EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-17304 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr17:48995350-48997450 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX2MA0600.2chr17:48997194-48997210CATTGCCATGGAAACC+6.15
RFX2MA0600.2chr17:48997194-48997210CATTGCCATGGAAACC-6.18
RFX5MA0510.2chr17:48997194-48997210CATTGCCATGGAAACC-6.1
RFX5MA0510.2chr17:48997194-48997210CATTGCCATGGAAACC+6.24
RREB1MA0073.1chr17:48996249-48996269GGGGTGGGGTGGGGTGGGGG-6.74
RREB1MA0073.1chr17:48996248-48996268TGGGGTGGGGTGGGGTGGGG-7.67
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_02991chr17:48994624-48997228Bladder
SE_03517chr17:48995128-48997800Brain_Angular_Gyrus
SE_04178chr17:48993971-48998112Brain_Anterior_Caudate
SE_05235chr17:48993417-48998834Brain_Cingulate_Gyrus
SE_06067chr17:48993102-48998709Brain_Hippocampus_Middle
SE_07466chr17:48993799-48998941Brain_Hippocampus_Middle_150
SE_08267chr17:48993505-48998192Brain_Inferior_Temporal_Lobe
SE_08899chr17:48996334-48997100Brain_Mid_Frontal_Lobe
SE_08899chr17:48997164-48997725Brain_Mid_Frontal_Lobe
SE_12167chr17:48995751-48997883CD3
SE_19619chr17:48992187-48997884CD4p_CD25-_Il17p_PMAstim_Th17
SE_23191chr17:48993461-48997830Colon_Crypt_1
SE_23784chr17:48993579-48997752Colon_Crypt_2
SE_24830chr17:48993475-48997727Colon_Crypt_3
SE_26011chr17:48995459-48999208Duodenum_Smooth_Muscle
SE_26691chr17:48991965-48997875Esophagus
SE_27621chr17:48994705-49002048Fetal_Intestine
SE_28540chr17:48994683-49002269Fetal_Intestine_Large
SE_29967chr17:48993411-48995672Fetal_Muscle
SE_29967chr17:48996231-48997810Fetal_Muscle
SE_31399chr17:48991729-48997856Gastric
SE_35088chr17:48996270-48997943HeLa
SE_37666chr17:48996166-48998175HSMMtube
SE_41117chr17:48994694-48997767Left_Ventricle
SE_42844chr17:48995090-48997815Lung
SE_47468chr17:48994886-48997790Pancreas
SE_49193chr17:48996258-48997806Right_Atrium
SE_49713chr17:48996488-48997655Right_Ventricle
SE_50311chr17:48993122-48997822Sigmoid_Colon
SE_52502chr17:48995428-48997845Small_Intestine
SE_54412chr17:48996674-48997693Spleen
SE_54634chr17:48995397-48999082Stomach_Smooth_Muscle
SE_57199chr17:48996702-48997718VACO_400
SE_59738chr17:48979175-49044314Ly4
SE_65373chr17:48993878-48999624Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr174899560048995887
chr174899694448997365
Number: 1             
IDChromosomeStartEnd
GH17I050914chr174899193349001980
Enhancer Sequence
AGGGGGTCCT TGGACCTCTA TCTCAGCAGG GACATTCCTC CTCCCCCCGC CTTCCAGACC 60
