EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS081-00113 
Organism
Homo sapiens 
Tissue/cell
HACAT 
Coordinate
chr1:16469710-16472580 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:16470593-16470611GCCTCCTTCCTTCCGTTC-6.21
EWSR1-FLI1MA0149.1chr1:16470589-16470607CCTCGCCTCCTTCCTTCC-6.66
Nr2f6(var.2)MA0728.1chr1:16470183-16470198GAGGTCAAGAGGTCA+8.55
RARAMA0729.1chr1:16470183-16470201GAGGTCAAGAGGTCATGG+7.96
ZNF263MA0528.1chr1:16470585-16470606TTTCCCTCGCCTCCTTCCTTC-6.04
ZNF263MA0528.1chr1:16470632-16470653GAGGGAGAGAGGGAGGGAGGG+6.8
Znf423MA0116.1chr1:16470744-16470759GCCACCATGGGGGGC-6.1
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01311chr1:16469763-16474276Adrenal_Gland
SE_23091chr1:16469542-16473316Colon_Crypt_1
SE_23751chr1:16469661-16472353Colon_Crypt_2
SE_24743chr1:16469690-16472751Colon_Crypt_3
SE_26540chr1:16467219-16474484Esophagus
SE_28102chr1:16469515-16474402Fetal_Intestine
SE_29455chr1:16469509-16474264Fetal_Intestine_Large
SE_30715chr1:16470911-16474428Fetal_Muscle
SE_31527chr1:16467241-16474177Gastric
SE_34268chr1:16469534-16484371HCT-116
SE_34628chr1:16464389-16475128HeLa
SE_35569chr1:16469536-16474542HepG2
SE_36144chr1:16469776-16474435HMEC
SE_38062chr1:16469618-16476064HUVEC
SE_39172chr1:16470299-16474345IMR90
SE_40833chr1:16464800-16474529Left_Ventricle
SE_42443chr1:16464217-16474534Lung
SE_44998chr1:16470436-16474414NHLF
SE_46140chr1:16470271-16474690Osteoblasts
SE_47150chr1:16463762-16486412Panc1
SE_47539chr1:16469712-16474272Pancreas
SE_48744chr1:16464918-16474528Right_Atrium
SE_50427chr1:16469493-16474380Sigmoid_Colon
SE_52536chr1:16469494-16474248Small_Intestine
SE_53900chr1:16470095-16474531Spleen
SE_56795chr1:16467226-16474542VACO_400
SE_57357chr1:16469076-16474106VACO_503
SE_57939chr1:16469612-16470513VACO_9m
SE_57939chr1:16470606-16474158VACO_9m
SE_64726chr1:16469669-16473818NHEK
SE_65472chr1:16469318-16473765Pancreatic_islets
SE_69141chr1:16469773-16474224H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11646988816471234
Enhancer Sequence
ATGGGTGGAG GGGTGGATGG ATGGATGAGT GGATGGGTGG ACAGGTGGAT GGAAGAGTGA 60
GTGGGAGAGA GAATGGGTGG CAAACCTACC ATGTGCATGT GAAATATGCA CTCCAGGGCC 120
AGAGAAATGA GCAGTGTTTC AGCGCCCAGA GAGACACTGT GGAGAAGGTC CACCAGGATG 180
CCTACCTGCC TTACACAAGA GCCTAACTTT GGCACACCTG TGGCACACCT GTGGAGAGCT 240
GTTCTGGCCC CGGTTGTCTG GCAGGCCTGG GCTACTCCGA GCAGGGGAAC TGGGGCACAG 300
TGGCTGCACC TCCGGCTATA CCCTGGTTTT TCCAGTTCCT GATGCCCGCC CCTCAGGTGG 360
CAGCATGAGG TGACTCAGGG ACAGACGCCC TTATCGTGAC GCAAGTCCAG CCCCCAGTGG 420
AGCCCCTCCT CCCAAGGCAC AGCCACCTCC CAGGCTGGCA ATGGCAAGGT TGTGAGGTCA 480
AGAGGTCATG GTGGCAATTC ACCTAGGGCC AGTCACCGCC CAAGCCAGGC CCAGCAGGTG 540
ACCGCAGGAA CCACCTTGGC CCAGGGATGT GGAGCTTGGA CTTTGTCTCT GGGCCCTGAC 600
