EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-20832 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr19:3397020-3398480 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr19:3397822-3397833CCACACCCTCC+6.32
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00151chr19:3396545-3400822Adipose_Nuclei
SE_00856chr19:3396896-3399843Adrenal_Gland
SE_01707chr19:3396862-3399499Aorta
SE_02932chr19:3397508-3399335Bladder
SE_03322chr19:3396885-3399383Brain_Angular_Gyrus
SE_04083chr19:3396809-3399508Brain_Anterior_Caudate
SE_05012chr19:3396747-3399708Brain_Cingulate_Gyrus
SE_05799chr19:3396317-3399866Brain_Hippocampus_Middle
SE_06831chr19:3396600-3399704Brain_Hippocampus_Middle_150
SE_07968chr19:3396490-3399689Brain_Inferior_Temporal_Lobe
SE_08810chr19:3397134-3397372Brain_Mid_Frontal_Lobe
SE_08810chr19:3397750-3398759Brain_Mid_Frontal_Lobe
SE_26149chr19:3396944-3399508Duodenum_Smooth_Muscle
SE_26532chr19:3396865-3401918Esophagus
SE_29960chr19:3398027-3399405Fetal_Muscle
SE_31377chr19:3396888-3399837Gastric
SE_34490chr19:3396139-3399302HCT-116
SE_40606chr19:3396838-3401997Left_Ventricle
SE_42110chr19:3396838-3399637Lung
SE_44438chr19:3396909-3399507NHDF-Ad
SE_44948chr19:3396892-3397903NHLF
SE_44948chr19:3398152-3398839NHLF
SE_46637chr19:3396929-3399336Ovary
SE_47452chr19:3396754-3397994Panc1
SE_47457chr19:3396960-3399379Pancreas
SE_48051chr19:3396445-3405757Psoas_Muscle
SE_48561chr19:3396901-3399662Right_Atrium
SE_49442chr19:3397242-3398008Right_Ventricle
SE_50148chr19:3396852-3399528Sigmoid_Colon
SE_51098chr19:3396080-3401850Skeletal_Muscle
SE_52975chr19:3396869-3399323Small_Intestine
SE_53320chr19:3396887-3399777Spleen
SE_54509chr19:3396483-3399710Stomach_Smooth_Muscle
SE_65251chr19:3396175-3399700Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1933973403398017
Number: 1             
IDChromosomeStartEnd
GH19I003396chr1933967083399668
Enhancer Sequence
TGTGTCTGCA TGCGTGTCTG GGGTGCATTG TGGGGGGATT GCAGGCGTAT TGAGGGCTTA 60
CCAAGTGCCT GGCTCATCTG AGCCCTCAGG AAACCACATT GTTGGCAGCT ACCTCACCGT 120
CTCACAACCA CCCGCTGAGG TTGGAATGAT CATTAACAGC ATTTAACAGA TGGGGAAACT 180
GAGGCCTAGA GAGGCAAAGT CACTGGCCTA AGGTCACATA GCTAAGGAGC ACAGTCAGGA 240
TTTAAATCCA AGCCTGGGAG ATCCCAGGAC CCACAGTGGG CACCACATAA AGGGGCTGTT 300
TGGGGTATGG CAGGGACTGC CCTGGAACGT TCCGGATCCT GCCTTTGGGC CTACAGGGCT 360
TTGGTGCCGG TGAGCAGGCC GCAGGTTCAG CTGGCTCAAG GAGCAGCTTC AGGGCTGCAG 420
CCAGGCTGGG GGCTGGGCAG GTCTCAAACC CCTGGACCTG GGGAATCAGG GAGGTGTGAG 480
CTGCATCTGA GGTCGGGTGT CTCTGTGACT CTGTCTCTGT CTCTCTACCT CTGATTCTCC 540
CCAGGCTGCC TTGTCTCAGT CCCTGTCTAT TCCCACCCCA CCTCGCTCTC TCTCCCGGCC 600
TTGCGAGTCT CCTCCCAGCC CCCCATCCCA CCCAGTGGGC TGCCCGGAGG TGGCGGCAAC 660
GGGGCAGCTG AATGGGCCTC TTGTTCCTGG CCACACCCGC CCCTTGGGGT CACCCTGGGA 720
CATGCCCAGG CAGCGTGGCT ACCTTAAAGG GCCAGTGCTC AGAAAGAATG TGAGCGGGGG 780
AGGCTGCGTC CACTCCCAAA TCCCACACCC TCCCCAAGGT GGACCACTCA TGTGTCTGAC 840
GGGGGTGGGG AGCTGTGTAC CTACACACCC TCGTGGCTTG GGGGAGGCCT GTCTGGAGCA 900
GGAGATGTGA TAGGGTTTGG GTTTGACCTT GGATAAATCC CTTCATCTCT CTGTGCCTCA 960
GTTTCCCCAT CTAGATCAGG GGGCTCCTTG GTGCCACCCC TGTGGGTTGC TGGGCAGATG 1020
GCATATTATC CAGGATTTTG CACACAGTTG ACACTCTTCC GGCGCCCACT GTGCATTGAT 1080
AGAGCACCTG CTGTTTCAGC CCAGCATTCA TCCGCCGTGC AGACTTGGCA ATTCCTTCTT 1140
CACCTTGCTC CGTGCCTCAG TTTCCCCAAA TGCAGAATGA GGCGATGGCT GTCTTAGCTT 1200
CACAGAGAGC TACGCAAGGA TTGAGTCGGT TCGTGGAATT AGAGGGTATT AGGGAGAAGG 1260
GCCTGAAACA CTGCCAAGTG TCACCTCCAC TGGCGCACTT ATTGAGCGCC AGCTGCATAC 1320
CAGGCCTTGC TGAGGAAGCC TCACTGCAGA GGTTGCAGTG AGCTGAGAGG CAAAGGCCAC 1380
CCAGCCTGGA TCTCACTCTG GTGTCATCGC CTCCTCCCTC TGCTCAGGGT TGTGCAGCTT 1440
CAGGCTGCTC CCCTGCCCTC 1460