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

TagContent
EnhancerAtlas ID
HS007-17716 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr9:134608850-134610150 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr9:134609391-134609402TTCTTATCTCT+6.32
Gata1MA0035.3chr9:134609391-134609402TTCTTATCTCT+6.32
Gata4MA0482.1chr9:134609392-134609403TCTTATCTCTC+6.32
JUN(var.2)MA0489.1chr9:134609237-134609251ATGACTCATCTCTA-6.08
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00686chr9:134608884-134613190Adipose_Nuclei
SE_04525chr9:134608863-134612853Brain_Anterior_Caudate
SE_09150chr9:134602020-134613269CD14
SE_10404chr9:134599070-134613095CD19_Primary
SE_10884chr9:134591844-134615384CD20
SE_12120chr9:134606082-134613193CD3
SE_14804chr9:134606083-134613399CD4_Memory_Primary_7pool
SE_16701chr9:134601791-134611990CD4_Naive_Primary_8pool
SE_17150chr9:134606063-134613218CD4p_CD225int_CD127p_Tmem
SE_17952chr9:134601452-134615329CD4p_CD25-_CD45ROp_Memory
SE_18769chr9:134601534-134615309CD4p_CD25-_Il17-_PMAstim_Th
SE_19472chr9:134602036-134615436CD4p_CD25-_Il17p_PMAstim_Th17
SE_20363chr9:134601294-134613216CD56
SE_22914chr9:134601848-134613223CD8_primiary
SE_27117chr9:134606526-134611391Esophagus
SE_30786chr9:134606415-134610798Fetal_Muscle
SE_31710chr9:134608376-134613068Gastric
SE_32578chr9:134599803-134613266GM12878
SE_33628chr9:134605461-134610903H2171
SE_36750chr9:134606498-134610470HMEC
SE_36915chr9:134602036-134616473HSMMtube
SE_38234chr9:134607748-134613138HUVEC
SE_40722chr9:134608773-134610234Left_Ventricle
SE_42566chr9:134606682-134613188Lung
SE_44033chr9:134608797-134610392MM1S
SE_49262chr9:134608245-134611154Right_Atrium
SE_50405chr9:134606039-134613162Sigmoid_Colon
SE_52037chr9:134606112-134612282Skeletal_Muscle_Myoblast
SE_52732chr9:134605999-134613197Small_Intestine
SE_54202chr9:134601963-134613163Spleen
SE_58352chr9:134520171-134620333Ly1
SE_58881chr9:134579557-134620273Ly3
SE_60383chr9:134599961-134620084Ly4
SE_60991chr9:134494570-134620113HBL1
SE_61989chr9:134594251-134616125Toledo
SE_62218chr9:134495530-134621458Tonsil
SE_63796chr9:134606096-134612370HSMM
SE_64992chr9:134606662-134610348NHEK
SE_66603chr9:134608729-134612181Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9134609553134609906
chr9134608936134609538
Enhancer Sequence
GATGGGGAAA ATAAGCCCCA GGAAAGGGTA AGAATCACCC AAGGACACAA CTAAGATGTT 60
CTCAAACAGA TGACCAGAAA CTAAGATGAC TGGCCTGCTG GATGACAGAT CCCTTAATAA 120
TTCACAAACG GTGGGTTTTA TTTATTTACT CATAAAACAG CCTTTGGGGC AAGACGGGTG 180
ACGAGTCAGA GGAACACCTG TCCCGGCGGC GAGGCGGCCG CGGGGTGGGG CAGGCGGTGG 240
GTTGTCAGGC CTCTCCTCTT TCCAGAGCGT GATCTTATCC TGGCCATGGG GAACACGCTC 300
AGCTGGCCTG AGGTAAGACC CAGCCTGGCA CTCAAGGCAA TCTCCAATCC GGGCTACTTT 360
GGGAGACATT TTTCTGCAAG CTCACACATG ACTCATCTCT ACAGACCTCC TATAAGGTCT 420
CTTGGCTACA AGGAATCCCA TTCAAACCGC CTCTGCCAAC AGCTGCTCTG GAGACCAGGA 480
AACATTTGGG GTTGCTGTGG TTGATTTTTC TAAAAACACA CTTAGCTGGC ATTAGTGCTA 540
TTTCTTATCT CTCTACAGCA CTGTTAATGT GACTAGTATT ACGAGTATCA GACGCAGTCT 600
AAAGACTGTA GTGAGCCTCC CTTAATTTCA TTGGTAGATC TTTTTTTTCA AAGATCAGAA 660
AAGAGATTGA GAAGCCTGAA GAATTAAGAT GGAAAGCTGT GTCCCCAGCA ACCAGGGAGG 720
CTCTAACCAG TGCTCTATAA AGGCAAGAAA GGGGGCCGGT TCCCCATTCC ACTTCTCCAG 780
GGCATGACCT TGGGCAAACA ACCAAATTTC CCTGGGCCTT AGCTGCCCTG AGGGGCAAAA 840
GAGGGATACT CCGCCCTGCC CTCACCCCCT GGGCTGTTGT GAGGATGAAA TGAAATGAGG 900
TAGTCTATAA ATGCATTCTG AAAACCACAG GAAATTGCAG AGATGTTCAA GATCGTTCTG 960
ATTCTACCCC TGGACTGTGG CCTCCAGGGA CAGGTTCCTG CTGGCTCCCT GCCACGAGGC 1020
ATCACTTGGT GTTTGCCAAC AAGGAGGCAC TCAGTAAGTG TTAAAACGGG TGAGTGAAAG 1080
GAGGCAGAGC AGGTGCCATC AAAATGTCTC ATTGCTTGAC TGAGTATACT TTGACGACAA 1140
AAATTCCTAA CTATGGAGGA AAAAGGAAGT ACAAATTTGA CGAGTTTAAA ATTGATCGAA 1200
ATACAATGAC TGCCAATCTA AGAGGACCTC TTTCTCAGGC CACAAAAATG AGTAGCCCTA 1260
CATCATAGGG CCTGTACTCT TAGTATCTGT TCTGAGAAAA 1300