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

TagContent
EnhancerAtlas ID
HS095-00629 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr1:27843740-27845320 
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: 30             
IDCoordinateTissue/cell
SE_02913chr1:27844536-27845036Bladder
SE_05196chr1:27845131-27856743Brain_Cingulate_Gyrus
SE_05814chr1:27844227-27851238Brain_Hippocampus_Middle
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
TCCAGCCTGG GCAACAGAGC AAGACTCTGT TTCAAAAAAT AAATAAATAA AAATGAATTG 60
TAATGGGGCA TAGAAGAGAA ACTCATTTTT GTTGGGGAGG TGGGGGTCCA GAGAGGCTTC 120
TTAGAGAAAA GGAACATCTG TGTTGGGCTC TGAAGGATGA AGAGTTCACC CGGAAAAGTG 180
GCAGAGGGCA TTCCAGGAGG AATGTATTTT GTGGACAAAG GCCCAGGGAT ATGGAAGGAT 240
ATGACCTGTT TGGGTGTGGC TGAACACAGA GTTGGCTGAG AGGAGTGGTA GGAAATGAGG 300
TTCGAAAGGC AGTTTTGAGG GCCTCCAGTG CCTTGCTATT GAGGGCAGAC TTTAAAGGAC 360
TGGGGAAACA GAGCAGGAGT TTAAGGGCTG GGAAGGGACA GGATTATACC TATTTTATTT 420
TTATTATTTA TTTATTTAGA GATGGAGTCT TGCCCTGTTG CCCAGGCTGG AGTGCAGTGG 480
TGCAGTCTGC TCACTGCAAC CTCCTCCTCC CAGCTTCAAG CGATTCTCCT GCCTCAGCCT 540
CCCAAGTAGC TGGGATTATA GGCATGCACT ACCACGCCCA CCTAATTTTT TTGTATCTTT 600
AGTAGAGACG GGGTTTTGCC GTGTGGGGCA GGCTGGGTCT CGATCTCCTG ACCTCGTGAT 660
CTACCCTCCA CGGCCTCTCA AAGTGTTGGG ATTACAGGCG TGAGCCACGG TGCCTGGCCT 720
TATTGCGCCT ATTTTAGAAA GGTGATTCTA GCCGCAGTGT GGAGCGTGAG CTGTACGAGG 780
AGAGCCTGGC TGTCGGGGAG CAGATCTGAG CACGCTCCTC ACCAGCCCTA GCTCAGGCTC 840
GGACCTCTCT GACTTCCTGC CTTCCCACGT GCTCTTGCCT CTGCTTAGAG TATCTTTCCC 900
TTGACTTTGC CTGGCTAACT CCTTGCCCAC CTTCAGGTCT CAGTTTAGCC AGCACTTCCA 960
CCCGGAAGCT CTACTAGACA CCCCTCCCAG TCCAGATTAG ATGCTCCTAC TTACTCCTCC 1020
TCTGTGCTTG CAGACCTGCC CACCTGCCTG CCTCGTCGAC TGGACTCTGG CCAAGGGCAG 1080
GGACTGTGTG GCACTGCTCA CTGCTGTATC CACAAGGCCC TAAGGCATAA TGCCTGGAGC 1140
CTCAATCCAT GATCGGTAGG GAACGAATGA ATGGCTAAGC CTGTTGGGGC AGGTGTGATA 1200
GTTTGAGTGA AAGTGACAGG GTCTGCGGTG GCAGCGAGGA GAGAAGAGAC ACGATAGAAT 1260
TGACGGGACC CAGGAATCAT GAGAGGAGAA CACAGGGAGA GAAGAAGGAG TTGGTGATGA 1320
CTCAGAGGTG TTTTTTTTTT CACCTGGGTA AGCCCTGTGC CTCTAACCAA GATAGGAGCC 1380
ATGGAGGAGG GGGTTGGAGG GAGGGAGGGA GGAGTAGGCC AGGGCAGAGG GGCAGGGCGG 1440
AGCCTTACCT TGGTAGGAGA CTGGGGCCCT GGCCCAGGCC GTTCCTTGGA GTATTCTTCC 1500
CTTCTGGGAT GCTGTGCACA CTGATGGATC CTCAGCAATG TCTGTGACTG TCCAAATGCT 1560
GCCACCTTGA CCACTCTAAC 1580