EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-09141 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr14:69416800-69418600 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:69417701-69417719CCTGCCTGCCCTCCTTGC-6.41
FOSL2MA0478.1chr14:69417913-69417924GGGTGACTCAG+6.02
JUNBMA0490.1chr14:69417913-69417924GGGTGACTCAG+6.02
ZNF263MA0528.1chr14:69418085-69418106GAGTGAGGAGGGAGAGAAAGA+6.27
ZNF263MA0528.1chr14:69418088-69418109TGAGGAGGGAGAGAAAGAGGA+7.94
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00359chr14:69414459-69420814Adipose_Nuclei
SE_01544chr14:69411920-69417098Aorta
SE_01544chr14:69417251-69420434Aorta
SE_02315chr14:69417362-69420547Astrocytes
SE_04266chr14:69417860-69419498Brain_Anterior_Caudate
SE_09473chr14:69411857-69420150CD14
SE_17458chr14:69417417-69420388CD4p_CD25-_CD45RAp_Naive
SE_24115chr14:69417535-69418879Colon_Crypt_2
SE_25810chr14:69411075-69417124Duodenum_Smooth_Muscle
SE_25810chr14:69417135-69420777Duodenum_Smooth_Muscle
SE_26589chr14:69417470-69420421Esophagus
SE_28065chr14:69417510-69420636Fetal_Intestine
SE_28974chr14:69417614-69420701Fetal_Intestine_Large
SE_31722chr14:69417476-69420402Gastric
SE_36138chr14:69404230-69420474HMEC
SE_37016chr14:69402168-69421041HSMMtube
SE_38329chr14:69415190-69420541HUVEC
SE_38873chr14:69417408-69420422IMR90
SE_42569chr14:69417379-69420396Lung
SE_45678chr14:69402257-69421189Osteoblasts
SE_47006chr14:69417563-69420364Ovary
SE_47970chr14:69417580-69417977Pancreas
SE_48719chr14:69417459-69420433Right_Atrium
SE_50146chr14:69417457-69420435Sigmoid_Colon
SE_52189chr14:69417379-69418877Skeletal_Muscle_Myoblast
SE_52675chr14:69417467-69420545Small_Intestine
SE_53596chr14:69417436-69420443Spleen
SE_54485chr14:69401836-69420919Stomach_Smooth_Muscle
SE_57035chr14:69417503-69418707VACO_400
SE_64004chr14:69417435-69418987HSMM
SE_65495chr14:69417210-69419260Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146941688669417366
Number: 1             
IDChromosomeStartEnd
GH14I068931chr146939771969420516
Enhancer Sequence
AGGAGTTCGA GACCAGCCTA GCCAACATAA TGAAACCCCG TTTCTACTGA AAATACAAAA 60
ACTAGCCAGG CATAGTGGCA GGTGCCTGTA ATCCCAGCTA CTGGGGAGGC TGAGGCAGAA 120
GAATCACTTG AACCCGAGAG GAGGAGGTTG CAGTAAGCTG AGATTGTGCC ACTGTACTCC 180
CAGTCTGGGT GACAGAGTGA GTTGTTGTCT CAAAAAAAAA AAAAAAAAAA AAAAAAAGAG 240
TTCAGGAGAT GGATGCTGGT GATGGTTACG CAACAACATA CATGTACTTA ATGCTGCTGA 300
ACTGTACGTA CACTTCAAAA TGGCTAAAAT GGTAAATATC ATATTATGTA TCTTTTACCA 360
TAATATATAT GCGTGTGTGT ATATATATAT ATATAAATCA AACATATAAA ATCTGTGGTA 420
TAGAAAAATA ACAGTGTTAC CTGTGGGGAG TTGTTTTTTA TTTTACCACA AGCATGTCAA 480
ACTTTTTTTT TTTTTTGAGA CGGAGTCTCA CTCTGTCGCC CAGTCTGGAA TGCAGTGGTA 540
TGATCTCGGC TCACTGCAAG CTCCGCCTCC CTGGTTCACA CCATTCTCCT GCCTCAGCCT 600
CCCAAGTAGC TGGGACTACA AGCACCCGCC ACCACGCCTG GCTAATTTTT TGTATTTTTA 660
GTAGAGACAT GGTTTCACTG TGTTAGCCAG GATGGTCTGG ATCTACTGAC CTTGTGATCT 720
GGCTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCACG TCCGGCCCTA 780
AGCATGTCAA ACTTTTATCA TAAAACAAAA CAGATATTGA AGACTTGTAA ATCAAAAACA 840
TTTCAAATTG TGATTCAGGA GGGTGTTTAA GACCTCCAGT TAGAGGGGGG CAATGTTATC 900
ACCTGCCTGC CCTCCTTGCC ACCAGCACCA GCCTGCCTGC AGAAGGCCAA GAAACTCTCC 960
CAAGAAGCGA CGAAGGCAGA CGAACGGCAG GGCAGCTGGA TAGCACAGGC CTTCCCTGGC 1020
CCCCCGCCCT TTGAGAAACA GTGGCAGGGA AGCGCCACCC ATGGCCAGAG GCAACGGGGT 1080
GACGGGCAGG CTCCTCCCTG GGCCCTGACT CCAGGGTGAC TCAGGCGCTG GTTTCCCCGG 1140
AAGGAAGTGA GCCAGCCGAC TCTCTTTTTC CCTTTCTAGG AAGACACAAG GGAATGACTT 1200
GGCCCAATCC CAGGGGCCCA GCCTTTTTAC TCAGACTGTT ATGGAGAAAC CACCCCACCG 1260
TCCTCCACTA CAGGAGAGGA AGCCAGAGTG AGGAGGGAGA GAAAGAGGAA ACAGCTCATC 1320
CCACAGAGGA AGATACAGAA AAGGGGAGGC ACAATGGACA AGACAGGGCC TTCTCTTTCT 1380
AACCTCAACT CCCAACATAA ATGCCCAAGG AGGGATGCAT GGAAGCTCTG CAACCCCACA 1440
GACTTGGGCT CTGGTCCTGA CGTTCCCGCT GACTAGCTGT GTGCCCTTGA CTCCGTTTCC 1500
CCAACTCTAA CGTGAAGGTG ATGCAACATT TGATATCCAA GGCCCCTTTC AGCTCTGAAA 1560
CTCCAGGCTC CTGTAAAAGC CGGGTGATGG GCTGGGACTG AGGAAGGCCT GGAGAAGACT 1620
GGACGTGGTC TTGGAACAGG GAGAGCTTTG GGTGTGGAGA CTCGTGCCTG GTACCCCTCC 1680
CAGAAGTAAT GGCTCTAAGT GCAGCACCAG TGTCCCCACC CTCAGGCCAA GTAACCCCAT 1740
CATTCATTCA CTCATTCATT CGTTCGTTCA TTCATTCAAG ATTTTCTAAA CTCTTACCCT 1800