EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-09575 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr2:232525930-232528180 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF9MA0653.1chr2:232526387-232526402AACGACAGCGAAACT+6.17
NRF1MA0506.1chr2:232527094-232527105GCGCCTGCGCA+6.62
Number of super-enhancer constituents: 57             
IDCoordinateTissue/cell
SE_00956chr2:232526407-232527757Adrenal_Gland
SE_02118chr2:232526377-232527069Aorta
SE_02118chr2:232527143-232529172Aorta
SE_03344chr2:232526391-232526890Brain_Angular_Gyrus
SE_03344chr2:232527085-232527807Brain_Angular_Gyrus
SE_03959chr2:232526025-232528260Brain_Anterior_Caudate
SE_05028chr2:232525295-232528786Brain_Cingulate_Gyrus
SE_05842chr2:232525855-232541886Brain_Hippocampus_Middle
SE_06810chr2:232526262-232528302Brain_Hippocampus_Middle_150
SE_08041chr2:232526039-232528818Brain_Inferior_Temporal_Lobe
SE_08891chr2:232527332-232527579Brain_Mid_Frontal_Lobe
SE_10218chr2:232526051-232528836CD19_Primary
SE_11120chr2:232525439-232541839CD20
SE_12621chr2:232527269-232527559CD34_adult
SE_23069chr2:232526523-232527135Colon_Crypt_1
SE_23069chr2:232527174-232529137Colon_Crypt_1
SE_23744chr2:232526535-232527115Colon_Crypt_2
SE_23744chr2:232527187-232528498Colon_Crypt_2
SE_24686chr2:232526285-232528931Colon_Crypt_3
SE_26538chr2:232526205-232528305Esophagus
SE_27945chr2:232525107-232527993Fetal_Intestine
SE_28950chr2:232525098-232527996Fetal_Intestine_Large
SE_30147chr2:232526251-232527910Fetal_Muscle
SE_31275chr2:232526184-232527937Fetal_Thymus
SE_31583chr2:232525439-232526416Gastric
SE_31583chr2:232526504-232528553Gastric
SE_32771chr2:232526377-232527071H1
SE_32771chr2:232527132-232527917H1
SE_34301chr2:232526292-232532681HCT-116
SE_34676chr2:232526410-232529112HeLa
SE_40924chr2:232526289-232529202Left_Ventricle
SE_42371chr2:232526256-232528917Lung
SE_47005chr2:232526510-232527706Ovary
SE_47674chr2:232526568-232527040Pancreas
SE_47674chr2:232527155-232527662Pancreas
SE_48427chr2:232526298-232529035Psoas_Muscle
SE_48956chr2:232526514-232528579Right_Atrium
SE_49615chr2:232526571-232527117Right_Ventricle
SE_49615chr2:232527137-232527889Right_Ventricle
SE_50073chr2:232526351-232532740Sigmoid_Colon
SE_51193chr2:232525969-232528618Skeletal_Muscle
SE_52583chr2:232526367-232528470Small_Intestine
SE_53812chr2:232526183-232528459Spleen
SE_54893chr2:232526011-232532911Stomach_Smooth_Muscle
SE_55415chr2:232526518-232527790Thymus
SE_56815chr2:232526245-232528751VACO_400
SE_57401chr2:232526517-232527034VACO_503
SE_57401chr2:232527067-232527827VACO_503
SE_57994chr2:232526533-232527069VACO_9m
SE_57994chr2:232527107-232528619VACO_9m
SE_58398chr2:232468621-232552645Ly1
SE_60442chr2:232526263-232553020DHL6
SE_61093chr2:232461681-232552859HBL1
SE_61422chr2:232466061-232552901Toledo
SE_62587chr2:232525960-232546908Tonsil
SE_65285chr2:232526105-232528084Pancreatic_islets
