EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-24018 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr17:17596320-17598910 
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
ATGCGGGTAT TTATTTTTCT TTGCCTGTGA AAGCCCTGTT TTCGCTCAGG CTGTGTAGGG 60
CTTCCCGACA CTGCCATGGG TGCGCACATC TGCACACTCT GGGGTGCCTG CCATGCAGAG 120
GCATCTGCCC AGGGTGGGCA CTGAGGGCAT CCACCATGTG ACGCCCCCGT GCAGCCTGTA 180
AGCTCTCATC ACAGTGCCTG GGATACCTGG GAGTCCCCAG AAAGAGTGAG GATGGGTGAG 240
GGCCATGAAA CCAGGGCATC ATTCCTCCAC CTCCTCTGAT CAGGCCCTCC TGGTCCCATT 300
CATCTCCTTA TCTCCTGGCA GCCAGTGGGT TGCTGGGAAG GCAGGGGCAG CCTTCCTGAT 360
TGACAAACAA AACAAGCTTG ATCACAAAAG GAGAGGGGAG ACTGGCTGGG CCTCTCCAGC 420
TCCCCTCCCC GTGCCCCAGG CATCTTTCTT GCTCCACCCA ACTGGCACCC TACATTCTAA 480
GATGCTGCGA GGGGGCTCCA AAGCCATTGT CGAAGGTCAG GCCACCCAGG CTAGGAGCCC 540
CTTGCACTGG GGAGGTGGAT TCAAGGAGTG ATGGGGTTGC CATGAGGCGG CGCTTGCTGC 600
AATGGCCGCC CCTCCTTCCC TTCAGCTGGC TGGGCAGGCA GCTTGGAGAG GAAGCCAGGC 660
GGCAGGTAGC TGAGAAAGAC ATCGGATCCA GGGGGAGCAG CAGAGAAAGC AAACAAACAG 720
GGCTTTGTGT GGCTGCAGAT TGGCGGCTCA GAAGGGAAGC CAGGCCTGTG GTAGGGGGAA 780
GGGAGAGGAA GGAACGGGAG ACCAGGCCAT TGCTCTGGGC CAGAGATCGG CGGCTGGACC 840
AGCCCGGGCT GGGCGGCCGG GAAGTAGCGA GTGCCACTAC GTGTGGACAG GCATCTGGAG 900
TCACAGCCTG GCCGAGTCCC AGCTCTGCCA CTTCACTCCT TAACAGATCT GGGCTTGTTT 960
GCCCACCTAA TCTGGGCAGT CATTCACACG TAGGACTCGC TGGCTTAGGA GGAGAGTCAC 1020
CTGTCCTGGC CCAGTCAGTG TCTGCTCTCA TCCTACCCTT GTCCCGTCAT TGCTGGCAGG 1080
ACACAGAATC AAAGGGATTC AGGGTCTCCT GGGAGCTGCT AGCCTTGCCG GGTCTCCTGG 1140
GAGGGCAGCG ACTTCTGCTT AGATCTGTGG GCACTTTGGA GTCTTTGACC GGGGAGGCAG 1200
CCGTGCTGAG GGGAAACGGG TTCTCTGCCC AATAACGGAT GCCTGGGGTG TAGGTGGGCA 1260
GAGGCTGGCA TCAGGCCTGA GGAACCAAAC TGCCCCCTCC TCGTCGCGGT GGAGACGCAC 1320
GAGGTGCGGG GAGGAACATA GCCAGGAAGA CGGGCCTTCC TGTGGGGAGG GAGGGGCATC 1380
TTTTCTGGGG TGTGAGTCAC ATTCTGGATC CCAGCGAGGG CAGCCCCCAA CCTGGCCCAC 1440
CTCTCAGAGG GCTGGGAGGG CCCGGGCCTC GAGGAAAGGC ATAGGTAGGA GCTGTCAGGC 1500
CAGACGCCCG GGCAGCTCCA CGCTCGCCTC CGAGGCCATT TCCTTTCCTC TCTCCCCGAC 1560
CTCGAGAAGG GGCGGCGAGA GGGCAAATGC CCGCGCTTCC TGCCGGTCCC GCCCCTCCCC 1620
GCCCGCGGCG CCCACCATCT TGGCCGCGCC GGAGCCTCCT CCGCGGTGGC GTCCCACAGG 1680
CCGCGGTCGG GGCCCGCGAC GCCGACGCCG GGAGGGGGCC CGGGACCTTC GGGGCGCTGA 1740
GGCCAGGCGG GGGGCGAGGC GGGGCGGGCC GCTCGCGTCG CCATGGCAGC GCCCGGCCCG 1800
GCATGCTTCG CGGGGCCGCG GGGCGGGGCG GGGTGCTGAG GCCCCGCCCC CTGGCGGATC 1860
CCGGGTCTTT TTCCGGGAAC GCGGGGGCTT CCAGTCCCAG CGTTGCGGCC GGCGCTTGCG 1920
GGTTACCGGG CCAGGCGGCG CGCATCTCTG GGCCTCGTTC TCCCACTCCC TGGATGTTTG 1980
GGGATAATGA AAGAGAGTCT GTGCGGGTTA GCCTCGGGAC GGGCTCTGCT TACCGAGCCC 2040
GGCAACCCCA CGGCAGGGGC CTCGGGAAGC CGCTTCCGAG GGCCAGGATA ATGGGGAGAC 2100
TGGACCCCTA CCGCTTGGGG GCTATTAAAA GTGGAGGCCA GGCGGCCTCT CAGCTGCAGT 2160
CTCTGGGTCT CGAGCTCTTC CCCGGAACTG TCCATGGGTC AGTGAGGACC TACCCTTTGC 2220
CCTAGGGCAG GAGAAAGAAG GGGGCCGGGA CTGCACACCT CACCCGGTCC AGGCCTGGAC 2280
CCTGCAACCT CGGCCGGCCT CCCTCCAGCC CAGGAGCACA GGCCTCCCCT AGTTGGCAGT 2340
CGTTGGACTG TCTGGCTGGG AGGCACATTC CTACCTCCTG AGCTCGGGCA CCCCGCCTGC 2400
CCTGGGGGAG CCTCTTCCAG AACTTTGCTG CCAACACTGC CCTGTCCCCA CCCGGCCTTC 2460
TCGTGCCCTA AGTCCCTAGT TACTACTCCA CAGCCGCCTT CTTTCCCCTG GTCTTTCTCT 2520
CTCTCTTTTT TTTTTTTTGA GCTAGAGTCT CCCTTTGTCG CCCAGGCTGT AGTGCAGTGG 2580
CGTAATCTCC 2590