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

TagContent
EnhancerAtlas ID
HS051-00509 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr1:27843820-27845520 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27844587-27844605TCTGACTTCCTGCCTTCC-6.01
KLF14MA0740.1chr1:27844309-27844323TACCACGCCCACCT+6.59
Klf1MA0493.1chr1:27843990-27844001TGGGTGTGGCT-6.14
PRDM1MA0508.2chr1:27844946-27844956GTGAAAGTGA-6.02
SP3MA0746.2chr1:27844309-27844322TACCACGCCCACC+6.37
SP8MA0747.1chr1:27844310-27844322ACCACGCCCACC+6.32
ZNF263MA0528.1chr1:27845122-27845143GGAGGAGGGGGTTGGAGGGAG+6.7
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_02913chr1:27844536-27845036Bladder
SE_03939chr1:27845236-27851100Brain_Anterior_Caudate
SE_05196chr1:27845131-27856743Brain_Cingulate_Gyrus
SE_05814chr1:27844227-27851238Brain_Hippocampus_Middle
SE_06945chr1:27845183-27851030Brain_Hippocampus_Middle_150
SE_07770chr1:27844238-27856992Brain_Inferior_Temporal_Lobe
SE_23188chr1:27843698-27847641Colon_Crypt_1
SE_24033chr1:27843764-27844291Colon_Crypt_2
SE_24033chr1:27844307-27845471Colon_Crypt_2
SE_24711chr1:27843869-27847003Colon_Crypt_3
SE_25901chr1:27844261-27845577Duodenum_Smooth_Muscle
SE_26518chr1:27843507-27857767Esophagus
SE_27625chr1:27843691-27857024Fetal_Intestine
SE_28547chr1:27843416-27856986Fetal_Intestine_Large
SE_29557chr1:27845136-27850991Fetal_Muscle
SE_31394chr1:27843780-27847429Gastric
SE_33477chr1:27843634-27857256H2171
SE_34367chr1:27844425-27845418HCT-116
SE_34755chr1:27843588-27845742HeLa
SE_35950chr1:27843632-27846014HMEC
SE_36974chr1:27845141-27851091HSMMtube
SE_39896chr1:27844247-27845283K562
SE_40593chr1:27844098-27856916Left_Ventricle
SE_42106chr1:27844182-27851151Lung
SE_48567chr1:27844222-27851412Right_Atrium
SE_50130chr1:27844122-27851113Sigmoid_Colon
SE_51091chr1:27844267-27845360Skeletal_Muscle
SE_52467chr1:27843721-27848576Small_Intestine
SE_57160chr1:27844222-27845429VACO_400
SE_62718chr1:27801410-27856116Tonsil
SE_65253chr1:27843908-27851025Pancreatic_islets
SE_66890chr1:27843634-27857256H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12784446527845239
chr12784390327844052
Enhancer Sequence
ACTCATTTTT GTTGGGGAGG TGGGGGTCCA GAGAGGCTTC TTAGAGAAAA GGAACATCTG 60
TGTTGGGCTC TGAAGGATGA AGAGTTCACC CGGAAAAGTG GCAGAGGGCA TTCCAGGAGG 120
AATGTATTTT GTGGACAAAG GCCCAGGGAT ATGGAAGGAT ATGACCTGTT TGGGTGTGGC 180
TGAACACAGA GTTGGCTGAG AGGAGTGGTA GGAAATGAGG TTCGAAAGGC AGTTTTGAGG 240
GCCTCCAGTG CCTTGCTATT GAGGGCAGAC TTTAAAGGAC TGGGGAAACA GAGCAGGAGT 300
TTAAGGGCTG GGAAGGGACA GGATTATACC TATTTTATTT TTATTATTTA TTTATTTAGA 360
GATGGAGTCT TGCCCTGTTG CCCAGGCTGG AGTGCAGTGG TGCAGTCTGC TCACTGCAAC 420
CTCCTCCTCC CAGCTTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTATA 480
GGCATGCACT ACCACGCCCA CCTAATTTTT TTGTATCTTT AGTAGAGACG GGGTTTTGCC 540
GTGTGGGGCA GGCTGGGTCT CGATCTCCTG ACCTCGTGAT CTACCCTCCA CGGCCTCTCA 600
AAGTGTTGGG ATTACAGGCG TGAGCCACGG TGCCTGGCCT TATTGCGCCT ATTTTAGAAA 660
GGTGATTCTA GCCGCAGTGT GGAGCGTGAG CTGTACGAGG AGAGCCTGGC TGTCGGGGAG 720
CAGATCTGAG CACGCTCCTC ACCAGCCCTA GCTCAGGCTC GGACCTCTCT GACTTCCTGC 780
CTTCCCACGT GCTCTTGCCT CTGCTTAGAG TATCTTTCCC TTGACTTTGC CTGGCTAACT 840
CCTTGCCCAC CTTCAGGTCT CAGTTTAGCC AGCACTTCCA CCCGGAAGCT CTACTAGACA 900
CCCCTCCCAG TCCAGATTAG ATGCTCCTAC TTACTCCTCC TCTGTGCTTG CAGACCTGCC 960
CACCTGCCTG CCTCGTCGAC TGGACTCTGG CCAAGGGCAG GGACTGTGTG GCACTGCTCA 1020
CTGCTGTATC CACAAGGCCC TAAGGCATAA TGCCTGGAGC CTCAATCCAT GATCGGTAGG 1080
GAACGAATGA ATGGCTAAGC CTGTTGGGGC AGGTGTGATA GTTTGAGTGA AAGTGACAGG 1140
GTCTGCGGTG GCAGCGAGGA GAGAAGAGAC ACGATAGAAT TGACGGGACC CAGGAATCAT 1200
GAGAGGAGAA CACAGGGAGA GAAGAAGGAG TTGGTGATGA CTCAGAGGTG TTTTTTTTTT 1260
CACCTGGGTA AGCCCTGTGC CTCTAACCAA GATAGGAGCC ATGGAGGAGG GGGTTGGAGG 1320
GAGGGAGGGA GGAGTAGGCC AGGGCAGAGG GGCAGGGCGG AGCCTTACCT TGGTAGGAGA 1380
CTGGGGCCCT GGCCCAGGCC GTTCCTTGGA GTATTCTTCC CTTCTGGGAT GCTGTGCACA 1440
CTGATGGATC CTCAGCAATG TCTGTGACTG TCCAAATGCT GCCACCTTGA CCACTCTAAC 1500
TCGGCTGCCT CCCCTACAAA TTATTCTCTA CCAATGCACT CTCTCCACTT CCTCCCAACT 1560
CTCATGATTG TAATCGTGTA TCCGTTGACT TGTATTTTAT TCTCAGTGTG TCTTCCTCAC 1620
TAGATTGGAA GTTCCATGAA GGCAGGGATC TCGCTGGTTT TATTGACCAT GTATACCTGG 1680
CAGGCTCCCT GGCACATAGT 1700