EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS149-00963 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr5:150477220-150480260 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17728338chr5150478318hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:150479175-150479193AGAAGAAAGGAAGTAAAG+6.04
IRF1MA0050.2chr5:150477986-150478007TTCTGCTTTCTCTTTCCTTTT+7.94
IRF2MA0051.1chr5:150477985-150478003CTTCTGCTTTCTCTTTCC-6.11
SPI1MA0080.4chr5:150479988-150480002CAAAAGAGGAAGTT+6.89
SPICMA0687.1chr5:150479988-150480002CAAAAGAGGAAGTT+6.45
ZNF263MA0528.1chr5:150479870-150479891GGGGGAGGGAAGGCAGAGGAA+6.28
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00624chr5:150471795-150491225Adipose_Nuclei
SE_09226chr5:150470896-150478712CD14
SE_13605chr5:150476429-150479236CD34_Primary_RO01536
SE_13605chr5:150479692-150481778CD34_Primary_RO01536
SE_15204chr5:150476445-150482207CD4_Memory_Primary_7pool
SE_17941chr5:150476396-150479537CD4p_CD25-_CD45ROp_Memory
SE_18317chr5:150472170-150479647CD4p_CD25-_Il17-_PMAstim_Th
SE_19111chr5:150477297-150478440CD4p_CD25-_Il17p_PMAstim_Th17
SE_23141chr5:150479614-150481837Colon_Crypt_1
SE_23836chr5:150479718-150480276Colon_Crypt_2
SE_25002chr5:150479722-150481848Colon_Crypt_3
SE_25989chr5:150479810-150481734Duodenum_Smooth_Muscle
SE_28253chr5:150479579-150480853Fetal_Intestine
SE_31853chr5:150479541-150481961Gastric
SE_32472chr5:150476410-150478853GM12878
SE_37013chr5:150471038-150478454HSMMtube
SE_40909chr5:150479685-150481833Left_Ventricle
SE_42116chr5:150477374-150479546Lung
SE_42116chr5:150479613-150481867Lung
SE_48252chr5:150479727-150481787Psoas_Muscle
SE_48796chr5:150479695-150481767Right_Atrium
SE_50074chr5:150472125-150478957Sigmoid_Colon
SE_50074chr5:150479620-150481888Sigmoid_Colon
SE_51316chr5:150479136-150480642Skeletal_Muscle
SE_52353chr5:150472070-150481988Small_Intestine
SE_53309chr5:150472028-150479367Spleen
SE_53309chr5:150479600-150481788Spleen
SE_59083chr5:150437761-150478457Ly3
SE_60748chr5:150431201-150478526DHL6
SE_62297chr5:150437930-150538770Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5150477506150477962
Number: 1             
IDChromosomeStartEnd
GH05I151091chr5150471363150481994
Enhancer Sequence
CTGGAGTGCA ATGTCACGAT CATGGCTCAC TGCAACCTCC GCAACCTGGG CTCAAGCGAT 60
CCTCCCACCT CAGCCTCTCG AGACTGCAGG CATACACCAC TACCTCCAGC ATTTTTTTTT 120
CCTATTTTTT GTAGAGACGG GGTTTTGCTA CACACAGGCT GGTCTTGAAC TGGGCTCAAG 180
CGATCTGCCC ACTTTGGCCT CCCAAAGTGC TGGGGTTACA GGCACGGGCC ACGGCACCTG 240
GCCATAGGGA AACTTTAAAC AGCCAGCGGT TCCCACACCA CCGCCACGGG CAGGAGGTTG 300
AGTGGCAATT CCTAAATAGC TGCTCTCTGC TCAGGTTAAA AGGGCACCCC CCCTCCCAAT 360
GGGCAACTTC CTTCGGGTAT TTCCTAGTGG CCCCAAAGAC CAAGATTGGC CCATCCCAGT 420
TCAGAGCTTG TAACAGTTTG CCCTAAAGGG AAAATGCAAG GCTCAAGGCA GGAGGGGGAG 480
CAGTGAGGAG CTAGAGAGTA TTGAAGCCCA CCTCCACAGG TGACGACAAA AGGAGAAAAC 540
ACAGGGTGCT TCTAAAAGCA CCGGCCCTGG CCGGGATGGC AATTCCAGTT CTGTCTGCTG 600
