EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS165-05931 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr17:17597080-17598830 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr17:17598160-17598171GCCCCGCCCCC+6.02
KLF5MA0599.1chr17:17598160-17598170GCCCCGCCCC+6.02
KLF5MA0599.1chr17:17598139-17598149GGGGCGGGGC-6.02
SP1MA0079.4chr17:17598157-17598172GAGGCCCCGCCCCCT+6.59
SP4MA0685.1chr17:17598157-17598174GAGGCCCCGCCCCCTGG+6.29
TFAP2CMA0524.2chr17:17598537-17598549TGCCCTAGGGCA+6.92
TFAP2CMA0524.2chr17:17598537-17598549TGCCCTAGGGCA-6.92
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00905chr17:17594417-17599379Adrenal_Gland
SE_02229chr17:17595190-17599447Aorta
SE_02900chr17:17595277-17599403Bladder
SE_03155chr17:17595143-17597871Brain_Angular_Gyrus
SE_03155chr17:17598177-17598933Brain_Angular_Gyrus
SE_09034chr17:17596487-17597741Brain_Mid_Frontal_Lobe
SE_09034chr17:17598197-17598793Brain_Mid_Frontal_Lobe
SE_23508chr17:17594384-17598918Colon_Crypt_1
SE_23959chr17:17596267-17598838Colon_Crypt_2
SE_24961chr17:17596228-17598893Colon_Crypt_3
SE_26187chr17:17596287-17601342Duodenum_Smooth_Muscle
SE_26567chr17:17594663-17599474Esophagus
SE_28394chr17:17594411-17599671Fetal_Intestine
SE_29302chr17:17594492-17599795Fetal_Intestine_Large
SE_30808chr17:17594565-17599192Fetal_Muscle
SE_31385chr17:17592956-17599492Gastric
SE_33725chr17:17593502-17598845H2171
SE_33924chr17:17592560-17599542HCC1954
SE_34327chr17:17592369-17599360HCT-116
SE_36431chr17:17593663-17599189HMEC
SE_42083chr17:17594083-17599001LNCaP
SE_42180chr17:17594201-17604768Lung
SE_43483chr17:17594570-17597916MCF-7
SE_43483chr17:17598056-17600741MCF-7
SE_45144chr17:17596540-17599005NHLF
SE_46499chr17:17596499-17600278Osteoblasts
SE_47257chr17:17592191-17603274Panc1
SE_47490chr17:17596063-17599395Pancreas
SE_48869chr17:17594354-17599624Right_Atrium
SE_49608chr17:17596290-17599403Right_Ventricle
SE_50171chr17:17593988-17599544Sigmoid_Colon
SE_53329chr17:17594565-17599568Spleen
SE_54742chr17:17595926-17603895Stomach_Smooth_Muscle
SE_57229chr17:17596160-17599008VACO_400
SE_57532chr17:17596693-17598758VACO_503
SE_63253chr17:17584631-17604117GLC16
SE_65592chr17:17593958-17606061Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr171759747917598220
chr171759860017598800
Number: 1             
IDChromosomeStartEnd
GH17I017689chr171759264217604766
Enhancer Sequence
CAGGCCTGTG GTAGGGGGAA GGGAGAGGAA GGAACGGGAG ACCAGGCCAT TGCTCTGGGC 60
CAGAGATCGG CGGCTGGACC AGCCCGGGCT GGGCGGCCGG GAAGTAGCGA GTGCCACTAC 120
GTGTGGACAG GCATCTGGAG TCACAGCCTG GCCGAGTCCC AGCTCTGCCA CTTCACTCCT 180
TAACAGATCT GGGCTTGTTT GCCCACCTAA TCTGGGCAGT CATTCACACG TAGGACTCGC 240
TGGCTTAGGA GGAGAGTCAC CTGTCCTGGC CCAGTCAGTG TCTGCTCTCA TCCTACCCTT 300
GTCCCGTCAT TGCTGGCAGG ACACAGAATC AAAGGGATTC AGGGTCTCCT GGGAGCTGCT 360
AGCCTTGCCG GGTCTCCTGG GAGGGCAGCG ACTTCTGCTT AGATCTGTGG GCACTTTGGA 420
GTCTTTGACC GGGGAGGCAG CCGTGCTGAG GGGAAACGGG TTCTCTGCCC AATAACGGAT 480
GCCTGGGGTG TAGGTGGGCA GAGGCTGGCA TCAGGCCTGA GGAACCAAAC TGCCCCCTCC 540
TCGTCGCGGT GGAGACGCAC GAGGTGCGGG GAGGAACATA GCCAGGAAGA CGGGCCTTCC 600
TGTGGGGAGG GAGGGGCATC TTTTCTGGGG TGTGAGTCAC ATTCTGGATC CCAGCGAGGG 660
CAGCCCCCAA CCTGGCCCAC CTCTCAGAGG GCTGGGAGGG CCCGGGCCTC GAGGAAAGGC 720
ATAGGTAGGA GCTGTCAGGC CAGACGCCCG GGCAGCTCCA CGCTCGCCTC CGAGGCCATT 780
TCCTTTCCTC TCTCCCCGAC CTCGAGAAGG GGCGGCGAGA GGGCAAATGC CCGCGCTTCC 840
TGCCGGTCCC GCCCCTCCCC GCCCGCGGCG CCCACCATCT TGGCCGCGCC GGAGCCTCCT 900
CCGCGGTGGC GTCCCACAGG CCGCGGTCGG GGCCCGCGAC GCCGACGCCG GGAGGGGGCC 960
CGGGACCTTC GGGGCGCTGA GGCCAGGCGG GGGGCGAGGC GGGGCGGGCC GCTCGCGTCG 1020
CCATGGCAGC GCCCGGCCCG GCATGCTTCG CGGGGCCGCG GGGCGGGGCG GGGTGCTGAG 1080
GCCCCGCCCC CTGGCGGATC CCGGGTCTTT TTCCGGGAAC GCGGGGGCTT CCAGTCCCAG 1140
CGTTGCGGCC GGCGCTTGCG GGTTACCGGG CCAGGCGGCG CGCATCTCTG GGCCTCGTTC 1200
TCCCACTCCC TGGATGTTTG GGGATAATGA AAGAGAGTCT GTGCGGGTTA GCCTCGGGAC 1260
GGGCTCTGCT TACCGAGCCC GGCAACCCCA CGGCAGGGGC CTCGGGAAGC CGCTTCCGAG 1320
GGCCAGGATA ATGGGGAGAC TGGACCCCTA CCGCTTGGGG GCTATTAAAA GTGGAGGCCA 1380
GGCGGCCTCT CAGCTGCAGT CTCTGGGTCT CGAGCTCTTC CCCGGAACTG TCCATGGGTC 1440
AGTGAGGACC TACCCTTTGC CCTAGGGCAG GAGAAAGAAG GGGGCCGGGA CTGCACACCT 1500
CACCCGGTCC AGGCCTGGAC CCTGCAACCT CGGCCGGCCT CCCTCCAGCC CAGGAGCACA 1560
GGCCTCCCCT AGTTGGCAGT CGTTGGACTG TCTGGCTGGG AGGCACATTC CTACCTCCTG 1620
AGCTCGGGCA CCCCGCCTGC CCTGGGGGAG CCTCTTCCAG AACTTTGCTG CCAACACTGC 1680
CCTGTCCCCA CCCGGCCTTC TCGTGCCCTA AGTCCCTAGT TACTACTCCA CAGCCGCCTT 1740
CTTTCCCCTG 1750