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

TagContent
EnhancerAtlas ID
HS048-00780 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:27889840-27892660 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:27890271-27890282GCTTCCCGCCC-6.02
HNF4GMA0484.1chr1:27890632-27890647GGAGGCCAAAGTCCA+7.22
Hnf4aMA0114.3chr1:27890633-27890649GAGGCCAAAGTCCAGG+6.26
RREB1MA0073.1chr1:27891686-27891706CCCCCACCCACCCGCCGAGG+6.28
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00527chr1:27889462-27891915Adipose_Nuclei
SE_00861chr1:27886075-27904718Adrenal_Gland
SE_01588chr1:27886149-27904879Aorta
SE_02913chr1:27890049-27890615Bladder
SE_02913chr1:27891079-27891732Bladder
SE_03261chr1:27889156-27892628Brain_Angular_Gyrus
SE_03939chr1:27886198-27895237Brain_Anterior_Caudate
SE_05478chr1:27885928-27895152Brain_Cingulate_Gyrus
SE_05814chr1:27880294-27902223Brain_Hippocampus_Middle
SE_06945chr1:27886514-27895216Brain_Hippocampus_Middle_150
SE_07770chr1:27885748-27895172Brain_Inferior_Temporal_Lobe
SE_08953chr1:27890875-27891588Brain_Mid_Frontal_Lobe
SE_14757chr1:27885672-27892439CD4_Memory_Primary_7pool
SE_23479chr1:27888886-27895065Colon_Crypt_1
SE_24168chr1:27889383-27892160Colon_Crypt_2
SE_24711chr1:27889725-27892508Colon_Crypt_3
SE_25901chr1:27889480-27892932Duodenum_Smooth_Muscle
SE_26518chr1:27885702-27904919Esophagus
SE_27625chr1:27889852-27891463Fetal_Intestine
SE_28547chr1:27889632-27891469Fetal_Intestine_Large
SE_29557chr1:27886726-27904956Fetal_Muscle
SE_31394chr1:27886081-27904513Gastric
SE_33503chr1:27886818-27904912H2171
SE_34367chr1:27889551-27891748HCT-116
SE_34755chr1:27889435-27891507HeLa
SE_36974chr1:27887536-27905229HSMMtube
SE_39896chr1:27887871-27891386K562
SE_40593chr1:27885841-27904966Left_Ventricle
SE_42106chr1:27886079-27904957Lung
SE_46630chr1:27886679-27892191Ovary
SE_47670chr1:27888826-27892075Pancreas
SE_48058chr1:27885887-27904727Psoas_Muscle
SE_48567chr1:27886102-27904727Right_Atrium
SE_49444chr1:27886820-27892209Right_Ventricle
SE_50130chr1:27886169-27892585Sigmoid_Colon
SE_51091chr1:27886184-27904991Skeletal_Muscle
SE_52467chr1:27889204-27891715Small_Intestine
SE_53892chr1:27886040-27904947Spleen
SE_54527chr1:27885939-27904929Stomach_Smooth_Muscle
SE_65253chr1:27886204-27900313Pancreatic_islets
SE_68682chr1:27886365-27891995H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12788986027891017
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
ACACAGCTGA CCAAGACACA CACACACACA CACACACACG TGGGACAAGT CCCATCTTCC 60
AGGTGTGAGG AAGGCATGGA CCCCTCCACC CACCACACAG CATGAGGCAG GGACATAACC 120
TCGCCCCTGC CTGGGAATCC TCCCTGCAGA CTGTGGGATG GGTACACAAC ATGTCACCTC 180
CCCGGCTGCC TTGGACAGGT GACAGCCCAC CTCACCCCTC CCCCATCACT GTCACCAGCC 240
TGGGTGGTGC CGTCCCTCTG CCTGCAGAGG CGTCACAGCT CACACGGCAT GAATGTCACC 300
CCAGCACTGC CAGAGCCGGG CACAGCCACA CATTGCCCCA GTGACAAACA CCACTGGCCC 360