CTAGCTTGCT ATGTACCCTG GGCCAGTTGC TTCCTCTCTG TGGAAGTGAC AGTTGTTTCA 660
TCTGCAAGTG AGGGAGGGAG GTGAGAATTT CTGAGGGCCC CTTCTACCCT TAGAACATCA 720
CAGCCAGCCT CCCTTTCTCC CACTTTGAGA CAGCAGCGGT TTGGGCTTCT GCTTTCTCTT 780
TCCTTTTAGT TTTAAATTAG CCCCCATCGC TTCTCCCGAT TAAACTTTGG CCACAGAAGC 840
AATCTCCAGT GTCATTTTGG AGAGAGCTGA GCAGGAGGGA CACTCAGTGG AAGCTCCTTA 900
AGCACCAGAA CCACATTGGT TTGTATGTTT TGCACCTAGC ACGTGGCATG GAACATAGGA 960
GCCACTCATT AAGTGTAAAC TGCATGCATG CATGAATGGG GTGCTCTGGT TCAGAACAGT 1020
GGCTACTCTC CTCCTCTGCT AAAACTCCAA GAAAAAAATG TGGTTTGTTC AGCTGGCACC 1080
GAGCTCTTAG TAGGACCGTT GCAAAAGGCT CCCGAATGGC ACCCTGCCTT CCTACATTTG 1140
TCCTCAGAGC ATAGCTAGAC GCACACCTTC CCCACTCAAG AACTCCAAAG GCTTCCCCTA 1200
GGTTATCAGA GAAAATCCTG ACATTTAAAG TCCTCCTTAA TTGGAGACAA ACTGTCACTT 1260
CTCATCTTGT CTACCTCACC TCACAAACTC TTAGGGTTTC CTTCCTGCTA CCGACCAGTA 1320
CCAGAATGCA ACTACCTTAA CTGAAAATTA TGTGGAAAAT GCATGCTGAG GCATTAGGGA 1380
GGCATCAGAC AGCTACTGCC CGATTTTAGC TGTCCTCATT CCTGGTTTCT AGGCCTCCTC 1440
TTCTGTGTTC CCCTCAGCTC CATGGGCTCT CCTCACTTCT ATTCCCTGAT TCCACTCTTC 1500
TTTCCTTTCT GCCCCAAGCC CATTTCCCTC AGTATATATT TTAAGGCACT TTTCTTTTTG 1560
GGTTCAAATG CCTTTGTGAT CTGCAGCTGA CGGACTTCAT GAAATCAAAG CCATAAAGCA 1620
TCATGGGCTC CACCTTTCAG CCCCTACAAC TGAGCCTGGT TCGGGGCAGG TAGTGAGACT 1680
GACTCCGAGC CAGGCACGCA CCCTGCCAAG CACCTCCACG TGGTGCCTCC TTTTATTCCC 1740
ACAAGGCTAC AGGATAGGTG GAATTGGAAT GAGGAGCCCT GTTTTACAGA GAAGGAAACC 1800
GAAGCTCCTG TGCTGACGGT CAGTTAGTTA CAAAGGTCTT AATCCAAAAC TCTGAACCAT 1860
TTTGTTAATT TATCTTTCAG TAACAGTTCA ATTAAGTTAG ACAAATATCC CAAAAAGCTC 1920
TTAGCTGGCC CTCAAGGCAC TTGAGTTCAC AGCCCAGAAG AAAGGAAGTA AAGACACGGT 1980
AAGGTAACTT TTCTTTGTTT CAGACTCATT ATGTCAGAGA TTAAGAGAGA GCTCTTCAAA 2040
ATTGTTGGAT CCAACCCCCC ACTATAAAGT TGGAGTAACT GAGGCCCAGT GAGGGCAATG 2100
GCTGGTCTGA GGTCACAAGT GAGGGAGGGA CGAGACCAGA CTCTCTCACC TGCCTGTTGC 2160
TGTCTTCACA GCTATGAAAA CAAACACATG CGCCGCGCAC GGTGGCTCAC GCCTGTAATC 2220
CCAGCACTTT GGGAGGCCAA GGCGGGTGGA TCACCTGAGA TCAGGAGTTC GAGACCAGCC 2280
TGACCAACAT GGAGAAACTC CATCTCTATT AAAAATACAA AATTAGCCAG GTGTGGTAGC 2340
ACATGTCTGT AATCCCAGCT ACTCGGGAAG CTGAGGCAGG AGAATCGCTT GAACCCGGGA 2400
GGCAGAGGTG GCAGTGAGCC AAATTCATGC CATTGCACTC CAGCCTGGGC AACAAGAGCG 2460
AAAGTCCATC TCAAAAAAAA AAAAAAAGAA GAAAAAGAAA AGAAAGAAAA GAAAACAAAC 2520
ACGCGCTAAC CTGCAATAAA CTAGTCTGGT CAGCCAGGGT AGGGAGAAGT GCCCTTTGGC 2580
CAGCAGCCAG CCCCATGCCA TGGTCACTGG ACAATCTTAG ACCAAAGCCA CAGACCAGAA 2640
GTAGGGCAGC GGGGGAGGGA AGGCAGAGGA ACTGCAGTTG CGCCTACTTG CTTATCAGTG 2700
ACCTGCATGA AGGAAACTTT CCATGCACCT CTCCAGATCA AGATCACATC GGGCACCCTT 2760
GCATAGTTCA AAAGAGGAAG TTTGGGCTTG GTTGAAATGG ATGAAGAGCA TACAGAAATG 2820
TCCAGACAGC GAGAGGGGAT GAGGGGGAAC CTGAGGCCCG GAGCAGGGCT GGGCCAGCCT 2880
TCCCAGGCTT GCTGCAAACT CAGATTCTCC TGTGCGCTTC CCGGGAAACA CCTTGCAAGA 2940
ATTTAAAGAC GTAACTCGCT CCTGGACAGA CTTTACAACC TCAAGCTCTA ATGAGGAAAA 3000
TCCAGGCTGC AGGCTCTAGG TAGAAGACAG AGGCCCTCAC 3040