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

TagContent
EnhancerAtlas ID
HS010-01491 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr14:77422120-77423330 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr14:77423113-77423128CTGCTGACTCAGCAC+7.55
MAFFMA0495.3chr14:77423113-77423128CTGCTGACTCAGCAC-7.61
MAFGMA0659.1chr14:77423110-77423131CCGCTGCTGACTCAGCACTTC+6.16
MAFGMA0659.1chr14:77423110-77423131CCGCTGCTGACTCAGCACTTC-6.47
MAFKMA0496.2chr14:77423111-77423130CGCTGCTGACTCAGCACTT+6.78
MAFKMA0496.2chr14:77423111-77423130CGCTGCTGACTCAGCACTT-7.17
ZNF263MA0528.1chr14:77422786-77422807ACCCCCTCCTCTTGCTCCCCT-6.14
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_01254chr14:77420883-77424353Adrenal_Gland
SE_08284chr14:77420765-77424468Brain_Inferior_Temporal_Lobe
SE_24529chr14:77422128-77423800Colon_Crypt_2
SE_27091chr14:77419455-77426235Esophagus
SE_29618chr14:77420671-77424362Fetal_Muscle
SE_31928chr14:77421729-77426154Gastric
SE_32994chr14:77421752-77424066H1
SE_33446chr14:77420480-77424488H2171
SE_34422chr14:77418557-77429646HCT-116
SE_34742chr14:77415823-77429622HeLa
SE_37233chr14:77415973-77429404HSMMtube
SE_38430chr14:77419198-77429214HUVEC
SE_41258chr14:77419224-77429300Left_Ventricle
SE_41987chr14:77421767-77424998LNCaP
SE_42676chr14:77420714-77426260Lung
SE_44184chr14:77419413-77424284NHDF-Ad
SE_46080chr14:77419415-77424550Osteoblasts
SE_46723chr14:77422105-77423789Ovary
SE_47949chr14:77422035-77423590Pancreas
SE_48706chr14:77421709-77426250Right_Atrium
SE_49653chr14:77421766-77424358Right_Ventricle
SE_50880chr14:77420706-77424364Sigmoid_Colon
SE_53991chr14:77419420-77424483Spleen
SE_55769chr14:77419401-77424613u87
SE_65382chr14:77419164-77426315Pancreatic_islets
SE_67544chr14:77419401-77424613u87
SE_68739chr14:77421020-77425262H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr147742224077422571
Enhancer Sequence
AACAAAAAAG GTAAAATCAG AGGGTGGTAA AAGCTATGAA GGAAATAAAG CAGTATAACT 60
GCTTAAGGAG CAGGGACCTC TGCAGGTGGA TGGCAAGGGA AGGTCTCTCT GCAGAGACGA 120
CATTGACATT CATGCTGAGA CCTGGGCCAG CCATGCAAAG AAGGGGGGTG TAGGCAGAAG 180
TGCCGCAGTG GGAACAGGCT AGAAGTTGGG CCTGGTGCTG GGACAGTCCC AGTTCAGGCA 240
TGTCCTCCTG GTGTCGTTTT TAATAGCTCA TCCTTTCACA ATCAAGAGTG GCTCATGCCG 300
GAGATGAGTT ACCCGCAATG AGGGGCTGGA TTTATTCTAA GGGCAGAGGG AAGCCATCAC 360
AGGAAATGAT GTGATTGATG TTTTGAAAAG AACTCGCTGG CTGTTCCGTG AAGAATAAAT 420
TAGAGGGGCA GGAGGGAAGA AGTCTGCCTG GGGCGGCTGC AGCAACCCAG GCGTGCTGCG 480
AGGTGCCCTT TGACTAGATT CCAGTGGGGG CTTTCGGGCG AGCAGAAGAA CCCCAGGGAT 540
CAGCTCTAGC CACGCTCAGC TCCCTGGGCC GGCCCTGGGC ATTTCTGAGA CGGCCCTCGC 600
GCTCAGGGAC CTCTCCTCGC AGTTCCATTG TCTGTTCTTG CGGAGTCCTG CCACACTGGG 660
AGGGCCACCC CCTCCTCTTG CTCCCCTCCC CTCCCCGGGT CCAGCCCCTC CCCTGCCTGG 720
CCCGGCTGCC GCCCAGCGCC AGCCAGAGCC CACCCCGCCT CCCTGCAGGA AGCCGGCTGG 780
CGGCGCCTGC TGCGTGACCT TGGGCTGCAA AGTCGGGCGT TTGCAAAGTC AAAGCGAGTC 840
ACTTCCTCCC CCAGGCCTCC CCCGAGCGGG CAGCCGGCCG CCGCTCCCTG CCCCCTCGCC 900
CGCCGCGGGC CGGGGCTGGC GCTGGCACGA ACGCGCTCTG CATGCTAAGT GCTCGCGCCC 960
GTTCCCGCCG CCCGGAGGCT CATTTGTCAC CCGCTGCTGA CTCAGCACTT CTGCAGAAGG 1020
CTTTTCCCTC CGCTTTGGAG GAGGAGGCCC GGAAATGAGG CAGAGGCTCT TCCTTCCCTT 1080
CCCTCCAGCA GGGGTGTGTG GCGTGGGTGT GTGCGGGTGT GGCAGGGTCT GTCTGTATGT 1140
CTGATGCCTG TCCATCACCG GTGTATATTT TCGCGGCTGT GTCTGTCTTT TGTGTATGGC 1200
TGAGTCTGTG 1210