EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-10590 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr18:74813250-74814980 
Target genes
Number: 1             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr18:74814940-74814951AATGAGTCACC-6.02
FOSL2MA0478.1chr18:74814941-74814952ATGAGTCACCC-6.14
JUN(var.2)MA0489.1chr18:74814941-74814955ATGAGTCACCCTCC-6
JUNBMA0490.1chr18:74814941-74814952ATGAGTCACCC-6.32
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_02611chr18:74812597-74816746Astrocytes
SE_09139chr18:74806175-74829571CD14
SE_11015chr18:74809799-74821940CD20
SE_12122chr18:74812595-74815611CD3
SE_12973chr18:74813210-74815301CD34_Primary_RO01480
SE_13574chr18:74812846-74815418CD34_Primary_RO01536
SE_14365chr18:74812674-74816280CD34_Primary_RO01549
SE_15148chr18:74810251-74821398CD4_Memory_Primary_7pool
SE_16599chr18:74811009-74815164CD4_Naive_Primary_8pool
SE_17992chr18:74810218-74822100CD4p_CD25-_CD45ROp_Memory
SE_18533chr18:74809958-74822708CD4p_CD25-_Il17-_PMAstim_Th
SE_19370chr18:74810542-74821336CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74797810-74821764CD56
SE_22307chr18:74808493-74829791CD8_primiary
SE_25341chr18:74808379-74829893DND41
SE_25885chr18:74812426-74817816Duodenum_Smooth_Muscle
SE_26884chr18:74812156-74814621Esophagus
SE_30168chr18:74812665-74817389Fetal_Muscle
SE_31917chr18:74812700-74814544Gastric
SE_32648chr18:74811022-74816167GM12878
SE_36043chr18:74811917-74816801HMEC
SE_37921chr18:74812593-74816544HSMMtube
SE_39287chr18:74812583-74816766IMR90
SE_39556chr18:74812667-74815384Jurkat
SE_41189chr18:74812826-74814910Left_Ventricle
SE_42218chr18:74812647-74814668Lung
SE_44218chr18:74812664-74817054NHDF-Ad
SE_47137chr18:74808444-74829846Panc1
SE_48227chr18:74812721-74814680Psoas_Muscle
SE_49182chr18:74812714-74814536Right_Atrium
SE_50555chr18:74812624-74814502Sigmoid_Colon
SE_51089chr18:74812396-74822600Skeletal_Muscle
SE_52417chr18:74811440-74814767Small_Intestine
SE_53332chr18:74808902-74814723Spleen
SE_58547chr18:74756065-74865317Ly1
SE_62520chr18:74808577-74846347Tonsil
SE_64359chr18:74812447-74816186NHEK
SE_65574chr18:74812584-74814367Pancreatic_islets
SE_66494chr18:74812667-74815384Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr187481327274814146
chr187481336174814191
chr187481433574814742
Number: 1             
IDChromosomeStartEnd
GH18I077094chr187480680074829611
Enhancer Sequence
ACAAAATGGG CAGAGTGATA GAAAGCTGGT AAATTAGTGA GGCAGGACCA TTTGGAAACC 60
AAATTTCCCT GCAACTTAAA AAACACAGGG AGTCAAAGGC AGAACAGGAG TTTCTTCGTT 120
TCTGAGAAGG AGCGCTGTGC CCTGAACCTG CGCCTGCCTG GAGGAAGTTA CACTCCATCC 180
GCATGAGTGA ATCATGAGTC AGGAGGGCAG GCTGCCCACT CCTCTGATGG GCGGAGTGCT 240
TCTGCCTGAA TCTGATGTCT CCTGTTCTGA CCCTCAACTG GCCCAGGAAG GTGGCTCAAC 300
CACTTGTTAC CAGGGACCTG CACCCCATAT GAGTGGACTA ACACTGCAAC TCCAGAAAAG 360
TGTCTTTTTT TCACCAATCA GAGACATTCC ACAGTTAACC CTTTAGTTAG TTTCTCTTCC 420
TCTTACATCC TGCCGTGGCT TATTCGGGAT GAGAGAGAAG CAAATTTCAA AGCCCTGAGT 480
CACTGAGGGC AAAACTTGCA AAGGAGACTG GAAGCTCCTG CAGGCAACAG ACGAGGCCTC 540
CCCACCACCT CCCCAGCAGC CAACGGCACC TAAAGCCTGC TCAGGAAACT GAGCTTTTAT 600
GTGAAAAAGA AGTTAGGAAA TAGGTATGAT TCATTTACTC TTTCGAACAT CTGTAAGCCA 660
GTTATGTGCT GGGGATGCTC CAGGCTTAGA GACGGAGGCA TCAGAGAGAG GAAAGTTCCC 720
TCCTTGATAT AGGAGGGGAA GAAGTCGGAT GATAAACAAA TCACCAGGAT CTGTATCAGA 780
GCACTCAGCC GCAGGCTCTA TGACAGCAGA GGAAAGAATC ATCTAGTGTG GGTGGGGAGA 840
GGTGGAGAAG GTGGCAGCAG GGTGGGAAGG AGGGGGCCCT CAGCAGCCTG GGCCGGGCAG 900
TGGGGCAGAG GCAGTGTGTG GGGTAGACCG GGCAGCCCCC ACCGCAGCTG CCCTCCCTGC 960
TGACAGATCA GTAACCAGCA CCTGAAACTG ACAGAAACTT TCCTTGACTC TCTCATAAGG 1020
GGGAAAAATG CCTCCCAGAA TCACACACAG AAATGTGCAG AGTGGTAGGT GACACGGCTG 1080
GAGCTCATGT CACGTTTTCT TTTGTGATTC AAGTTTAATG CTCTACTAAG CTATGCAGCA 1140
TCACAGAACA TGTACATGTA CTTGGAAGGG CACAAAATAT TTCCCATCAA GTTTAAAGGA 1200
AAGAAAAAAA AGCTCTTACT TCTTAAAACT ACCTACAGGA ACCATAGTTT TAACATTTCC 1260
AAGTTTTGAG GTTTTTAAAT GATCAGAACT TTAAACATGA GATTTCAGAA AACAAAAGCC 1320
TCAGCATGGG CTTTGCTATG GCTCAAAATC TTACTCTGAT AGCATTAAAC AAATTAAAAA 1380
CATATGTGGG TGTTTTACAG CGTCAAACAA CAGGAAAGAA ACTGTACACC ACAGAGAGGT 1440
TTCTTGAAAC TGGAGTTGCA AATCAGTCAT TCTAAGACTT AAAATACCAA CAGTGTTAAC 1500
AGCCTAGAGG CCTCTGAGCA GAGCTGTTTT TTCCACTTTC ACTTTAGGTG AAACTTAATC 1560
CTCCTGGTGC AGATACTGTA TCCAAGCCAT GTTCTTAATA AATTAGTAAC TTAATACATT 1620
TATGGTTGTT ATTGCTAATT ATAATGCTGA CATTATCAGT AATACAGTTT AAGTATGGGC 1680
TGAACAAAAT AATGAGTCAC CCTCCCATTC AACATTGACT AGAACCATTT 1730