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

TagContent
EnhancerAtlas ID
HS197-20509 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr8:28225590-28227950 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr8:28227572-28227584AAAAAAACATTC-6.52
IRF1MA0050.2chr8:28226349-28226370CTTTTCTTTCTCTTTTTTTTT+7.09
MAFGMA0659.1chr8:28225659-28225680TGATTGCTGACTTGGCATTTT+6.05
NFAT5MA0606.1chr8:28227666-28227676ATTTTCCATT+6.02
NFATC1MA0624.1chr8:28227666-28227676ATTTTCCATT+6.02
NFATC3MA0625.1chr8:28227666-28227676ATTTTCCATT+6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00229chr8:28220519-28226745Adipose_Nuclei
SE_00229chr8:28227525-28228529Adipose_Nuclei
SE_01444chr8:28224917-28225955Adrenal_Gland
SE_01444chr8:28226792-28227351Adrenal_Gland
SE_09976chr8:28222576-28225906CD14
SE_09976chr8:28227441-28229948CD14
SE_10881chr8:28219708-28248222CD20
SE_14002chr8:28226882-28229434CD34_Primary_RO01536
SE_17678chr8:28224218-28226054CD4p_CD25-_CD45RAp_Naive
SE_17678chr8:28227433-28228879CD4p_CD25-_CD45RAp_Naive
SE_20270chr8:28222275-28226017CD56
SE_26645chr8:28222210-28226385Esophagus
SE_26645chr8:28226648-28227573Esophagus
SE_26645chr8:28227689-28229536Esophagus
SE_27701chr8:28220859-28228312Fetal_Intestine
SE_28577chr8:28220748-28235445Fetal_Intestine_Large
SE_31606chr8:28224896-28226285Gastric
SE_31606chr8:28226832-28227525Gastric
SE_36706chr8:28226411-28227963HMEC
SE_40988chr8:28224652-28226382Left_Ventricle
SE_40988chr8:28226491-28227592Left_Ventricle
SE_42550chr8:28224850-28226348Lung
SE_42550chr8:28226724-28227568Lung
SE_42550chr8:28227670-28228551Lung
SE_47708chr8:28225839-28226213Pancreas
SE_47708chr8:28226906-28227577Pancreas
SE_48797chr8:28224901-28226325Right_Atrium
SE_48797chr8:28227685-28228525Right_Atrium
SE_52497chr8:28224785-28225847Small_Intestine
SE_52497chr8:28226685-28227591Small_Intestine
SE_53710chr8:28224840-28225847Spleen
SE_55734chr8:28219906-28226537u87
SE_55734chr8:28226727-28228705u87
SE_58644chr8:28219872-28277477Ly1
SE_59813chr8:28219869-28277603Ly4
SE_61002chr8:28174118-28277761HBL1
SE_61739chr8:28219999-28279573Toledo
SE_62508chr8:28220381-28270893Tonsil
SE_65386chr8:28224811-28229860Pancreatic_islets
SE_67509chr8:28219906-28226537u87
SE_67509chr8:28226727-28228705u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr82822674328227521
Number: 1             
IDChromosomeStartEnd
GH08I028363chr82822052128234313
Enhancer Sequence
GTGTGGTTAA ACCTGATTTA AACTGTTCTC AAACCACATG ACAGTTCCAG AAGGAGGTGG 60
GGAGATGGAT GATTGCTGAC TTGGCATTTT ACCCAGAGCC AGGACTGGAG GGAGGGAACC 120
AGGAGCCGAG TATCCCTGGG GAGAACAAGC CTCACAGAAC TAGCAATTCT AGCAGTCTTC 180
