EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-33089 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr5:150474540-150476150 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr5:150475985-150476006TTTTTCTTTCTTTTTTTGTTT+6.45
IRF1MA0050.2chr5:150475979-150476000TTTTTCTTTTTCTTTCTTTTT+6.68
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00624chr5:150471795-150491225Adipose_Nuclei
SE_01392chr5:150474915-150475951Adrenal_Gland
SE_09226chr5:150470896-150478712CD14
SE_13605chr5:150472133-150475716CD34_Primary_RO01536
SE_15204chr5:150473507-150475443CD4_Memory_Primary_7pool
SE_17941chr5:150472544-150476151CD4p_CD25-_CD45ROp_Memory
SE_18317chr5:150472170-150479647CD4p_CD25-_Il17-_PMAstim_Th
SE_19111chr5:150472583-150477050CD4p_CD25-_Il17p_PMAstim_Th17
SE_23141chr5:150472937-150476212Colon_Crypt_1
SE_23836chr5:150473278-150476109Colon_Crypt_2
SE_25002chr5:150472818-150476158Colon_Crypt_3
SE_25989chr5:150472379-150476998Duodenum_Smooth_Muscle
SE_27123chr5:150473282-150474873Esophagus
SE_27123chr5:150474877-150475844Esophagus
SE_28253chr5:150472024-150476840Fetal_Intestine
SE_30354chr5:150474570-150476050Fetal_Muscle
SE_31853chr5:150473207-150476185Gastric
SE_32472chr5:150472642-150476061GM12878
SE_35096chr5:150471270-150476106HeLa
SE_36009chr5:150471186-150475172HMEC
SE_37013chr5:150471038-150478454HSMMtube
SE_40909chr5:150472946-150476168Left_Ventricle
SE_42116chr5:150472186-150476175Lung
SE_47695chr5:150474446-150475973Pancreas
SE_48252chr5:150472467-150476126Psoas_Muscle
SE_48796chr5:150473099-150476102Right_Atrium
SE_50074chr5:150472125-150478957Sigmoid_Colon
SE_51316chr5:150472516-150476173Skeletal_Muscle
SE_51803chr5:150471359-150476076Skeletal_Muscle_Myoblast
SE_52353chr5:150472070-150481988Small_Intestine
SE_53309chr5:150472028-150479367Spleen
SE_56023chr5:150472010-150476028u87
SE_57972chr5:150474420-150476084VACO_9m
SE_58791chr5:150431451-150475486Ly1
SE_59083chr5:150437761-150478457Ly3
SE_60748chr5:150431201-150478526DHL6
SE_61344chr5:150438255-150475360HBL1
SE_62297chr5:150437930-150538770Tonsil
SE_63588chr5:150471359-150476164HSMM
SE_67545chr5:150472010-150476028u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5150474739150475397
Number: 1             
IDChromosomeStartEnd
GH05I151091chr5150471363150481994
Enhancer Sequence
GGAGCTAGTC TTGTCTCCCA GAATAGGATG CCAAGTAGGA TCAGAGTTCA AGTCAGGGCT 60
GTTGGGCTCG AAGTCTGCCC TCCACACAGC CTGGTTGGTT GTCCTCCTCT GATGGGCTTA 120
CACAACAACA AGCAGACTCC TGATTTCTGG AGGTGTGTGG GGCACACTAA GGCTATGCAC 180
TAAGAAAAGT GTGAGTGTGC ACATGCCCCA GTGTGTGTGA AGAACAAGTT AGGATACATA 240
TGCGAGGTGT TTCCCACGTG CACAGCAACA CACACACACA CACACACACA CACATAATGT 300
CTGTATTTTT GGTTGTTATC AGCAAACTAA AAAAAAATTA TTTTCTCTGT ATGGTCAACA 360
ATGTGTGTCT CTGTATGTGT TACCAGCAGA ATACCTTACA CTCCTTTGTA TTACCAGCAA 420
TGTGTTTCTC ATTCTACTGT GTGCTCTGTG GGTATGGCTG GCAGTGACTG TAATTCTGTG 480
TGACAAGCAG TATTTACGGG CCTTGAGTGG ATAGCAGGCA CATGGGAAAG TGGGGGAAGG 540
AAATGTCAGT TCCCCACCCT CCCTACTTTC CTTTCAGGCC CTCCCAGGTC AAGGTCCATG 600
GCCTTCAAGA CGGCCAGGGA GGGGTTCTGC CTGCAGCTGG CAGCACAACA GGCAGATGGT 660
GGTAGTTGGG AGGAAGGGGT GGGGCCATCC CACAGAAGGA AATGCATGTT CTGGAAATTT 720
TAACAGCTGG GCCTGTTTGT GTGGTGGGGG GACATTCCCA GACAGCTCTT GTTTAGGGTT 780
TTGTCAGTCC TTACCTAGCT GAGAGGAGGG CAGTGGGACA GCCTACATCA GGGACCTCTG 840
TCCTCATGTC CTTCTCTGAG TTCTTAGGGA ATGGAACTTG GCTTCACATC TGCTTCCTCC 900
CCGCTCACTC CCCATGGCAC TTTAGGGCCC TTTTCCCTGT TTTCTCGCTC CCCAGTGTCC 960
TTCTCTTTTC TCCATCTCTG CATCCTCTGT GCTGGCTTGT GTCCTCATCC CCCCGACACC 1020
TAGGGACCCC AGCTGCTGGT CCTGTCTCCT CCATGCTGGT CCCTGGGGAT ATCTTTTCTA 1080
AAGGACATCT CTAATCATAT AATCTCCCTC CCTAGCACAT TCAGGGGCTA GCCAGTGCCT 1140
GGAGGATAAA GTCCATACTC TTCAGCCTGG ACTCAGTGAC CTTCCCAGAG GGCGTCCTCG 1200
CACAGCGGGT GACGGGCCCC AGCACTCCCA CACACCTCTC CTTTCCCAGC TCTGCGCCTT 1260
TGCTTCAGCC ATTGCCTCTG CCTGGACACC CCTCCCTCCT TCAGTAGTTT CTAATGTAAG 1320
AGCTTCTCTA ACCATCTGCT GAGGTGCTCT CAAGTGTCCC GTTCTCCAAG GAGCCTTTGT 1380
TAGTCCTCCC TGTGGTTAAT TCATCGCTTC TGCACTCAGT GTCCCTTGCT TGGTTGAGAT 1440
TTTTCTTTTT CTTTCTTTTT TTGTTTTAAG ACAGTTTTGC TCTTGTCAAT CAGGCTGCAG 1500
TGCAGTGGTG TGATCTTGGC TCACCGTAAC CACCGCCTCC TGGGTTCAAG TGATTCTCCT 1560
GCCTCGGCAT CCCAAGTAGC TGTGATTACA GGTGCCCGCC ACCGCAACTC 1610