAGGCCACA GGGCACCTGC CCAGCTTGGC TGTCCCAGCC TGTCCCCCAT 2340
CCCCTCACCA CCCCCAACTT TTTTTTTTTT TTTTTTGAGA CAGAGTCTCG TTGTGTCACC 2400
CGGGCTGGAG TGCAGTGAGT GGTGCAATCT CAGCTCACTA CAACCCCCAC CTCCCAGGTT 2460
CAAGCAATTC TCAAGCTTCA GCCTCCTAAG AGCTGGGACT TTGGGTTTGC ACCACCATGC 2520
CCGGCTAATT TTTGTAGGTT TTTTTTTTTC TTTTGAGATG GAGTTTCACT CTTGTCGCCA 2580
GGCTGGAGTG CAATGGCACG ATCTCGGCTC ACTGCAACCT CCACCTCCCG GGTTAAAGTG 2640
ACTCTCCTGC CTCAGTCTCC TGAGTAGCTG AGATTACAGG TGTGCACCAC CACACCTGGC 2700
TAATTTTTGT ATTTTTAGTA GAGATGGGAT TTCACCATGT TGGCCAGGCT GGTCTCGAAC 2760
CCCTGACCTC AGGTGATCTG CCCACCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA 2820
GCCACTGCGC CTGGCCTAAT TTTTGTATTT TTAGTAGGAA CAGGGTTTCA CCATGTTGGC 2880
CAGGCTGGTC TCAAACTCCT GGCCTCAAGC AATCCACCTG CCTCAGCCTC CCAAAGCGCT 2940
GGGATTACAG GCATGAGCCA CCTCGTGCGG CCTGCCTGCC TTTTTTTGAG ACGTTCTAGA 3000
AGACCCCGGG CCTCCTGCCT 3020