AGGGTAAACT TCTAAGAGAC CTGCACAGGA CCTCAAAGCA CCCACAAATG CTTGAATGGC 240
ACTCAGGTTT ATACTCTCTT GAATGCACAC GCTGGGGGCT TCTCTTCTTT CCCAACTTCC 300
CAGCAACTCA ATAAAATATG AAGGAACAAC ATTATCCCCA TTTTAGAGCT GAGAACACAG 360
GTTCAAAAAG GTCACCTATT TGTCCAAAAT CCCAAAGCTA GCAAGCAGTG GCATTGTCAG 420
TTTCCCGCGC TGTCCTGGTC CAGTTCTCTC TTCCCCACAA GTGGAGACCC AGCAGCAAGG 480
CGCGGCTCAG GCCTGGGGAG GGTGAGTTGG GGGGATCCAG AGGAAGAGAG TGAGTTTCAT 540
GGAGAAGGGA TTTACTGGAA GCACTTGCAG TAACAACAAG CAAAAGCTGC CAATTAAAAA 600
AAAAAAAAAA AGCTGCCATT CCAAAAATAT AAAACACAGA CGTGAGAGTT TTAAAAGCCT 660
AACAACGCCC CAGGTGCCAA TCCCAAGAGG ACAAAAAGGG TTCCTACATT CTCGCTCCTT 720
GAAGAAAGCA GAGGAACACA GGAACATGGA CTCTACTTTC TTTTCTTTCT CTTTTTTTTT 780
GAGATAGAGT CTCGCTCTGT CGACCAGGTT GGGGTGCAGT GGCGCCATCT CGGCTCACTG 840
CAGCCTCCTC TTCCCAGGTC CAAGCAATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAT 900
TACAGGTGCC TGCCACCATG CCGGGCTAAT TTTTGCCTTT TTGGTAGAGA TGGGGTTTCA 960
CCAAGTTGGC CAGGCTGGTC TCGAACTCCT GGCTTCAAGT GATCTGCCCA CCTCGGCCTC 1020
CCAAAGTGCT GGGATTACAG GCATGAGCCA CTGTGCCTGG CCAATTTTTT TTTTTTTTTT 1080
TTTCATTTAG GAAGTTAAAG TAGAAACACT ATTTGGAACT CAAAAGTCAT TTGAATGGAT 1140
CATCACATTC CCTGACAATG CCAAACAAAG GAGAATCACT CCTGAGGGTG AAATGGTTAA 1200
AGGAGAAAAC TGGTTTGGAA CTCAAATGTC ACTTCAATGA ATGATCACAT TATCTGACAA 1260
TGCCAAACCG ACAGGCAGGG GAGCCTGGCA GGAGGATGAG AGCTACCTGG TGACTCACCT 1320
GGCTGGAATT AACATGTCAT AAAAAGGCAA CTGCCCTCTC CTTGCGGTGG GTAATCAAGG 1380
CACCCATTTA GAGGCTTGCT GGTCAAAATG AACCAACTCC AGTGTTCCAT GCTTGGAGCT 1440
CAACACTAAG TCAGACTGCT CTGGCCCTGG AGCCAAAGCC AGTGACCGAC CCCTGCCCAT 1500
TACCCATGTG ACTAGGTGCC TGCCCCGCTC ACTTTCGGTA CCGGGTCTCT TTCCTGCTCT 1560
GTTCCCCCAA GCCTGAATCT CAGCCTTGGG GCCCTGCCCT CAAGCCTCCC CCAGGTGGGG 1620
CCTGGCCAGC CTCTGGGAGC TAATCCCGCC CACACGGGTG GGGGCAGACC CACCTGGGGA 1680
GGGACTCACC GGAACCCCCG GGAAAGGGCC CCAGAGCAGA AAAAGCCCAG CGTCTTTAAA 1740
CATATCAGCC CTGCTGCTAT GCAACATGTG GGTCCAGCTC TTGACCATGC ACCAAACCAA 1800
ATATTAAGAA GCCTAAGAGT CAGACCCTGC CCTTAATGAA TTTGGGGCCT AAATGAGCTA 1860
CCACCTGGTC CACACAGCCA GCACTTGTGT ATAAAAGCAC TTAATACGCT CTGAAGCTAC 1920
ATTTATGTAC TGTGTTGTAT AATGAGATGA ATGAATGAAC ATTTGCATCT CTCAGGAAAA 1980
TGAAAAAAAC ATTCAGCAAT CTGACACTGA AGCCTGATTT TTAAAAAGGG GGTTTTTAGA 2040
ATGGAGCCCA TGAGTTAGAT GAATATCCAT GTGAACATTT TCCATTTTTG ACATCAGTTA 2100
GATAAGTCAA AATAAAATAT GTTATGAATC TAAAAAAAAA AAATCCACTG AGTGACTGGA 2160
GGTTGAAGGA GACACAGGTT TCACCCCAAA AACAGAAAGT CAGCCTTAGT GACGAGAAGA 2220
CAGGCACCAT CGGGGAAGAT TTAAATACAT AGTGGAAAAT AAACGGAGTG GAGGAGGGGC 2280
TCGCCCAGGG CTCAAACCAC TAAGGAAGTG CCTTAAACGT ATTTTTCTCT GGAGGAAGCC 2340
ATTTAAGGAA TCTTTATGCC 2360