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

TagContent
EnhancerAtlas ID
HS092-22056 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr18:74768330-74769610 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf12MA0742.1chr18:74768897-74768912GACCACGCCCACACC+6.3
MecomMA0029.1chr18:74769283-74769297CAGACAAGATAATC+6.02
SP1MA0079.4chr18:74768895-74768910CTGACCACGCCCACA+6.53
SP3MA0746.2chr18:74768897-74768910GACCACGCCCACA+6.21
SP4MA0685.1chr18:74768895-74768912CTGACCACGCCCACACC+6.47
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_02301chr18:74765615-74769291Astrocytes
SE_03187chr18:74768362-74769202Brain_Angular_Gyrus
SE_03925chr18:74762993-74769676Brain_Anterior_Caudate
SE_04802chr18:74760877-74769887Brain_Cingulate_Gyrus
SE_05798chr18:74762601-74769949Brain_Hippocampus_Middle
SE_06694chr18:74761722-74769901Brain_Hippocampus_Middle_150
SE_07751chr18:74762635-74769942Brain_Inferior_Temporal_Lobe
SE_09139chr18:74763390-74771272CD14
SE_10547chr18:74764261-74769635CD19_Primary
SE_11015chr18:74762704-74785115CD20
SE_12115chr18:74764048-74769337CD3
SE_13103chr18:74765655-74769275CD34_Primary_RO01480
SE_13673chr18:74763883-74769625CD34_Primary_RO01536
SE_14260chr18:74763782-74769393CD34_Primary_RO01549
SE_15038chr18:74763788-74768613CD4_Memory_Primary_7pool
SE_15651chr18:74764917-74768462CD4_Memory_Primary_8pool
SE_16468chr18:74765452-74768807CD4_Naive_Primary_8pool
SE_17255chr18:74765526-74769066CD4p_CD225int_CD127p_Tmem
SE_17959chr18:74762819-74769776CD4p_CD25-_CD45ROp_Memory
SE_18700chr18:74763026-74769998CD4p_CD25-_Il17-_PMAstim_Th
SE_19374chr18:74763980-74769767CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74763553-74769915CD56
SE_21261chr18:74765053-74769077CD8_Memory_7pool
SE_22307chr18:74763553-74769856CD8_primiary
SE_25341chr18:74763020-74769931DND41
SE_25885chr18:74765504-74769852Duodenum_Smooth_Muscle
SE_26884chr18:74767691-74769645Esophagus
SE_30168chr18:74765890-74769751Fetal_Muscle
SE_34994chr18:74765147-74769503HeLa
SE_39197chr18:74765915-74769297IMR90
SE_41189chr18:74765691-74769624Left_Ventricle
SE_42218chr18:74764253-74769817Lung
SE_47137chr18:74764303-74771360Panc1
SE_48227chr18:74765445-74769622Psoas_Muscle
SE_49182chr18:74767754-74769611Right_Atrium
SE_50626chr18:74764327-74769788Sigmoid_Colon
SE_51089chr18:74763882-74771359Skeletal_Muscle
SE_52417chr18:74764263-74769800Small_Intestine
SE_53332chr18:74764213-74769843Spleen
SE_58547chr18:74756065-74865317Ly1
SE_61817chr18:74764079-74793826Toledo
SE_62620chr18:74763866-74793718Tonsil
SE_65574chr18:74763757-74769532Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr187476865574769369
Number: 1             
IDChromosomeStartEnd
GH18I077051chr187476336674770955
Enhancer Sequence
TGAATTATTT CTCCGTCCCT TTGAGACATC GGCCCTTTCC TGGCCTCTTG CTCAGTTCAC 60
TGCCCAGCTT TGTCTTCTCG AAGGACCCAG GAGCCTTTGA AATGTAACCA ACAAGGAAGA 120
TAACACCCTC AGCTCCCAGT CCCTGCGGGA GGCAGGGGCC TAACTGTGGT AAGCGCTAAT 180
CTGCAAACAT TGCTGGCCTG ACTGCACCAA CCGGCCTCCA TCCGATGTCC TCCAGGACTC 240
TCCCACCAGC TCACCCCAGT GCTTAAAAAC CCTCCCGCCT TTCGTTTCAG CAGGGTGGAG 300
TTCAGCTCGC TCTCTCCTAC TGCAATAGTC TGGGATACGT CTTCCCTGCC TGTCTCACTC 360
TCCCTGGGGT AACTTTTCTT TGACACCACT GAGTCCTCCC AGCAACCTGC AGCTGAGCAC 420
ACAACCCCCC TCTGCACAGG GGAACCGAGT CCACAGTCCT AACTACCAAA TGACATGGCC 480
TCACTAAAGT AACTCCTAGA AGCCGAGACC TTTGTCCGAC AGCTCTCAGG AGAGGCTGCC 540
GAGGAGAACC GGCTTCCCAC GTGCCCTGAC CACGCCCACA CCCACGGCGT GAGATTTCAC 600
CACTCAGCCG CTGAGAAGCA GGGGGTCTTT GGCCCAAAAC AAACATCCTC TGAGACGGGA 660
AGGAGGCATG TCCCCCAAGA ACTGCCTGGG TACTACAATG AAGCAGGGTA AATATTCAGA 720
AGTGTGTTTG GGTTTTTAAT GATATAAAGT ATCATTAACA TTCACTTCAA CGCACAGAGG 780
AGAAGTAACT GTTACAGTGT TTGTTTTCAC ATCTGTCAGA CAGACATGAG AACTGCCCTG 840
CCCCTCAAGG AACCAGCTGC GGTCTCCCTG GCTGGCTGGG AGCACTGGGC TCCGATCCTG 900
CTCCTGAGTG TCTGCCTGGC AGCTGCACCC TCATCTGACA TGCAAGGCGG GGTCAGACAA 960
GATAATCTGA ATATTCCTTC ATCCCCCAAC TTGTGATTTT GTTTCTATGA TTTATACCCA 1020
GCCCAAAGAT GCTATTTCAC AAAATGGGTT TTGTGGCTTG TCTAGACAGG AATACAAGGC 1080
CTCAGGCAGC CACGGAATCA CAATTAGCGA TCCATTCACA CTAGCACCGA ATATTCCCAC 1140
GGAAAGGCCG TGCAGTGATT ATCTCTAAGG ACAAGGACTG TGTGTGAAGA AGGACAAGGA 1200
GAGAGGAGCT CCCGCGACTG CCAGGTCCAA ATGGAATTTT ACATCGGAAA TGACAGCTAC 1260
TTACTAAAGT CTTGTAGCTT 1280