EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS049-00732 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr1:207998920-208000640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2724373chr1207999200hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr1:207999927-207999938ATGTTTACTTA-6.02
Foxa2MA0047.2chr1:207999928-207999940TGTTTACTTAGC+6.52
HNF4GMA0484.1chr1:208000278-208000293TGAACTTTGACCCGC-6.08
Hnf4aMA0114.3chr1:208000276-208000292GCTGAACTTTGACCCG-6.87
IRF1MA0050.2chr1:207999508-207999529GTTTCCTTTCATTTTCCCTCT+6.71
IRF2MA0051.1chr1:207999507-207999525TGTTTCCTTTCATTTTCC-6.49
NR2C2MA0504.1chr1:208000278-208000293TGAACTTTGACCCGC-6.11
Nr2f6MA0677.1chr1:208000278-208000292TGAACTTTGACCCG-6.22
RxraMA0512.2chr1:208000278-208000292TGAACTTTGACCCG-6.92
SREBF2MA0596.1chr1:207999211-207999221ATCACCCCAT-6.02
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00306chr1:207977138-208002770Adipose_Nuclei
SE_01416chr1:207993530-208001102Adrenal_Gland
SE_01610chr1:207977672-208001114Aorta
SE_02940chr1:207994764-208001210Bladder
SE_03274chr1:207994642-208001056Brain_Angular_Gyrus
SE_03907chr1:207991667-208003388Brain_Anterior_Caudate
SE_06993chr1:207991689-208002991Brain_Hippocampus_Middle_150
SE_08580chr1:207991706-208006704Brain_Inferior_Temporal_Lobe
SE_08815chr1:207998887-207999223Brain_Mid_Frontal_Lobe
SE_08815chr1:207999241-207999534Brain_Mid_Frontal_Lobe
SE_08815chr1:207999651-207999905Brain_Mid_Frontal_Lobe
SE_08815chr1:208000135-208000367Brain_Mid_Frontal_Lobe
SE_08815chr1:208000424-208000624Brain_Mid_Frontal_Lobe
SE_09440chr1:207995744-208003407CD14
SE_10475chr1:207994104-208000942CD19_Primary
SE_11488chr1:207992533-208010277CD20
SE_12401chr1:207995997-208000598CD3
SE_13353chr1:207996071-208001084CD34_Primary_RO01536
SE_14644chr1:207995084-208002663CD4_Memory_Primary_7pool
SE_17929chr1:207994596-208002969CD4p_CD25-_CD45ROp_Memory
SE_18828chr1:207994794-208013240CD4p_CD25-_Il17-_PMAstim_Th
SE_20606chr1:207994659-208001166CD56
SE_21313chr1:207995382-208000901CD8_Memory_7pool
SE_21874chr1:207995258-208000511CD8_Naive_7pool
SE_23628chr1:207998491-208001207Colon_Crypt_1
SE_24155chr1:207998607-208001173Colon_Crypt_2
SE_25829chr1:207992121-208003797Duodenum_Smooth_Muscle
SE_26666chr1:207993695-208001206Esophagus
SE_31608chr1:207984660-208002274Gastric
SE_40741chr1:207976619-208001249Left_Ventricle
SE_41597chr1:207997975-208001110LNCaP
SE_42138chr1:207976803-208001181Lung
SE_45086chr1:207995936-208001117NHLF
SE_46988chr1:207996188-208000776Ovary
SE_48128chr1:207976505-208001203Psoas_Muscle