SE_68691chr2:232526434-232528799H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr2232527400232527800
chr2232526700232527324
chr2232526400232526574
chr2232526611232527400
Number: 1             
IDChromosomeStartEnd
GH02I231660chr2232525334232533149
Enhancer Sequence
CACTGAATCA GACAGTGGCT GTACTGGAAG GTGGAAAAGA CTATTCGTCC TTTCGCGTCC 60
TTTAAGTACT TCTGTACTTA TCTCTGTGTG TCAGTTCTTC CACGTGGACC TGGTTATGAA 120
AGTTAATGCA CTTAAAACAG GGCCTGGCAT ACTGCAAACG GAAGGTGAAC ACTACCATTC 180
TTTCTTTCAA AAATTTCTAC TGGCCGGGCG CGGTGGCTCA CACCTGTAAT CTCAGCACTT 240
TTGGAGGCTG AGGCGGGCAG ATCACGAGGT CAATATATCG AGACCATCCT GGCCAACATG 300
GTGAAACCCC TTCTCTACTA AAAATACAAA AATTAACTGG GCGTGGTGGT GGGCGCCTGT 360
AGTCCCAGCT CATAGGGAGA CTGACGCAGA ATTGCTTGAA AGCGGGAGGC GGAAGTTGCA 420
GTGAGCTGAG ATCGCGCCAC TGAACTCCAG CCTGGGCAAC GACAGCGAAA CTCCGTCTCA 480
AAAACAAACT TCTACCAAGA ACTTGTATTA GTTTTATGGC TAAGGTTTGC TTTTAAACAT 540
TTTCTTGATC ATTGTTTTAC AGGAACATCT CTTTAATGGA AATTTTTAAA CTTATTTTTG 600
CCTCCCCCAA ATCCATAACC CCAATTTGAA GTAGAAAGTT GCAAACTATG GGGATGAATT 660
TGCGGAAGGG TATGTCTTTT CTTTTTCTAT GAACAACTCA GAATCACATC TCAAAAGGTG 720
TAGGCACTTT CAAGAACGCT TCATCCGCCC GCTTTAAGCA CGCGCACCGA CGAAAGAGTT 780
TGGGGAGCGA GCGCCTCGGG CTTCCCCGGA GGGGAATTTT CACCCCCGCC AGAGGAAGAG 840
GGCCCAGCTG CGCCATTAGC GCGTGCGAGG GAAAATGGAG GCTCCTGGTC CCACCCGCGC 900
ACCGGCGCCT GCGCCCTGGG CGCCCACCCC GGCCCGCGAG GCGGCCACGG CCGGAGAGAG 960
AGGGCAAGGG AACCAGTGCC GTGTCGCGCC CCACCCTGCG CCCGAGCGCA GTGCCGGCGA 1020
GCCCGGCTCC GGCCCTTGAG AGTCCGCTCC AGGCCGCTCC ACACCACGAG CCGCTCCGCA 1080
AGTTTGCAGC GCTCCGTGCT TTCCCTCCAG CCCTTTGTGT TCTAGCGCGC GTCGGAAGGA 1140
ACGCGGGAAC GCGCGCCGTG CTGTGCGCCT GCGCAAGGGT TCAGGCGGTG CGCCAAGCCT 1200
GGAGTCAAGA GTGGGCGAGG CTCTCGGCCG CTCCGCCCCG GGCCGCCTTC GCTCCGCCCC 1260
TCGCCCGCCA TTTCGTGCTC CGCCGCGTCT CCCGCGTCTG GGGCGCGGCT TCCGCGTGAT 1320
GGACGCCCGG AAGCCGGCAC AACAAATGCC CAAGCGCCAG GGCTTCGCTG TCTGCAGGTC 1380
CTTCCGCTGC CCGCGGAGCG AAGATGGCGC CTAGAGCTTG CAGCGTTGCC CAAATATGGG 1440
GGGAATTAGG CGCCTCTACC TCCTCAAGAA GGGTCTGCCG GCTGACCTCG GGGGTGTGCA 1500
CGTCCTTCTG TGTGCAGAAC CCTGGGGCGT GCGCCTTTCT GTATGTGCAC AACCTCGGAA 1560
GTGTGCGCAT ACCCTTGCTT ACACTCCCTA GCACGCACAC CAAAACTCTG GCATGCACGA 1620
ACCCGCGGGT TTCCATGTTT TCGTATGTGC ACGACCTCGA GGATGTACTT GGACCCGAGA 1680
ATGTCCGCAT TTGTGTTTGC ACAGGTCCGG GTGTGCACGG ACACGTGCAT TCAGGAATGT 1740
AGTGGTTCAC AGAAGCCGCT GTTTGCGCGG CCCGGGGATG TACGTGGACC CTCGAGTGCT 1800
AGCCCCGCCT CCGCTGTCTG TGGCCCGCGA ACACGATCTT GTTTCCGGCC TGTTTTGGAT 1860
TCATTTGCAC TTGCCCAGTT TACATGCAAA GCATAATCTG CCGACCACCC CAAGCAATTT 1920
TTAATCTTTC CTTCGTTCTT TCTTCACTGA TTTTTTGGCT CCTGCCCTGG ACCCAACTTT 1980
GCACTTGGGC GCACACGGTG ATAGTGACGC AGAGCATGAA GCCAGTGGGA GAAACGCCTA 2040
GAAATAGGCA GTTAGGACAA CCTGAGACCA CTGTGAAGGA GGCGCTTGGC TTGTCAATGA 2100
CAGGGGAAGC GGCCTGGAGG AAGCCGTGAG CCGAGACCAG GGCATGGGGT AGAGGGAATA 2160
GGGTAATGGG CCCAGGACTG TTTGGGGAGG CATTCAGTCT CATTTGAGAG GATGGTGGGT 2220
GGAAGCAGAG GAGGCAGGTC ATGGAGAGGA 2250