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

TagContent
EnhancerAtlas ID
HS059-03916 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr1:206747200-206750240 
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: 3             
ChromosomeStartEnd
chr1206748926206749451
chr1206748306206750240
chr1206748515206748888
Number: 1             
IDChromosomeStartEnd
GH01I206573chr1206746529206757654
Enhancer Sequence
AGTGAGGTGG ACTTGATCAA GTTCACAGAA GACCAAGGGC ATGGCCAGCA CAGGCCACCT 60
GTGGCCCAGC GTGCAAGGCA GCATGGTCTA ATGGTGAAGA GTAACAGCAT CTTTCTTGTT 120
ATTTAGGGGA TTAAATGAGA TCAGGACCTT GAACCCTTCA GGGCAGTGCC TGACTACTGT 180
CGGTTTTTAA TATTATAATG AGGCTCTGCA GGGGCTTGAA CTTAGGTCCC TGTAAGGGAG 240
CTACTGTTCC CTGGTATGAC CCACTCTAGC TGAGCTGTGC AGAGACTGAG ATGGTCACCT 300
CAAAGAGCAG GGGACCCCGT GTCCAGACTC TGGGGCATGC TGGCAACCTG AGGAGTCTGC 360
GGGAGTGGCC TGATCTGTGC TGCTTGAGGC TTTTTGTCCC AGATCACACT GTACTTGCTC 420
TGGTGTGCCA CAGCGCATCC ATCTCTGTCT TCCCTTCTCA GGTCACCTGC AGACTCCCAA 480
GGACAGGGTC ACATCCCATC TGCGTCATCT CTCAAGGTGC CTTTCACGAT CCTCACCCAT 540
AGGCAGTTCA TTCAGTTACT ACTGGCGGAC TGTTGACATT GACCATCTGC TCTACGTTTT 600
TGTCTTTGGA GACTTGAGTC TCTTTCCATT CTCAACCTCC ACCCGCCACC TCTTTTTTCC 660
CTCTGCTCTG TTAATACACC CTACCAGAGC TGCTCAAATT CCACATGGAG CAGAAGCTCC 720
ATGATAAAGC CCCTTCCCTG CTCTGCTGCA AATAACCTAT TAGGGAACAC AGTTAAGGAG 780
TTCCCAACCC TTTTAATTTT GGGACAATGG ACAGTGCCAT AGAGGGACCT GTGGAAATCA 840
ACCCCTTCAC TGCTGTGGTG GGTCTGTGGA GTCCATTTCA GAACACAGGC CTTCGAAGAC 900
CTGGGAGGGG GCCCTGCAGT AAGGCCCCAT AGGGATTCCT CTTTCTCATT TGGTTGAGAC 960
CATCACAAAG GGACCAATGA CTTTTTTTTT TTTTTTTTTT TTTTGAGATG GAGTCTCGCT 1020
CTGTCATCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC AATGCAACCT CTGCCTCCCA 1080
GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG GGATTACAGG CGCACGGATA 1140
ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA TTATGTTGCC 1200
CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT GAGCAGGGTA 1260
TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT TCCCATCTAG 1320
GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA GATGGACATT 1380
CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT GGCTTCCTTC 1440
CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA GGAAATGTGG 1500
CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT GAGTTGTGTG 1560
TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT GACAATAGAG 1620
AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT TTGTGCTCCT 1680
TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG AGGCCCCCAT 1740
CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA ACACCACCCT 1800
ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC AGTATCACTT 1860
CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC CCAGACGTCA 1920
CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG CTGAGCCACA 1980
CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC TCAGGGTGCA 2040
GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC TGAGACTCCC 2100
CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC ACCTACTTAA 2160
AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA AACTAATGTC 2220
TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA ACAATCATTA 2280
AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT CTGAAATCAC 2340
CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG ATCTGTGACG 2400
ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT GGGGCTGGTG 2460
TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA TCCCTACCCC 2520
AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT CCAAGGAAGT 2580
GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG TTACAAAGGC 2640
CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG GAAGTATGAT TCAGGAGAAA 2700
GAGAGACCAG GACAAAACTG TGATTACCTT TCTCCATGTG GGAATCAAAA TGCCAGGGAT 2760
CTGGTACATT AAGAGAGCAG AGGATGGAGA GATGGCTATA GACTGGAGAA ATTGCATTGG 2820
GAAACTACAT AGAGAAGGTG GAACTAGGGC TAATAGTGTT CTAGGCAGGA GACTCTGCAC 2880
AAACAACAGC ATAGAGCAAA CTACTGCACA TGGCCAGGTT CCATAAATAA AGTTTGTTTT 2940
GTTTTTGAGA CAGGGTCTTG CTCTGTCACC TAGGCTGGAG TGCAGTGGCA CAATCACGGC 3000
TCACTGCAGC CTTGAACTCC TGGGGGCTCA GGTCATTCTC 3040