SE_48593chr1:207982190-208002314Right_Atrium
SE_50299chr1:207993725-208002318Sigmoid_Colon
SE_51185chr1:207976162-208002674Skeletal_Muscle
SE_52485chr1:207994685-208001212Small_Intestine
SE_53314chr1:207993859-208001216Spleen
SE_54764chr1:207991828-208013085Stomach_Smooth_Muscle
SE_59011chr1:207980241-208007571Ly3
SE_60122chr1:207993349-208003620Ly4
SE_61319chr1:207994376-208006461HBL1
SE_62794chr1:207980098-208006634Tonsil
SE_65312chr1:207986337-208001141Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1207999163207999611
Enhancer Sequence
CCAAGGTTGA GCATGCCAAT AAAGAAGTTA CCTACTGGTC TGATGACCAA AGGAACGTGG 60
CCTTGATGGC ACTAAAGCAA GTCCCCCAGA AAGGTCCTCT GGTTACTTAA ATCCCATTTG 120
CCATAGTTTC CTTCTCCATG GAAGAAAAAC ATGCCTAAGT TCATGTCAGG ACATTCCTGA 180
TTTATCCAAG AGCCCAGGAT CAAATAAACA AAGGGCTCTG AGCTCTGCCA GGGAGCCTCC 240
TCCTTCAGGA GGCAGAACTA GAGGGAAGTA GGCTTGGTAC AGAGCTGGCC CATCACCCCA 300
TGAACTTGGT GAGTGACGTG GCTGCTCACT GCCATGGCGA TGGGGATGTT ACGGGTGGGT 360
GGAAGTGAGA GAAGAGGCAA ATAAGTCATG AGAGACGAAG CGAAAGCGAG GCAGGGTCAC 420
AGGAGGAACC TACAAAGCCA CAGAATTTGT ACAGAGGCCG ACTGTAGTCT ATGACCGCAG 480
CAAAACTAAG CTGAGTCCCT GCAAAGATAA GTCCCCATCT CAGGGGTGCG GCATGAACCA 540
ACTATGACTC GCAAAAACCT ATGACAACAC TACGTTCAGC AAGGCTTTGT TTCCTTTCAT 600
TTTCCCTCTA AATCTTTTCC TTCCCATGAC CCCGTTGGTA CGGCTTTGAT GACTGGAAGA 660
ACACTAGGGT TTTCGGTTTT GCTCCGGTTT GAATAAAATG ACACAGACAT ACATGGAGTG 720
GTTTTAAAGA GTGGAGAATT TAATAGGCAA GAAAGAAGGA AGAGGCTTTT CCTGTACAGA 780
GACAGAGGGG GGCTTTAAGC CGAAAGAGGG AACCTTGAGT GCGGTGGAAA ACAGCCAGTT 840
ATATGAGGAG GCTGGAGGAG GCAGGATTAA AACAGTCATT TTAGGTACCT CTGCCCAATT 900
CTAGGTCTTC CTTCTATTAA CCTGATTCTA CAAGGCACCA AGAACAAAAA AACCCGAATG 960
GGATGACCAG GAAGCAGAAA TGAATTCAGT TCCAAAAACA TGGGAGGATG TTTACTTAGC 1020
AAGCACGCTC GAGCCTACAA GGAAGCAGTT TTACAGGGTG CTGCATGCAG TGTTTGATTT 1080
CAGGGGGTAA AGATAACTTC AGAGTGGGGA AAAGGTGCTG GCTCCTTCTA CTCACCCTCA 1140
GAGGCTTGGG GAGGCCAGGC CAGCACAAAC TTGAAAAGGC AAGGCTTCAG CTCAAGCCCA 1200
ACAGGTTGCC GGCTCTCTTT GGCTCCTCGG CAGCTACCGG ACTCAGGAAC TAAACAAACT 1260
CTCCAGACTT CATGAGCATT CCGTGGCCTC CGACTGATCT GGGTCAAAAC TTCGAAATGC 1320
CAAAGACAAA GAATTTTTTT CTTTAAAGGG GAATGAGCTG AACTTTGACC CGCCCTTGTT 1380
CAGGGTGTGG AATGCAAGCA CTGTGTACCG GCCACAAACT CCAGTTCGGC AGGCAACAGC 1440
CAGAAAAGCA GTCTTCATGC CGGCTTCATG CCGGCCTCCC TGTCCTGTTT CCTCTTTAGG 1500
GCCAACTCGA CGGGGTCTAG GTCTTTACCT CGCTCTCCAG ACAGGGAAGC TGTGCAGAGG 1560
ACACATTCCA ATCTCTGTTA TCTAGAGCTA GAGTGGATGT TCTAGATAAA TCTGGCAGCG 1620
ATCTGGTCTC AGGTGGAACT GACAGGCCCA GTCCACAGCA AGATGGCATT TCTGTTCACT 1680
CCCTGGGAGC TGGTGGACAA CAGGCGCTTG GTTACCACCT 1720