EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-09355 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr17:48981160-48982470 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr17:48981187-48981201AGTCCCTGGGGAAG-6
Foxd3MA0041.1chr17:48981168-48981180AAACAAACAAAC-6.32
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_02991chr17:48980818-48981364Bladder
SE_02991chr17:48981621-48983308Bladder
SE_04178chr17:48981233-48983332Brain_Anterior_Caudate
SE_05235chr17:48980897-48982005Brain_Cingulate_Gyrus
SE_06067chr17:48981497-48983596Brain_Hippocampus_Middle
SE_07466chr17:48981344-48983162Brain_Hippocampus_Middle_150
SE_08899chr17:48982228-48982374Brain_Mid_Frontal_Lobe
SE_12167chr17:48980692-48983336CD3
SE_19619chr17:48979853-48984374CD4p_CD25-_Il17p_PMAstim_Th17
SE_23191chr17:48981481-48983372Colon_Crypt_1
SE_23784chr17:48981620-48983342Colon_Crypt_2
SE_24830chr17:48981426-48983406Colon_Crypt_3
SE_26011chr17:48979932-48984292Duodenum_Smooth_Muscle
SE_26691chr17:48979620-48983743Esophagus
SE_27621chr17:48979817-48984219Fetal_Intestine
SE_28540chr17:48979724-48984381Fetal_Intestine_Large
SE_29967chr17:48979940-48983528Fetal_Muscle
SE_31399chr17:48980105-48984402Gastric
SE_36690chr17:48980078-48983446HMEC
SE_41117chr17:48980937-48983480Left_Ventricle
SE_42844chr17:48981354-48983454Lung
SE_47468chr17:48980975-48981325Pancreas
SE_47468chr17:48981487-48983527Pancreas
SE_49193chr17:48981509-48983050Right_Atrium
SE_49713chr17:48981753-48983169Right_Ventricle
SE_50311chr17:48981438-48983399Sigmoid_Colon
SE_52502chr17:48981399-48983501Small_Intestine
SE_54412chr17:48981548-48983164Spleen
SE_54634chr17:48978631-48984793Stomach_Smooth_Muscle
SE_59738chr17:48979175-49044314Ly4
SE_65373chr17:48981580-48984477Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174898200048982200
Number: 1             
IDChromosomeStartEnd
GH17I050902chr174897976048984332
Enhancer Sequence
CACCAAAAAA ACAAACAAAC CCTGCTCAGT CCCTGGGGAA GAGAAAAGGC CAGGATATGG 60
AACAGGGAGG GAAGGGCTGC ATTCAAAATC CCGTCCTACC CATACATTGT AAAATGGTAC 120
AACCACTTTA GGAAACAGTT GGGTGGTTTC TTTAAAAGTG AAACATACAC TTACCATGTG 180
ACCCAGCAAT CCCTCTTCTA GTTACTAATG CGAGAGAAAT GAACACATGC ATCCACATGA 240
TGATTTATAT ACAAATGTTC ATAACTGCTT TACTCATAAT AGCTGCCAAC TGGAAACAAC 300
CCAGATGTCC AAACACAGGT GAATGGCTAC ACAAACTATA ACATATCCAT ATAATGGAAT 360
ATATTACTCT GCAATAACAA GGAAAGAACT ATGATAGACG CAACAATATG AACGAATCTT 420
GAAATCATTA GGCTGAGGGG GAAAAGTCAG AGGTAAGAGT AGAGTAGAAA CTGTATGGTA 480
ACGTATACAA AACATGCAAA TCTGATCTGT CATGACAGAA AGCAGATTGG TGCTTGCCTG 540
GGGCCAGGGA AGGGGCATGA CTGACTCAGA AGGGGCCACA GGGAACCTTT CAGGGTAACG 600
GAAATGTTCT CTACTTTGGT TATTGTGGTA GGTATGCAAA CATACAACAG TGCACCTAAA 660
ATGGGCACAT TTTGTTGTGC GTAAGTTAGA CCTCAACAAA GTTGACTTAA GAAATAATTC 720
CTTCCCGAGA GCCTGGCCTA CGAGGTGCGG GCAAGCAGAG AGGCCTCCCT CAAGGCACTG 780
GCGATACTGC CAAGCTGGAA AAACGGCTCG CTGGCAGCCT GGAAAAGGCC GTTCTCTGGC 840
TCTTGATCCT TAAAAGGCTG GAATTTCTGG CTGAACAAGA AGGCCTGGGC CCAGTCCCCA 900
GGGGGCAGCT TCTCCTCAGC TCTGGGCAGG GTGCCCGGCC ACCCCTCACA CAGGTGCTGG 960
CTTGCTGCCC AAACACAGGA CCAGGGGGCC TGGGCAGGCC CCCACAGCCC TGCTGGGGGA 1020
AGAGGAGGAG ACCAGCCCGT AGCCAGCCCA GCCTCAGCCC CAGCAGCCTG TGGCTGGCAG 1080
GGCCTCTGCC TACACAGCAA GCTCTCAGAG TGGGGGGATG GGAGCAGCGC CCAGGCACCC 1140
ACCCAGCTCC CCCAACCCAG AGTGTCACCG GGGACCTTTA CCCTGAATGG GGATGGTTTT 1200
AACAGCCCCT AGAGAGGGTC AGGGCATCTG TGACAGGACA GGGTCTGAGC CCCGGACTTT 1260
CACCTCTCAG CCCAGTGCCC TTTTCCCCGC AGCAGCCTAA GCTCCCAGTG 1310