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

TagContent
EnhancerAtlas ID
HS111-02591 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr19:13960930-13962760 
Target genes
Number: 5             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr19:13961365-13961376GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:13961366-13961376GGGGCGGGGC-6.02
PLAG1MA0163.1chr19:13962168-13962182CCCCCGTTAGCCCC-6.26
PLAG1MA0163.1chr19:13962236-13962250CCCCCTAGGCCCTC-6.32
SP3MA0746.2chr19:13961364-13961377GGGGGGCGGGGCC-6.11
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00394chr19:13948737-13963116Adipose_Nuclei
SE_00791chr19:13961433-13962030Adipose_Tissue
SE_00791chr19:13962168-13962426Adipose_Tissue
SE_02576chr19:13959489-13964991Astrocytes
SE_09068chr19:13961590-13962107Brain_Mid_Frontal_Lobe
SE_13342chr19:13948702-13962977CD34_Primary_RO01536
SE_14690chr19:13956464-13962797CD4_Memory_Primary_7pool
SE_15885chr19:13960875-13961655CD4_Naive_Primary_7pool
SE_17782chr19:13943266-13962691CD4p_CD25-_CD45ROp_Memory
SE_24646chr19:13960770-13962750Colon_Crypt_2
SE_27158chr19:13957065-13962903Esophagus
SE_27768chr19:13949302-13963575Fetal_Intestine
SE_28760chr19:13949189-13965110Fetal_Intestine_Large
SE_29787chr19:13956506-13962940Fetal_Muscle
SE_34630chr19:13946176-13967046HeLa
SE_36667chr19:13959473-13965372HMEC
SE_37011chr19:13948733-13965296HSMMtube
SE_38128chr19:13956463-13965113HUVEC
SE_39105chr19:13961475-13962948IMR90
SE_41122chr19:13956563-13963049Left_Ventricle
SE_42413chr19:13956569-13963420Lung
SE_44426chr19:13956507-13962882NHDF-Ad
SE_45089chr19:13960639-13964642NHLF
SE_46491chr19:13955521-13964784Osteoblasts
SE_49032chr19:13957052-13962760Right_Atrium
SE_49472chr19:13960823-13962773Right_Ventricle
SE_51833chr19:13960791-13963307Skeletal_Muscle_Myoblast
SE_54944chr19:13956487-13963104Stomach_Smooth_Muscle
SE_56033chr19:13960695-13963675u87
SE_58196chr19:13960880-13961346VACO_9m
SE_58196chr19:13961368-13962715VACO_9m
SE_63613chr19:13960696-13963563HSMM
SE_68219chr19:13949152-13977449TC32
SE_68559chr19:13949281-13977291TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191396120013961600
Enhancer Sequence
TGCTCATTAA GTGTTAGCTA GTTTGGGAGG TCGGCAGGGG TGGGGAGGAT GCAAAAAAGC 60
CCTCATCACA GCGCTCCTGA CAGCTCCCGC CAGGCCAGCT CCCCAAATCC CTTAGGAAAA 120
TGGCCTCGAC CTCTCAGCTG CAACTCTGGC CCAGCCGCCA TCTCCTGACC TGACCGCCCA 180
CTTCTGGGGA GCCCCGGTGG GTCTGGATTG GAGAGAGCCA CCCTCAGCCC TCCCCACCTT 240
CATTGGACCA CAGCTGTCTC CTTCACCATC ACCTCCGTGC CCACCAGGAT TACAGGCCTG 300
ATCTGAACCC CTAATCTAGG GAAGACTACG GAGTCCCAAA ATCCCTCTTA GCGCGCACCC 360
CGGCCTGAGG CTCGAACCCA GGTCCGCGCT GGAGGGCGGT GGCGGTTGCC GAGCAACGCG 420
CTGTTTGTTG GCGCGGGGGG CGGGGCCGGG GCCGGCGCGC GGTGACTCAC CGCGGCGTGA 480
TGCGGACGGG CGCGGCGCCC AGCAGCCTGG CCGGCGGCCC GATCTCGGCT GGCCTCGGCG 540
TCCGGAGGGG CCCGGCGGCG GGGGCGCCTT AGCCCCCAAG TGGGCGCCGG AGGCCCGTGG 600
GGAAGCGGCG GAGCAGGTCC CGGGCTCTCG GACTCGGTTC GAATCCCAGC CCTGCCTCTT 660
ACTCTTGACT CTTGATCTGT GACTTCAAGG CTCCTTGCCT CAGTTTACCC GTCAGTAAAA 720
GAAGCGACAC TGGAGGGTGC AGTAACCCAC CACTGGCATT TAAAGCAGCT GAGATGATCA 780
CGCAGTGACA CTGCGGGGCA GCAAGTTTGG GACACCCAGA TTCTGCACGT GAATCTCCTG 840
TGTTAAACTC TGCAACCTCA CGGAGAATCA ATTTCCGCAT CTGTTACAGG GCAGTAGCAA 900
GAACAAACAC CCTGCCTCTC GGGTGGTTTG AGAATCCCGT GAATTCATAG TGAGACAATG 960
CGTGGCACAT TTCAGTACCA TGTCTGCTGC CCCACGGAGG GACGGGATGT AGGAGGTTTT 1020
CTCTGTGGTC CGAGCTCAGG AGGGCAAGGA GGTGAGGGCA AGACTGGAAC CCCTAGAAGT 1080
GGGTGGCAAG TCACAGGTCC AGGGCAGGGT GGCATGACCA TGGCTGCAGA GGCCCCTATC 1140
CCGAAGCTGG CTCACAGCAC CTGCTGCGGG CAGGCAGAAG GGGGGCCTGG GGGTGAGTCA 1200
CCGCCCAGCA ATGAGGCTTG AGTCACACAG GGCGGGGTCC CCCGTTAGCC CCCCCAGCTG 1260
CTCCCACAAA GGCCCTTTGA GAAGAGTTCC CCACCCCCTA CTCCCACCCC CTAGGCCCTC 1320
TCTAGGGGTG GGCTGTGGGG CCGAGGCCCT GCTGGGCTGC CCCCAGGAGC CCGGCCTGGG 1380
TCTGGGAGGC GCCAGCCAGT TTCAGCCATG TCTGTGAAAA GTCACCATAG GAAGCTGGGT 1440
GTCCCCCGGG GAGGGGGCTT CCAGGCTGCC TGAGTCACTG GAATGGTGGA GGGTCACACG 1500
CGCAGGGCCC ACGCACACAG CGGGCAAATT GAGTCAGACT GTCTGGTGGG GCGGGCAGGC 1560
CAGGACGCTT CGAGTCAGGC TGAGAAGGAA ACCTGGGAAG AGACATGGTT CTTCCAAGCC 1620
TGTGGCCTCT GGCAGAGAAA GAGGGTGCTT GAGGGCACAT ATGGTGGGTT TCACCACACC 1680
TCCTGCCTAG GCCTCCCCTC CTTGCCTGCC CCGAAACAGT CTCCCCCACC TTTCTATCCT 1740
TCTTAAACTT GGAGTGAGAA GGACAGCAAG CTGGATGGGA TTCCAGGGAG GCACTCTACT 1800
AGCGGAAGAA TTGAGATTTT TTTTTTTAAT 1830