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

TagContent
EnhancerAtlas ID
HS182-01812 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr1:206754810-206756600 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:206754991-206755009GGAAGGAAGGAAGGAAAG+10.53
EWSR1-FLI1MA0149.1chr1:206754999-206755017GGAAGGAAAGAAAGAAAG+6.95
EWSR1-FLI1MA0149.1chr1:206755177-206755195TGAAGGGAGGAAGGTAGG+7.01
EWSR1-FLI1MA0149.1chr1:206754987-206755005AAAAGGAAGGAAGGAAGG+7.95
EWSR1-FLI1MA0149.1chr1:206754995-206755013GGAAGGAAGGAAAGAAAG+8.46
NFICMA0161.2chr1:206755867-206755878TACTTGGCACA+6.32
ZNF263MA0528.1chr1:206754996-206755017GAAGGAAGGAAAGAAAGAAAG+6.02
ZNF263MA0528.1chr1:206754992-206755013GAAGGAAGGAAGGAAAGAAAG+6.03
ZNF263MA0528.1chr1:206754964-206754985GGGGGAGAGAGAGAGAGAGAA+6.38
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_09327chr1:206745188-206758382CD14
SE_10603chr1:206747310-206756416CD19_Primary
SE_11004chr1:206727079-206757887CD20
SE_11917chr1:206750311-206757762CD3
SE_14503chr1:206746009-206758997CD4_Memory_Primary_7pool
SE_16490chr1:206750757-206757114CD4_Naive_Primary_8pool
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_27304chr1:206755912-206765002Esophagus
SE_31229chr1:206755155-206757244Fetal_Thymus
SE_53261chr1:206746644-206756568Small_Intestine
SE_53552chr1:206746429-206757806Spleen
SE_59167chr1:206727342-206757447Ly3
SE_62534chr1:206724532-206763666Tonsil
SE_65624chr1:206752745-206755870Pancreatic_islets
SE_65624chr1:206756181-206757996Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1206754982206755508
chr1206754868206756159
Number: 1             
IDChromosomeStartEnd
GH01I206573chr1206746529206757654
Enhancer Sequence
ATCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATTGCTTG AACCTGGGAG GCAGAGATTG 60
CAGTCAGCCA AGATCGTGCC ACCGCATTCC AGCCTGGGTG ACAGAGGGAG ACGAAAGAAA 120
AGAAAGAAAG AAAGAGAGAG AGACAGAGAG AGAGGGGGGA GAGAGAGAGA GAGAAAGAAA 180
AGGAAGGAAG GAAGGAAAGA AAGAAAGGAG GATGTCAGCT GTGCTGAGGG GTTGGAGGTG 240
GGAGGCTGGA GCCACGCCAG CTCCTCTTGG CAGCCAGAGC CTGACATTGC ATCGGTTCTG 300
TGGGATTGGA AAGTGGAAGG AAGTGATGGC AGGTTGTTCA GGGTGGCGTG TCTCCCACAT 360
GGCTTGCTGA AGGGAGGAAG GTAGGGCAAA GCTCTGTCAC GGAGGGGGGG CCCTGTTGTG 420
TTCCGCGGGG TGGTGGTGTG ACGTCGCGGC AGCTGTGAAA TTCCCCAGCC AAACCCAGAC 480
ACCCACAGGA CAGTGTCAGA TGGTGTCAGA GTCATCCCTC ACTGGGCCTC AGTTTCCTCA 540
TTTACCAAAG GAGAATCCTG ATCCACCCCA AGTCTGCTAC ACTTGAACGT CAGGCAAATT 600
CTGGGTGGGT TCTGACCAAC CAGTTCCCAC ACTCCCAGCC ACTCAGGGAC AGTGTGAAGA 660
TAAAACCGGG AGGTGGGTAA CAGTGAACTT GAGAGAGAGC CAGAGAACTG ACTGAGGGAC 720
AGTGGCTTCG ACCCCAGAAT TCACCCCTGT ATTGTCTCTA CAAGGTGAGG GCCATTGACC 780
TCAATCTCCT CAATTTCATT GTTCACTTAT CCTTCCCAGG GGGTGGGAGG AGGAGGGCAT 840
CTGGGAACAT ATGAGAAGAA TGAACACATG GTCTCACAGG AGGAACACAA TGGGACAGAC 900
CTGGAATTTC TGTTTCATTC TGTACATACT GACTGTAGGG TGTGAGGCAG GTTGCTAAAC 960
TTCTCTTAGT CTCAATAGTC TCACCTGTAA GATGGGGTAA TAAACTATCT TACAGACTTC 1020
TGGTTTGTGA GAATCATATG AGATAATGTA TGCCAAATAC TTGGCACAGA AGAAGTGCTA 1080
AGTAAATTCT AGGTGTCCCT GTGCCCAGTA GCGGTTTATC TCCTCTTTTA TGGTAGAGGG 1140
GGCTACAGCC CTTCATCCCT GCCAGTTCAC TCGTTCATTT GACAAATAGA TATTTACTTC 1200
TTGCTATGTG AAAAGCACTG TGGCAAGTGA TGTGGGGCCT GGACTGGTCT CTATGTGTCC 1260
TTGGTCCTTG GGATCTAAGA GAATTCTTGT CTTCCCGATC AGTAGTATAT ACTGGCACCA 1320
TGGGTAGACG CCTGTCCCTC CAGCTGTGTT GTTACTTCCT TGAGGAGACA GACCATGGCT 1380
TGTATTTCTT TGCATCTCCC ATAGCATCAA AGAAGCATCT TTTCCATAGC AGCTTTCCAT 1440
AAGCAAATGC GGCTCTGCTC ATTCACCAGA TTCATAGTCA GTGCCTGAGT GCCAGACGCT 1500
TTCACACTAA TCTCAAGACA AGCCTGTGCA GTAGGTATTG TTCCCATTTC ACAGATGAGG 1560
AGACTGAGGC TTAGAGAAAT CTGAGTTACT TCTCCAGGAG GGCTGGCTAG ACACTGGCAC 1620
AGCTGCAATT TGACCTCTCA TTGTCTCACT CCGAGTCCGT GCAGTTAGTT CCACTCTGCA 1680
GGGCTGGATG CTCACTTCTT GGTTAGAGAG GCTTTGGGGA GGGCGTGGTT GTTCCCTTTC 1740
TCACCCTGAG AACTACTACA CATCCACCTC CACTTCTGTG TCTCTTCCAG 1790