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

TagContent
EnhancerAtlas ID
HS059-23713 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr19:47600150-47601080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17716478chr1947600593hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MafbMA0117.2chr19:47600582-47600594AAACTGCTGACG+6.02
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_03022chr19:47598055-47600395Bladder
SE_04522chr19:47597859-47601876Brain_Anterior_Caudate
SE_06463chr19:47596498-47603370Brain_Hippocampus_Middle
SE_07150chr19:47598244-47601908Brain_Hippocampus_Middle_150
SE_08585chr19:47597109-47601648Brain_Inferior_Temporal_Lobe
SE_11185chr19:47596089-47600251CD20
SE_13373chr19:47600379-47601265CD34_Primary_RO01536
SE_17540chr19:47596774-47600508CD4p_CD25-_CD45RAp_Naive
SE_17955chr19:47596306-47600458CD4p_CD25-_CD45ROp_Memory
SE_23136chr19:47596536-47601740Colon_Crypt_1
SE_23866chr19:47597093-47601786Colon_Crypt_2
SE_24862chr19:47596917-47601736Colon_Crypt_3
SE_25954chr19:47596517-47601744Duodenum_Smooth_Muscle
SE_26646chr19:47596502-47602696Esophagus
SE_27626chr19:47596238-47604236Fetal_Intestine
SE_28544chr19:47596123-47604268Fetal_Intestine_Large
SE_31552chr19:47596626-47601943Gastric
SE_34095chr19:47597597-47601630HCC1954
SE_36699chr19:47598365-47600618HMEC
SE_41315chr19:47598005-47601805Left_Ventricle
SE_42396chr19:47596544-47602441Lung
SE_47643chr19:47597827-47600486Pancreas
SE_47643chr19:47600602-47600920Pancreas
SE_48411chr19:47596498-47602335Psoas_Muscle
SE_49033chr19:47598058-47600543Right_Atrium
SE_49033chr19:47600551-47601779Right_Atrium
SE_50229chr19:47596382-47603151Sigmoid_Colon
SE_51583chr19:47596585-47601903Skeletal_Muscle
SE_52381chr19:47596493-47602514Small_Intestine
SE_56677chr19:47600272-47601347u87
SE_57563chr19:47599728-47600528VACO_503
SE_58017chr19:47599738-47600436VACO_9m
SE_62357chr19:47596302-47618092Tonsil
SE_65381chr19:47596646-47601723Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194760039047600645
Number: 1             
IDChromosomeStartEnd
GH19I047093chr194759643347604071
Enhancer Sequence
TCAGCACGCC CTCCCTTATG TCCAACACCG CGGCACAGCA GGCGACAGTC TTGCCCAGGG 60
TCAGCTGAGG CCTCCTTCCC TGTCCTGATG CCACTCGCTG GCTCGGACGA AGGTACAGGC 120
TACTCTACAT CTAACACCTG CGGGCAGAGG ACAAAAGACC ATTCAAGGAA CTCCAAGAGC 180
CTTAACCATC ATCCAGAATG ATTCTAGAAA GGAATCACCA AGGTAGAGAA GTGCAGCATT 240
CAAATTCACC CTACAAAGAC CTGAGCCAAA GAGGGATTCT GCACATTATC GATATTAACA 300
GCTCCAGGCA CATCTGGGCT CAAAGAGAAT CAACCATACA ACTTTTCACA AAACAGGCAG 360
TGACTACTTG AAATTTTGTT TCCCTAAAGT TGAGAGAGGC AGAGAAATAC ATAGGATTTT 420
TTTGTTGTTG TTAAACTGCT GACGGTTGAT AAAGGGGCAC TGAGACAGCA ACAATAAACA 480
GATCACTGCA TTCTCAGGGC CCTCTGGCCA TGTCAGGCCC TCAAGCCCCT CCGAGCCCTG 540
GGCTAACTTC TGTCCACAGT CACCTCAAGG GGTCCCCCCT CACGACACCC AAGATGCTCT 600
CCTAGCTAAA CGTCCTGCGT GAACACGAGG TCTTGACTAT ATTCTTCAGA CTCTGTTCAA 660
CAGAAAGCAA AAAGAAAGGA AGTCGAGCCA AATGGGAATC CCGTGGGCCA CCAGCGCGAC 720
GGCACAAAGG CGGTCTCAAC AAAACAGCAA CCAGGTTTCA GCGATGCCAC TTAACAGACT 780
GCCGGCAAAA TCCGTGTCAG AGTGGGATTA AATGCCAAGG GAACATGCTT AATAGACCTC 840
GACATAATCC CCCAAGAAAA GTGGGGGAAG CCCCACCGCG CTAATCATTT CAATCTAGAC 900
CTGCCAAACT CTCTTGAGAC AAGCAAGCAG 930