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

TagContent
EnhancerAtlas ID
HS095-12886 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr17:49007870-49009410 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr17:49007882-49007903CTTTTCTTTTTCTTTTTCTTT+6.02
IRF1MA0050.2chr17:49007888-49007909TTTTTCTTTTTCTTTTTTTTT+6.09
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00952chr17:49008090-49009458Adrenal_Gland
SE_02991chr17:49008216-49009426Bladder
SE_03517chr17:49008133-49010338Brain_Angular_Gyrus
SE_04178chr17:49007034-49010780Brain_Anterior_Caudate
SE_05235chr17:49005795-49010989Brain_Cingulate_Gyrus
SE_06067chr17:49006595-49011079Brain_Hippocampus_Middle
SE_07466chr17:49006815-49010823Brain_Hippocampus_Middle_150
SE_08267chr17:49005967-49010872Brain_Inferior_Temporal_Lobe
SE_08899chr17:49008165-49008460Brain_Mid_Frontal_Lobe
SE_08899chr17:49008640-49009319Brain_Mid_Frontal_Lobe
SE_12167chr17:49008111-49008989CD3
SE_19619chr17:49008215-49009447CD4p_CD25-_Il17p_PMAstim_Th17
SE_23191chr17:49008216-49009312Colon_Crypt_1
SE_23784chr17:49008246-49009341Colon_Crypt_2
SE_24830chr17:49008286-49009488Colon_Crypt_3
SE_26011chr17:49007719-49010219Duodenum_Smooth_Muscle
SE_26691chr17:49008101-49010781Esophagus
SE_27621chr17:49008042-49009688Fetal_Intestine
SE_28540chr17:49007777-49009732Fetal_Intestine_Large
SE_29967chr17:49008050-49010147Fetal_Muscle
SE_31399chr17:49006975-49009500Gastric
SE_35088chr17:49007818-49013922HeLa
SE_37666chr17:49007709-49010284HSMMtube
SE_41117chr17:49008026-49010839Left_Ventricle
SE_42844chr17:49007916-49010813Lung
SE_47468chr17:49008217-49009396Pancreas
SE_48151chr17:49007182-49013769Psoas_Muscle
SE_49193chr17:49008011-49009448Right_Atrium
SE_49713chr17:49008186-49009313Right_Ventricle
SE_50311chr17:49008119-49009392Sigmoid_Colon
SE_51156chr17:49006841-49011214Skeletal_Muscle
SE_52502chr17:49008091-49009506Small_Intestine
SE_54412chr17:49008018-49010190Spleen
SE_54634chr17:49004692-49010870Stomach_Smooth_Muscle
SE_57199chr17:49008277-49009339VACO_400
SE_59738chr17:48979175-49044314Ly4
SE_65373chr17:49007639-49010495Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174900820049008564
Number: 1             
IDChromosomeStartEnd
GH17I050930chr174900793349013741
Enhancer Sequence
ACGTCCCCCA GCCTTTTCTT TTTCTTTTTC TTTTTTTTTT TTTGAGATGG AGTCTCACTC 60
TGTCCCCAGG CTGGAGTGAA GTGGCACAAT CACGGCTCAC TGCAACCTCT GCCTCCCGGG 120
TTCAAGCGAT TCTCCTGCCT CAGCCTCCAG AGTAGCTGCG ATTACAGGCA TTCGCCACCA 180
CGCCTGGCTG ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CGCCATATTG GCCAGGCTGG 240
TCTCGAACTC CTGAGCTCAG GTGATCTGCC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC 300
AGGCGTGAGC CACCGCTCCC AGCCTTTTAA AAAAGATGCT CTATAATTTG AGATGGTATG 360
GTTGCTGCAA AGTTTATGAG ACTATTCTCC ACATTGTCAA ATATTTTGGT AACTTCCAAT 420
TTTAGTTATT TTATACAATC TTGCAAAGGG CCGTGTTCAG CGCTCCACGG AATTGCAGGG 480
CTGGGGGACA CTCCATTCCT GCGTCCTAGA GAGCCTCTTT CAAGCAAGCT CTTTCAAGCA 540
AGCAAGGAGT GCAAATCCTC CTGCCTGCAA ATTGCGGGCT GTGAGGCCTG AGCCAACGCA 600
CTGGAGCTCT CTGAGAACGG CTGTGACGAG CCGAGCTAAC AATAGCCCTG CTTAGCAGCC 660
CCGCGGCGGC TGACTTGGTG AGGCCCGCAG GCCCGCCTCA GCCCGCCCTC CCTCCGCCGT 720
CCGGGCAGGA GGTGCAGGGG CAGCAGGGCC CGCCTGGCTC GCTGCGGCCG CTTATCAGAG 780
CCGGCTGTGG CGCCGGTTAC GTAACCGGGC GGCTAATGCT GTTTTACTTG TCGATGAAAC 840
CCAAATTAAA AGAGGAAATT ATTGTCCTGA TGCTCAACTC GCCTAATCCC CATCTGTCTC 900
CTCTCTGGTC CCCCGCGCTG CCGAGCGCTC GCATCTAAAG GTCTTGAACG CGTTCCAGGT 960
TTCTAATTTC GTTTGCTTAT GCAACCAAAA ATATTATGGC CGCGTTTCCT GGGGGTGATG 1020
AAGTCTATAT TCTGGGCTAC AGGCACACTA AAAACGGCAG CGCCAGGGCC CAGCGCCGCT 1080
CGCGCGTGCA CCACGCGCCG GCTTTTTTTG GTTCCTCCGA GGCGCGGGCA GCTCTGCAGC 1140
CGCGGGGGCC GCAGGAGGTG GGGGCTGGAC CCGCCCGGAG CTCGGGAGGG CCCGGGATGG 1200
CCCCGGGGAG CGCAGGTCCC GGCAGGGGCC GAGCGAACAA GGGCCGGCCT GGGGCGCCCA 1260
GAGACGCGGG GGACCGTTCT GGTCGCAGCT GCCTGGGTGA CCTCTTGGAA CCTCAGCTTC 1320
CTCCTTGTTT TTTTTCTGAT TCTGACTCTG ATTCCTGTGT GCTGAATCCA GGCTGTAGTG 1380
AGCTGTGATC ACACCACTAC ATTCCAGCCT GGGTGGCAAA AGGAAGATGA GAGAGAGACA 1440
GAGAGAGAGA GAGAGAGAGA GAGAGAGAGA GAGAGAAGAG AGAGAAATAA GGGAGACATC 1500
AACACCCTGG AATATTGTGT AGATGAGTTT TAAAAAAAAA 1540