AGACGGCAAA TGGCGACCTA TGGGTTACTG ACCCAGCAAA TGAGGGAGCT GACAACCTCA 660
GGCCCTGGTG GCTTCTTGCT CCCAGCAGGC CCTGTCGTCT CTGCAGAAGG GGGGCTGCCC 720
CCAGGGCCTG ACGGCTGCCA GCACCCTGTC CCTTTCACAC ACACCCTAGG GAGCTATCTG 780
CAGGCACATT CCTCCACCAT TGATAAGCAC CACTCCCCAC CTCAGCCCCC GCCTACCGCT 840
CCTGTCCTGC CTCCAGCCTT TCATCTTCTG TTTGCTTTCC CTCGCCTCCT TCCTTCCGTT 900
CTGGGGACCC ACTTACCTCC AGGAGGGAGA GAGGGAGGGA GGGAGAAGCC GGTGCCCGCC 960
CAGCGGAGAT GCCAGCGCCT AGCTTTGCCC CCAGTGTGAG CTGAGGGTGG GGCAGACAGG 1020
GCACAGAGGT GAGAGCCACC ATGGGGGGCT GGGGGTGCTG CCACCGTGGT CCCACCTCTG 1080
TAGGCCAGAA GAAACATCAC AGAAATAAGG CCTGGTGGGA CTTCCCAGCA GGGGACAAAG 1140
CCTGCGAGCC ACAGCCAGCA GCTCCCAGAG TCTTCCACCT GGGGGACCAA CTGTGATCTG 1200
ATGAAACAGG AATCCTGCCA GCAGCCCCTG CCATGGCCCG AGACCACCCT GTCTAAAGAC 1260
CACCTTAACC ACAGACATAC CCTGGCCAGG GGACTCCTCC CTGTCAGCTA TGGACTTTAG 1320
GCCACTGGGG CTGTAAGCAG TGGGACCCCT CCTCACCACA CTTGTGTCAC ACAGTCAACA 1380
GCTTCCCCGG TGTTCAGACT GAGCCCCAGT GGGAAACCAC AGGAGGGAAG CTCGGATCAC 1440
CAGGTTGACA GCGTCCTTCA GGGCCACAGG TCCAGCCCAC TCATTTTACA GATGGGGGTG 1500
GGACCCCAAG GGGACCTGCT AAGGTCATAC AGCCTGTGGG TGGAAGGACA CACACCAGGG 1560
GCAACTGCCT TCCTGTGCCA GGCCCCCGTT CTTTTGGTCA CTGTTCACTG CTTCCTCTCC 1620
GGACCTCAGT TTCCTCATCT GTAAAATGGG GATCAAGTCC TCATCCTCTC TGGGTTGTGT 1680
GTGAAGATGG AAGAAAGCCC TGCTTATGAG ATGTCCAGCA TGGTGCCTGG AATGCGGTGT 1740
CCCTATGAAC TAGGGGATCA TGAAACTACA GTAGGGAGGG GACCTCCCCA AGGGGCTGGG 1800
CCCCTTGAGG GAGCAGGAGC CTCTCAGGAG GGAATCTCCA ACTCCCCACA ACCCCAGCTC 1860
TGGCCTCCCA GCTGTTCAGC TGAGCCACTG GCCAAGGCTG CTGGCCACCT GCTCACCTGA 1920
CCAGCGGTCC CCAGGGCTGA GGCGCCAGCA GGGGCCCCGC CAGCTGCTGA GGCCAGCACA 1980
GGAAGCGGAG ACATGGAGAC AAAGCAGCCC CCGGGGGACA GCGGTCAGCC CGAGCGACTC 2040
CACTGTCCCC GCAGGCAGGG CCGGGGGCAG GGCGGGGGAA CCAAGGGAAG CTGGCTCATT 2100
CCTGACATAG TTCATGGGAG CGCTCCGGGC AGCGTGCCCA CCTGCCGCAC ACAGCACCTG 2160
GGAGGTGCCT CCCTTCCTCT GCCCACTTAA CTCTTTCCTG AGCTCTGGGC TTCCTGGGGA 2220
AAGAACCCTG AGGAGAAACG GACAAACTGG GAATAACCTA GACAAGGTGC CAGGTGACCT 2280
CAGGGTGCCC CGCCTCGCTC TGGGTCTGGT TTGTCACCAG CAGGAGCCCC AGTGAAAGAA 2340
TCTGGGTCTC CAGGCCTGGG GAGGGTCCGG CAGGGAGGGC AGACCCTGTG CCTCCCTCTG 2400
GTTCTCCCTC AATGTACCCA GCAGTGCCCT CTCCAGGACC CCTGCCTCCA ACAGAGCCCC 2460
CAAGCCCCTG CAACAGACCC TGCCATCCCC AGGGCTGGCC AGAGAGCCTA CCCCAGGGCC 2520
AGGAGCTGAG TCAGGGATTC CAAAGGAACT GGTCACTTCC CGCCCCATTT CCTGACCCAT 2580
CCTGCAGCCT GGGCGCCGCT GCACCGCCTG GATTCAGATC CTGATGCAGC CACATCCTAG 2640
CTGTGTGACT TCAGGCAAGC CTCTTTAGCT CTCTGAACCT CAGTTTCCTG GTCTATCAAA 2700
TGGGATTGAT CACAGTCCCT GCCACGCAGA AAGGCGGTGT GGATTCCGCT CGCATGTCTG 2760
ATAAAGCGCT TGCTTGGCTC AGCGCCTGCC CCTCGGACGA CACCCGTCTA CGGTAGCGAC 2820
TGTCATCACT TCCAGCAGCA GCATGGCCAG GGGCTGCTGA GAGAAGTCTA 2870