TCCTGCTCCA GATGCCTGGC TTCTCCAGGG CACCCCGATG GGTGGCTCTG CCACCCCAGG 120
ACACTGGACT GGGGCCACCC TTACAGAACC GGTTCGAAGC CAAACAATGG CACGTCACAG 180
TCCAGCTGAG CCGGAGGCCT CAGCAGGGTA AGTACAAGTG AGGCTGTGGC CAAGAGGGGC 240
ATAGGTGCCA GGGACTCAGA GGCGGGCGCG CGCAAGTGCC AGCAAGCCCT CACTGCCTAA 300
CATGGCAGCC CCATGGCTTC CTCTCTTCCC CGTGACCTGA CTGCAGCTTT GAGGACAGCA 360
CTTGCCCTCC CCTCCCAGGC AGCGGGCCCC TTCCCTGGCC CCAGAGGTGA AGGAGGGCGA 420
CTTCCCCAGG GAGAGGAAGC AGAATGACGG CCTGCAGCTT TCCTGCCGCG GGAGGGGAAC 480
TTCAGGTCAG AATGGCCGTC TCAACCTCAT GGAAGCCTCC CTCTGGACTG ACGAGTGACC 540
GCTGTTGTGG TGGGAGGTCC ACCTTCCCGC AAAGGGAGCC AAGAGCCCAG AGGGGTCACT 600
TGGGCCCAGG GAGGGTGGGA CACAGACGTC TGGGTGGAAG TTGGACAAAG TCTGGCAGAA 660
TGGGGCACCA GGGCACAGTA AGACCCTGGC TGGGACACTG AGTGGGGACA GTCCCCAGCA 720
ATTCCCTTGG AGATAAAGAG CCTGCGGCAG GTCCCAGATC CTGACAGAGG ACAGACAGGA 780
GGGGACAAGC TGGTGGTGGG GGTGAGCTGG CTAGGCAGAA AGCTCTGTGG ACACCTGAGG 840
CCTCCTCCTG GAATTGCCCC AAGCCATGTG GCTAAGGCCT AGGGAGACCC TCACCATGTG 900
GGGTGGGGTG GGGTGGGGGC CCCTAGCCAA AGCTGGGAAA AGGCAGAGCC TTCAGAGAGC 960
CTCCTAGGGA CAGCAGCAGA GAGGAAGCCT TCGAGGCCTT TCCAAGCTCC CCGCTGCCCG 1020
GCTCTCCTCC TGCCCAGCAC ACCGTGGGTG GACTCCAACC TACAGCTTCA CTGATCTCAG 1080
AAGGTCCCAC CCTCTCCCGC CTTGTGCTTC TGACTGTTTA TTTCCTGCAG AGGAGTCAGT 1140
GTTACTGCCA CTGAGAACAG AGATGGCTCC ACCCAGAGGG CCCACCCTTG GGGCACAGGG 1200
GACCCTTGCC CATACCCCCT GCACCCTGGC TCCATCCTAA TGCAGGGATA TGAGCTTGGG 1260
CCTGTGTCAC AGCTGCTTCC TGGGCCTCTG AATCCTCATC CTTGAGCTGA GGGTGTGAGA 1320
CCGGAAAATC CAAGCCACCA TCCAGCCCCA ATGTCTCCCC ATCCCATGAC TCTCTTCCCC 1380
AAATAACACA TCTCCCCAAA TACCTCTCCT CCTCCCCAGT GAGAGGAGGC GCAGGGGAGG 1440
TTGTTGGATA ACTGTGCCTT CTCCTCCCCG AATCCCAGCC TCTCCTTCTG GATCCCACAC 1500
CCAGGGGCCC AGCAGTCACG GGGCTCAGGG TGCTCCCCAG CCTTTACAGT TTACCCATCC 1560
CTGCACAGTA GCCATGATTT CATTTCCTCC TCACTGCAAG GTAAAGATCA TTAGTTCTCT 1620
TTTATAGGTG AAGAGACTTA GACTCAGACA GACCCTGTGT CTTGCTCAAA GTCACCTGGC 1680
CAGTCAGGGG TAGGGCTGGG TTTCGAACCC AGGGGCAGGC CCTCTCCGCC CCCCGGCATC 1740
GGTGCAGAGC CCTGGGTCGC CCTCCTCCAA GGTCGTTGTG GTGTGAACAG CCAGGCGCCT 1800
TCATGCAGGG CCTGACTGCA GCCGCCAGAG CCTGGTGATG TCAGCATTGC CATGGAAACC 1860
CTTCCCCGGG CGTCGGGCAG GACCAGCCTC CCCAGCGCAG TTTCCCTTTG TGTGGACTTT 1920
GCAATGCGTT GCCAAGGCAG TGGGGCCTGC TGGGCGGGTT GGCATGGGGT GGGGAAGGCA 1980
GACAAAAACC CACACTGCAA CTGGCAGCTC ACAACAGGGC CCACGGTGCT TGTGGGAGGG 2040
AGGGGCTGCA GGCTGGTGGC CTAAGGCGTG AGAGTCGGTG GGCAGGGGGT TACCCACACA 2100