CAGAGGAGGT GAAGGCACAC AGGGCTCTGG TGTGACCTTG GCCTCTGGAC ACCAGGAGGG 420
GAGGTGCTGT GGCTTCCCGC CCAGTGGCGG GTGCTGGGGG AGAGGAGTGC TGGGGAGGAA 480
GCTGCCTGGA CACACTGACT ACCTGGAAAT GCCACCTCCC CCAGCCCTCA CTCCACTCCA 540
TTTCTTATTC ACTGTAGTTG TGTATCTAGG GAGGGGGCTG AATGAGTGGT GGAGGGAGGG 600
CTGTCCTGAG GCGCTGTTAC TATGAGACTG CTTAGAGATC AGTGGGGAGT AGGGCGGTTA 660
GGGGTTGCTA TCACCATGTG CTCAGTGGGA AGAGTATGGG ATAATGGCTT GAGACCCCCA 720
TAGCTTCCAG GGGAGCCCTT CTTCCTTACA AAGGCCCCCT CTCCAAACTT CAGGCCACAG 780
AGCTGGGGAC AAGGAGGCCA AAGTCCAGGA ACATGACTCA CCCAGGGAAC AGGCCCAGCC 840
TGCTGGCCAT AGTGGTGAGG GAGGCCAAGA GCCAAGAGGC CTGGGTTCCA GTCTGAGCTC 900
CTCCAGGGCC AAGCTGGGTG ACCTTGGAGC AGCAGCTCAG CCTCTTTGGC TTCGGGGAGG 960
GGGGAAGGGG CCGCAGTGAG AGAAGTGCCA GGGTCAGAAA GAAGAAGCTG AAGCTGGAGA 1020
CCAGCAGGCA GAACTTCAGG CCACAGAGGG CTCCAGCCCG CCTCCCCTGC TCCCCTGCTT 1080
CCTCACAAGG AACCTCATCT TCCTCATCTG TACAAAAGGG ACAAGAGTGC CAGCCTCATG 1140
AGACAAGGTA GCATAAAGTG GGCCGCTCCT CAAGAAATGG GAAGCTTCTG ATTGAAGAGA 1200
GGGAGAAATA GACTAAGAGA CTTGCCCAAG CCACAGAGCA AATTAGGATC AGCTGAACTC 1260
AGCCTCCATC TCCTGGCTCC CCACCTGGAG CTGTTTCTTT AAGACTGCTT GGAGGTCAAG 1320
TGTGGAGGGG GACAGGGGAG ATGTTGGGGT GTTGTTGGAT GCAGTGCCTC CCTGCCGCCC 1380
GATGAAGACC AATGAATCTG ATAGGAGTCC ACCATGCCCT ACCTTTACCC TAAACCCCAC 1440
TTGGCCCAAA GCTTGGACAA GAGGAGTGGC TCTAAGGGGA GGGAGGCACC CCACCTCCCA 1500
CCCCATCATG ACCAGCAGCA GCACCTGGTG CTTGGAAGGA CTAGAGGACC TGAGATGTCA 1560
GTGTCTAGGG CCCCTCGTTT TACAGGAGCC CAGAGAGGGA AAGGCCTAGC CTGAGGTCAC 1620
ACAGCACGAC AGCACAAGAG CCTAGAGTCC TGGCCACGGA CAGCCTCAGA GCAGAGTCCC 1680
CCTAGCCCCT GGGGGTGGCT GGAGCTGGGG GGCCCTGGGG GACTGAGTAA AGCGTGGCGA 1740
CAGATGGCCT GCCGAGGCAG CGGCGATCTG GGCGGCTGGC AGGCATGCTC GCTCCCGCGC 1800
AGGGAAGCGG CTAATTTTAG CTGAGGCCTC GATGCCAGCT TTGTTCCCCC CACCCACCCG 1860
CCGAGGGGGC CCAGCATGCC TTGCGTGCAA CCTGCCTCCC CCAGGCACCC CTACTCCCCC 1920
GCCTGGCCCC TTGGTGAGTA GTGCCCAGAC CCCAGGATCC TAGAACGGTC TGCCTGACCA 1980
GGCCTCACCA CACCCAGAGG TGAGGCCTGA CTCCCCTACC CCAGGGCCTG TTTGCCCACG 2040
ACTCCAAGCT CATTCCATGA AGAGGGGCGA GAGAGGAAGG ACAGAGGCCA CTGCCCAGAC 2100
TGGGAGGGCG GGCCAGACAG CAGGGGCTGC CAGTCTTGAA GGGAGGCGAG GCACTGTCCT 2160
CCACCCAACC CTTAAGGAGA CAGGACCCTG ATTCCACCCA TGCCCTGGAC AAACATTCTG 2220
TCTGGTGTCC CCCGGCGCTG GTGAGCAAGG GGCGGGAGTC ACTCTAGTCT TTCCTTGTTC 2280
CTCATAACTT TGAGTTTGTT CCAGGAACTC AAAGCACTTT AAAGAAGTCA GACATGAAGC 2340
AAGGATAGTA TCCCTATACC ATCTGGGGAA ACTGAGGCAC AGTCTGAACT TGCCATCATT 2400
TTAGCAAGGG AAGGGACAAA TCCCAAGAAT CAGTGAGGCC TGTTCTCTAG AGAGCTTCTT 2460
GGGCCAGTTT AGCTCCTGGA ACTATCTTCT GTTCCTACCC TGGGCTAGTG GAAGGTAGAC 2520
TAGATGGATG GAGCCCATCC CCTAAAACCC TGGAAAGGCA GACTCACACT CTTGTTTCCT 2580
GGTGCCACAC TCTCTGTAGG CTCTTCAACC TTGCACCCTC CATTTCAGGT TCAACCACAT 2640
AAGCCCAGTG GGGCTTCCAG GACATCTGGC CCCTACTAAA AAGAGGGATC CTTTGGGGTG 2700
ACTCTGGAGC CCTGCCCCCT GCACCAGCTC CCCAATCTTC ATAGGCCTGG GAAGGAAACA 2760
ACCTGGTAGG AAATAGAGTA AGGAGAACTG AAAGGCCCAG CTCTGAAAGA AAGATATGTA 2820