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

TagContent
EnhancerAtlas ID
HS029-01291 
Organism
Homo sapiens 
Tissue/cell
CUTLL1 
Coordinate
chr1:206746950-206750140 
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
AGGCATAGAG AAGTAGTAGC AGTGGATGTA AGTCATTAAA GAGCTTCAGT CTAGTTGGGA 60
AGAAGACCCG AGATGGATGG TCTACTTGGA AGTTAATATA AGTAGCCAGG CGTAGTGGCT 120
CACGCCTGTA ATCCCAGCAT TTTGGGAGGC CAAAGCGGGA GGATCACTTG AGGCCAGGAG 180
TTTGAGACCA GCCTGGGCAA TATAGTGAGA GCCCCATCTC TTAAAAAAAC AAAATAGAAA 240
TCGGAGTCTT AGTGAGGTGG ACTTGATCAA GTTCACAGAA GACCAAGGGC ATGGCCAGCA 300
CAGGCCACCT GTGGCCCAGC GTGCAAGGCA GCATGGTCTA ATGGTGAAGA GTAACAGCAT 360
CTTTCTTGTT ATTTAGGGGA TTAAATGAGA TCAGGACCTT GAACCCTTCA GGGCAGTGCC 420
TGACTACTGT CGGTTTTTAA TATTATAATG AGGCTCTGCA GGGGCTTGAA CTTAGGTCCC 480
TGTAAGGGAG CTACTGTTCC CTGGTATGAC CCACTCTAGC TGAGCTGTGC AGAGACTGAG 540
ATGGTCACCT CAAAGAGCAG GGGACCCCGT GTCCAGACTC TGGGGCATGC TGGCAACCTG 600
AGGAGTCTGC GGGAGTGGCC TGATCTGTGC TGCTTGAGGC TTTTTGTCCC AGATCACACT 660
GTACTTGCTC TGGTGTGCCA CAGCGCATCC ATCTCTGTCT TCCCTTCTCA GGTCACCTGC 720
AGACTCCCAA GGACAGGGTC ACATCCCATC TGCGTCATCT CTCAAGGTGC CTTTCACGAT 780
CCTCACCCAT AGGCAGTTCA TTCAGTTACT ACTGGCGGAC TGTTGACATT GACCATCTGC 840
TCTACGTTTT TGTCTTTGGA GACTTGAGTC TCTTTCCATT CTCAACCTCC ACCCGCCACC 900
TCTTTTTTCC CTCTGCTCTG TTAATACACC CTACCAGAGC TGCTCAAATT CCACATGGAG 960
CAGAAGCTCC ATGATAAAGC CCCTTCCCTG CTCTGCTGCA AATAACCTAT TAGGGAACAC 1020
AGTTAAGGAG TTCCCAACCC TTTTAATTTT GGGACAATGG ACAGTGCCAT AGAGGGACCT 1080
GTGGAAATCA ACCCCTTCAC TGCTGTGGTG GGTCTGTGGA GTCCATTTCA GAACACAGGC 1140
CTTCGAAGAC CTGGGAGGGG GCCCTGCAGT AAGGCCCCAT AGGGATTCCT CTTTCTCATT 1200
TGGTTGAGAC CATCACAAAG GGACCAATGA CTTTTTTTTT TTTTTTTTTT TTTTGAGATG 1260
GAGTCTCGCT CTGTCATCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC AATGCAACCT 1320
CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG GGATTACAGG 1380
CGCACGGATA ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA 1440
TTATGTTGCC CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT 1500
GAGCAGGGTA TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT 1560
TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA 1620
GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT 1680
GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA 1740
GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT 1800
GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT 1860
GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT 1920
TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG 1980
AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA 2040
ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC 2100
AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC 2160
CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG 2220
CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC 2280
TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC 2340
TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC 2400
ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA 2460
AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA 2520
ACAATCATTA AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT 2580
CTGAAATCAC CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG 2640
ATCTGTGACG ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT 2700
GGGGCTGGTG TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA 2760
TCCCTACCCC AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT 2820
CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG 2880
TTACAAAGGC CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG GAAGTATGAT 2940
TCAGGAGAAA GAGAGACCAG GACAAAACTG TGATTACCTT TCTCCATGTG GGAATCAAAA 3000
TGCCAGGGAT CTGGTACATT AAGAGAGCAG AGGATGGAGA GATGGCTATA GACTGGAGAA 3060
ATTGCATTGG GAAACTACAT AGAGAAGGTG GAACTAGGGC TAATAGTGTT CTAGGCAGGA 3120
GACTCTGCAC AAACAACAGC ATAGAGCAAA CTACTGCACA TGGCCAGGTT CCATAAATAA 3180
AGTTTGTTTT 3190