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

TagContent
EnhancerAtlas ID
HS108-03951 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:206747190-206750080 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr1:206749069-206749080ACAGATAAGGA-6.14
RESTMA0138.2chr1:206747997-206748018TTTGGGACAATGGACAGTGCC+6.23
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_09327chr1:206745188-206758382CD14
SE_10603chr1:206747310-206756416CD19_Primary
SE_11004chr1:206727079-206757887CD20
SE_11917chr1:206746090-206750296CD3
SE_14503chr1:206746009-206758997CD4_Memory_Primary_7pool
SE_16490chr1:206747976-206750712CD4_Naive_Primary_8pool
SE_16959chr1:206747363-206748061CD4p_CD225int_CD127p_Tmem
SE_16959chr1:206748089-206757504CD4p_CD225int_CD127p_Tmem
SE_17411chr1:206724289-206760065CD4p_CD25-_CD45RAp_Naive
SE_17843chr1:206723887-206758306CD4p_CD25-_CD45ROp_Memory
SE_18269chr1:206723684-206769868CD4p_CD25-_Il17-_PMAstim_Th
SE_19128chr1:206746389-206766399CD4p_CD25-_Il17p_PMAstim_Th17
SE_20034chr1:206746357-206757932CD56
SE_20823chr1:206746904-206757454CD8_Memory_7pool
SE_22080chr1:206746077-206757652CD8_Naive_8pool
SE_22390chr1:206744356-206757869CD8_primiary
SE_25703chr1:206746359-206750220DND41
SE_27304chr1:206748233-206749980Esophagus
SE_31229chr1:206747597-206750097Fetal_Thymus
SE_39708chr1:206748495-206749981Jurkat
SE_50667chr1:206747343-206754765Sigmoid_Colon
SE_53261chr1:206746644-206756568Small_Intestine
SE_53552chr1:206746429-206757806Spleen
SE_55221chr1:206747302-206748199Thymus
SE_55221chr1:206748265-206748685Thymus
SE_55221chr1:206748689-206750305Thymus
SE_59167chr1:206727342-206757447Ly3
SE_62534chr1:206724532-206763666Tonsil
SE_65624chr1:206747328-206748146Pancreatic_islets
SE_65624chr1:206748409-206749787Pancreatic_islets
SE_66615chr1:206748495-206749981Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1206748926206749451
chr1206748515206748888
Number: 1             
IDChromosomeStartEnd
GH01I206573chr1206746529206757654
Enhancer Sequence
TCGGAGTCTT AGTGAGGTGG ACTTGATCAA GTTCACAGAA GACCAAGGGC ATGGCCAGCA 60
CAGGCCACCT GTGGCCCAGC GTGCAAGGCA GCATGGTCTA ATGGTGAAGA GTAACAGCAT 120
CTTTCTTGTT ATTTAGGGGA TTAAATGAGA TCAGGACCTT GAACCCTTCA GGGCAGTGCC 180
TGACTACTGT CGGTTTTTAA TATTATAATG AGGCTCTGCA GGGGCTTGAA CTTAGGTCCC 240
TGTAAGGGAG CTACTGTTCC CTGGTATGAC CCACTCTAGC TGAGCTGTGC AGAGACTGAG 300
ATGGTCACCT CAAAGAGCAG GGGACCCCGT GTCCAGACTC TGGGGCATGC TGGCAACCTG 360
AGGAGTCTGC GGGAGTGGCC TGATCTGTGC TGCTTGAGGC TTTTTGTCCC AGATCACACT 420
GTACTTGCTC TGGTGTGCCA CAGCGCATCC ATCTCTGTCT TCCCTTCTCA GGTCACCTGC 480
AGACTCCCAA GGACAGGGTC ACATCCCATC TGCGTCATCT CTCAAGGTGC CTTTCACGAT 540
CCTCACCCAT AGGCAGTTCA TTCAGTTACT ACTGGCGGAC TGTTGACATT GACCATCTGC 600
TCTACGTTTT TGTCTTTGGA GACTTGAGTC TCTTTCCATT CTCAACCTCC ACCCGCCACC 660
TCTTTTTTCC CTCTGCTCTG TTAATACACC CTACCAGAGC TGCTCAAATT CCACATGGAG 720
CAGAAGCTCC ATGATAAAGC CCCTTCCCTG CTCTGCTGCA AATAACCTAT TAGGGAACAC 780
AGTTAAGGAG TTCCCAACCC TTTTAATTTT GGGACAATGG ACAGTGCCAT AGAGGGACCT 840
GTGGAAATCA ACCCCTTCAC TGCTGTGGTG GGTCTGTGGA GTCCATTTCA GAACACAGGC 900
CTTCGAAGAC CTGGGAGGGG GCCCTGCAGT AAGGCCCCAT AGGGATTCCT CTTTCTCATT 960
TGGTTGAGAC CATCACAAAG GGACCAATGA CTTTTTTTTT TTTTTTTTTT TTTTGAGATG 1020
GAGTCTCGCT CTGTCATCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC AATGCAACCT 1080
CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG GGATTACAGG 1140
CGCACGGATA ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA 1200
TTATGTTGCC CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT 1260
GAGCAGGGTA TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT 1320
TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA 1380
GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT 1440
GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA 1500
GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT 1560
GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT 1620
GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT 1680
TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG 1740
AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA 1800
ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC 1860
AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC 1920
CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG 1980
CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC 2040
TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC 2100
TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC 2160
ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA 2220
AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA 2280
ACAATCATTA AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT 2340
CTGAAATCAC CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG 2400
ATCTGTGACG ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT 2460
GGGGCTGGTG TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA 2520
TCCCTACCCC AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT 2580
CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG 2640
TTACAAAGGC CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG GAAGTATGAT 2700
TCAGGAGAAA GAGAGACCAG GACAAAACTG TGATTACCTT TCTCCATGTG GGAATCAAAA 2760
TGCCAGGGAT CTGGTACATT AAGAGAGCAG AGGATGGAGA GATGGCTATA GACTGGAGAA 2820
ATTGCATTGG GAAACTACAT AGAGAAGGTG GAACTAGGGC TAATAGTGTT CTAGGCAGGA 2880
GACTCTGCAC 2890