EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-16087 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr18:46458350-46459810 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PHOX2AMA0713.1chr18:46458957-46458968TAATTCAATTA+6.14
Phox2bMA0681.1chr18:46458957-46458968TAATTCAATTA+6.14
ZBTB18MA0698.1chr18:46459295-46459308TTTCCAGATGTTT+6.28
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00297chr18:46453448-46463365Adipose_Nuclei
SE_01041chr18:46459044-46460317Adrenal_Gland
SE_01674chr18:46457621-46461046Aorta
SE_02345chr18:46457751-46460896Astrocytes
SE_02959chr18:46458698-46460174Bladder
SE_03502chr18:46458581-46460377Brain_Angular_Gyrus
SE_04121chr18:46458068-46463294Brain_Anterior_Caudate
SE_05251chr18:46453949-46463370Brain_Cingulate_Gyrus
SE_05955chr18:46446481-46480088Brain_Hippocampus_Middle
SE_07264chr18:46457869-46462563Brain_Hippocampus_Middle_150
SE_08312chr18:46458017-46462377Brain_Inferior_Temporal_Lobe
SE_11810chr18:46458125-46462505CD20
SE_23482chr18:46457659-46460241Colon_Crypt_1
SE_24271chr18:46458440-46458674Colon_Crypt_2
SE_24271chr18:46459179-46460300Colon_Crypt_2
SE_25133chr18:46459371-46460641Colon_Crypt_3
SE_26097chr18:46458359-46459987Duodenum_Smooth_Muscle
SE_26908chr18:46457922-46461057Esophagus
SE_27698chr18:46448262-46462356Fetal_Intestine
SE_28705chr18:46448500-46462248Fetal_Intestine_Large
SE_29974chr18:46458130-46462319Fetal_Muscle
SE_31550chr18:46457709-46461104Gastric
SE_36338chr18:46458673-46462143HMEC
SE_38707chr18:46454005-46462116HUVEC
SE_41124chr18:46457858-46462756Left_Ventricle
SE_42227chr18:46457684-46479968Lung
SE_43780chr18:46453091-46463232MM1S
SE_44360chr18:46458233-46461581NHDF-Ad
SE_45015chr18:46458374-46459652NHLF
SE_45645chr18:46452288-46478469Osteoblasts
SE_46741chr18:46459427-46460824Ovary
SE_47308chr18:46448347-46478259Panc1
SE_48618chr18:46457650-46471726Right_Atrium
SE_50188chr18:46454783-46471671Sigmoid_Colon
SE_51514chr18:46458128-46463379Skeletal_Muscle
SE_52478chr18:46452303-46462338Small_Intestine
SE_53633chr18:46458273-46462345Spleen
SE_55015chr18:46458500-46462318Stomach_Smooth_Muscle
SE_59097chr18:46453600-46480091Ly3
SE_62146chr18:46454581-46479860Toledo
SE_62532chr18:46448756-46483085Tonsil
SE_65410chr18:46457610-46462370Pancreatic_islets
SE_67202chr18:46453091-46463232MM1S
SE_68537chr18:46428073-46479503TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr184645861146458800
chr184645936746459671
Enhancer Sequence
CCCCCCAGCA GGGTTTTGAT TGTGCCCCCA CTGAGCAGGA GATGGGGCCC ATCTATTTGT 60
AAGAACGGTA TGGTGCACTC AGATCACACT GATAACTAAC TTTTTAATTT TCCCTCTTGG 120
TTACTGATTC ATGAGGGGGT GGGGCAGGGC TGGCTCAGAG GCTGCAGTGA GGCTGACAAG 180
GTCCCCAGGC CCAGCTCTTG ATGATCCTCA CTTAGCCTGC AGGGGAAGGA GACACTTAAC 240
AGCTTCATGA GGTGACTGGA AGGTGGGACA GGGGACAGGG ACAATCATTT AACCTCCGAG 300
TGAGCCACCC CAGAAAATGC AGACAGCTAA TCTGCCAACG GCACAGTCAT ATCTTGGCGT 360
CTTATTGTTT TTGTTCCTGT TGAGTGACAG TCGCAGATCA AAACGTAAGA AAGCAATACT 420
GAAATGAGCA CACAGTCGCT GGCCTGGTTA TCTGAGTTGT CTTCTGGCTG AAAGAAAGTC 480
CCGACTTTGC AAGATGAAAT TGGAATTGAG ACCAGATCTT CCCTTTCTGC TCTGATCAAA 540
CCCCCCAGCA AAAGCAGCTC TCCCCGCCTT TTCTTCCTGG TGGGGCTTCA CGGAGGAGCG 600
AGAAGAGTAA TTCAATTAGT GAACTCCACA GAGCTTGGAA GCCATCGGTT GGCCCCGGGG 660
GAACAGACAG AGAAGGATGA ATGTGAAAAG GAAACACCCT GGTAACTGCA TCTTAGATTA 720
TTTCATCCAA ACCCAACCCC AGACAGGCCA GGGCCTCACA CACAGGGCTG ACACCTCAGA 780
AACGGGCTTA ACCCTCAGAT TTAAAATTAA AAAGCAAGAA TTTCCTTCAT CCCCCAGATG 840
GTCTTCGTTG CGAATCAAGT CCTCTGGAGT TACAAAGGGA AAGTCACTCC TGGGCTTTGA 900
AAACATCCCA CTTCTCCTCT GGCTGTCAAG ACATTAGATA CTGTCTTTCC AGATGTTTCC 960
CCACCCCTTG GCCGTGGTCC ACTGAGGAGC CTGGCGCTAG GCTGGTCACT TCCACTCTGT 1020
GCTGTGCCCC AGGTACTACC AGGGTCTGGA GGGTGGATTA TAACCACAGC TCCTGTTCTT 1080
CCTGCTGTCA TCTTACAATC AGCAAGAAGC GGGGTGGGGA GGCGGGCTGG AACCAAAACC 1140
CGGGAGACCT ACCTCTGTTT ATCCACAAGC TTTGCTTTAT CTCAATTCTC AACAGACCAC 1200
ACAACCAAAG CAGAAGTAGA AGTGGATGAC TCAAGAGCTA GGCCCATCCC AGGGGGCCCA 1260
CCCTGCACCT CCCCCACCTA TGGCCTGGCT TCATGGAGGG ACCAGGCTCC TCTGTCCTAC 1320
AGAAGCTGCC CCTGCCTGCC TCCAGGTAGA GGCAACTCCT AGTCAATCCC CCCTCCCGCC 1380
GGCTCCATCC CCATGGATTC AACATCACCT TCGGACAAGC CATTCCAACT GCCAATTCTT 1440
AATTCTAACC CAGCCCAGGA 1460