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

TagContent
EnhancerAtlas ID
HS176-25959 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr3:39188210-39189920 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr3:39188530-39188550ACACAAAACACACACACACA+6.71
RUNX1MA0002.2chr3:39189751-39189762AAACCACAAAC-6.02
ZNF263MA0528.1chr3:39188785-39188806TCTGCTTCCTCCTCCTCCTCC-6.43
ZNF263MA0528.1chr3:39188788-39188809GCTTCCTCCTCCTCCTCCTCC-9.27
ZfxMA0146.2chr3:39189388-39189402GAGGCCGAGGCCCC-6.31
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00534chr3:39187077-39197631Adipose_Nuclei
SE_01089chr3:39187508-39190600Adrenal_Gland
SE_01899chr3:39187322-39196765Aorta
SE_02320chr3:39187493-39196198Astrocytes
SE_03014chr3:39187741-39190548Bladder
SE_04302chr3:39187580-39195097Brain_Anterior_Caudate
SE_05565chr3:39187535-39197818Brain_Cingulate_Gyrus
SE_06185chr3:39187142-39197857Brain_Hippocampus_Middle
SE_07580chr3:39187284-39196241Brain_Hippocampus_Middle_150
SE_08206chr3:39186982-39195061Brain_Inferior_Temporal_Lobe
SE_10149chr3:39186779-39195996CD14
SE_14356chr3:39187118-39191048CD34_Primary_RO01549
SE_17247chr3:39188355-39190934CD4p_CD225int_CD127p_Tmem
SE_18872chr3:39187113-39196177CD4p_CD25-_Il17-_PMAstim_Th
SE_19278chr3:39187136-39196336CD4p_CD25-_Il17p_PMAstim_Th17
SE_23377chr3:39187613-39190524Colon_Crypt_1
SE_23920chr3:39187798-39190475Colon_Crypt_2
SE_24797chr3:39187657-39190081Colon_Crypt_3
SE_26868chr3:39187409-39196585Esophagus
SE_31506chr3:39187425-39190678Gastric
SE_35162chr3:39188481-39190214HeLa
SE_36770chr3:39187856-39190350HMEC
SE_37186chr3:39186804-39195747HSMMtube
SE_38092chr3:39187171-39195921HUVEC
SE_40501chr3:39188054-39190602K562
SE_40691chr3:39187355-39196752Left_Ventricle
SE_41653chr3:39187913-39190606LNCaP
SE_42157chr3:39187438-39196764Lung
SE_45141chr3:39187656-39190533NHLF
SE_46489chr3:39187606-39195364Osteoblasts
SE_47666chr3:39188511-39189839Pancreas
SE_48424chr3:39187382-39196729Psoas_Muscle
SE_49175chr3:39187672-39190712Right_Atrium
SE_50193chr3:39187407-39196676Sigmoid_Colon
SE_51558chr3:39187056-39196628Skeletal_Muscle
SE_52456chr3:39187337-39197976Small_Intestine
SE_53827chr3:39187396-39196382Spleen
SE_55403chr3:39187983-39191324Thymus
SE_58072chr3:39188449-39189462VACO_9m
SE_58072chr3:39189509-39190535VACO_9m
SE_60385chr3:39186669-39195737Ly4
SE_62971chr3:39182508-39196204Tonsil
SE_63844chr3:39187601-39190894HSMM
SE_65440chr3:39187335-39197020Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr33918860039189000
Enhancer Sequence
AGCCTGGAAT AGGAATGAGA AGGCTCTAAG TGGCAGGCAG GCAGCAGCAG GTGGACTTCC 60
AGCCAGGATC ATCATCCCTC CCACTTACCC TCCAAGGCAT CCCAGACCCT GGCCTCTGCC 120
CTCCAGCCCT GCCTGTGGAG CTCTGTGTGG GGGAGGGCAC AGTCTCCAGG AGGATCTCTG 180
CACAAGACAC AGCACCTCCC TCCCTCCAAA CTAATGTGCA AATCCACAGC CTGATGCTTC 240
AAACTCCCAC CTCTGCCCAA AGCCTTCCCA GGCACCAGGC ACCTTCCCCA CTACCTCCTA 300
CAACACACAC TTACATACAT ACACAAAACA CACACACACA CACACACACA TGCATCCACA 360
CCAGCAGGGG AAGGAGGCAG ACAGACCAAC AGATGGACTG ACAGACCTCA GCCTGGTCTC 420
ACTCATTCCC CGACAGGAAT CCTGGCGCTG ACTCACAGGC TGGGTGATTC ACACAGCTTG 480
CATCTGTGTG CCTGTGTGTG TGTGTGTGTG TGTGTGTATG TGTGTGTGTG TACGCCCTAC 540
AGCCCGCACA GCCCGCACGG CCCTGGTATG GTGGCTCTGC TTCCTCCTCC TCCTCCTCCA 600
GCACATCCAA ACAGGCACGC CACTCTGCAC ACAGGCAGGG CTGCGGGCCC TTGCTCCAGG 660
CTAGCCAGGC ACTCTGGGGA ACAGGCTGGC TTTGACGTTG GCCTCCATTC CTAGACGGAG 720
TAGTTTCTGA GCCCTTCCCC TCCCGGTGTG GGAGCTTCTC AGACTTTCCC TTAGAAACCC 780
CCGCTCCACT GTCAAGAAGT CTCCTGCCTC CAGGCCTGTG TGACCACAGC CACTAAGGCT 840
GTCTCTTTAA CATCTCATTT GATCCTAATG TCCAAAGTCT CTCCTGTCTG TGGCTTCGTG 900
ACATGGAGCA CCCCACAACA CAACACTGTC TCCCAAGTGA GAGTCTCAGC CCTCAGCAGA 960
AGCATAACCA GAGACTCCCA CAGCTGGCTG GCCTTATCCA AGCAGAAGAG ACTTGGGGCT 1020
CATTCCCTGG AATGCTTCAG CAAATAAGGG TCCTTCCCAA GGTTTGGCAA GCCCCAGAGG 1080
ACTCAATCCC AAAGGCTGAG TACAGCTACC TTGTGTCTGT TGCTCCAGCT GGGCCTTCGG 1140
GGAGGTCACC AGGGGGAAAG GGAAAGGAAG TTGAAGCTGA GGCCGAGGCC CCAGTGCTGG 1200
GGAACCCTTC CCCCACTGCC ATCACAGGAA ATGAGAGAGA ACAGGAAAAA CCAACCAGAA 1260
GGCTGTCTTG GTCTCCTCTA CTCAGGTGTC CTTTCCAAAC ACTCCTTTGC CCTCTTCCCA 1320
GCCGCCTACA AAGTCCCCGA ATCCTGTAGA GTTTGCTGTC AACCTTACTA ACTGGATAAT 1380
GTTTACCCCA GGGACAGCCT CCCCTAGGCA AGCGTGAGAG AAGCAAGAAA ATCTCCCTCC 1440
CCAGCCAATC CCCCACCCTG GGCCTGGGGG AAGACTCACA GATGTTTCCG GGGGCTTCTC 1500
CGTGGGTAGT TTCTCAGGCT TGGCACCCCC CTCCCAGGGT CAAACCACAA ACAAAAACAA 1560
CCCAGCTCCC AGCTGACCAG CAGGTTCTCC CAGGAGGTGG GGGATTCATG ACCCAGAGGC 1620
AGGCATACTC ACATGTACAC ACATGCTCAG ACAACACGGA AACACACATA TGGACAAACA 1680
ACACCCACAC ATCCTGTCCC CATCGCATCC 1710