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

TagContent
EnhancerAtlas ID
HS105-74038 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr7:75920260-75922040 
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_00909chr7:75920271-75921957Adrenal_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_09135chr7:75920406-75920703Brain_Mid_Frontal_Lobe
SE_09135chr7:75920782-75920964Brain_Mid_Frontal_Lobe
SE_09135chr7:75921403-75921620Brain_Mid_Frontal_Lobe
SE_24584chr7:75921111-75921759Colon_Crypt_2
SE_26462chr7:75920316-75925507Duodenum_Smooth_Muscle
SE_26581chr7:75920201-75922116Esophagus
SE_29613chr7:75920891-75922015Fetal_Muscle
SE_31739chr7:75920277-75921989Gastric
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
CCAAAGTGCT GGGATTACAG GCATGAGCCA CTGCACCCGG CCATTATTTT TTGTACAGAC 60
GGGATCTCGC TATGTTGCCC AGGCTGGTCT CACACTCCTG GCCTAGAGCG ATCCTCCTGC 120
CTCAGTCTCC CAAAGCACTG GGATTCCAGG CATGAACCAC CATGCCTGAC CACTCCCATT 180
ATTTCTAACA TGCAGATCTG AACACCCATT CACTCATTCC ACAAATACTT ATTGAACAAT 240
TCCTATGTCC CCTGCAGAGT GGCTGGCTCT GAGGACACAG TACTGAATAA ATGAGACAGA 300
ACTCCTTGCC ATGCAGAACC TGCCTCCTGA GGCCACATCC ACCAGCTCAC AGGCCTTGGA 360
AGGCCTTCTG AGTGACTCCA CCTGGCACGT GCCATCCTTG GCTCCTCCCA GGGCGCCCTC 420
CCACCTTATC TCCCATCGCT GCCCTTGATT CCAATACCCC GAGCCCAGCT GGCGCCCCTC 480
ATGCCCTCTC TGCCTCCACG GGTTCAGGTG AGCTCACAGG CCAAGGCCCA GCTCAGCCAC 540
CTCCTCCTCC ATGCGGCCTT CCTGATGTGC AGCTGCCGTG ACTACTCCTG TCTCTGGGGT 600
TCTCTGGGAG CCTGTGTTTA GGGCCCAGTC TCTTCTTCCA GTGATTTATT TGCTAGCATG 660
TTTATCTCTC CCCAAAGCTC TGAGCTTCTG GAGGCCAGGA CATGTCTTCC TTGTCTCTGC 720
ATCGCCCACG TAGGCCACTT TGAAATGTTT GTTGAATGAG TCATCGAGTG AAGGAAGGAA 780
CCCGCAGAGG AACGGTTGCA GAAACTTTGG GGGAGGCCTG GGCACCAAAG GCGAGGCGTG 840
GTGGCGGAAA GCCGACACTA GAGGGCGACA GAGAGTAAGG GAAAAAATGC AGCCAGGACC 900
AACAGGCTTG GAGCAGAGAG ATGCCTGGGC CAGGGCTCGT CCCAGCCTGG AAGCCCCAAG 960
CCTTCGTCCT CCATGCCTGC CCTGGCTTCG TGGGGAAGGG GTGGGGAGCA TACCAGCCCC 1020
CCCCCCGCCC CACCCCGTCT GAACTCAGTC AGCCGACTGA ACTCTGCTCT ATACCCTGGG 1080
GAAAGGGAAG AATAGGACCA GGACGGCCGG CAGGAAAACA GGAAACTCCA GTCCCAGAGC 1140
AGCGGGCAGA AGACCGTCCC CAGGATGTGG GCACTTCTCG CCAGAGGGTC CTGAGCCTGG 1200
GGCGCACTCT TCTGGTTTGG GGTAAACTTG GTCCTCTCGT GGTCTCTCTC TCTTCAGATA 1260
GGGCCCAGGG GAGCCCCCAC TCCATACCAC GTTTTTCCTT CCAACACATA CAGCAGCCAG 1320
GAGGCCGGAC AGAGCTTTCC GGTTTCCTGT TTTCACAACT GTATTTTCCC CTTTCTCCTT 1380
AATCAGTTTC CTACAGCCCC AGACAGGGTG ACAGGCCACA GGGCACCTGC CCAGCTTGGC 1440
TGTCCCAGCC TGTCCCCCAT CCCCTCACCA CCCCCAACTT TTTTTTTTTT TTTTTTGAGA 1500
CAGAGTCTCG TTGTGTCACC CGGGCTGGAG TGCAGTGAGT GGTGCAATCT CAGCTCACTA 1560
CAACCCCCAC CTCCCAGGTT CAAGCAATTC TCAAGCTTCA GCCTCCTAAG AGCTGGGACT 1620
TTGGGTTTGC ACCACCATGC CCGGCTAATT TTTGTAGGTT TTTTTTTTTC TTTTGAGATG 1680
GAGTTTCACT CTTGTCGCCA GGCTGGAGTG CAATGGCACG ATCTCGGCTC ACTGCAACCT 1740
CCACCTCCCG GGTTAAAGTG ACTCTCCTGC CTCAGTCTCC 1780