EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-04439 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr7:44672990-44675640 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GLI2MA0734.2chr7:44675092-44675107CTACGTGGGTGGGCT-6.93
HNF4GMA0484.1chr7:44674404-44674419AGGGTCCAGAGTCCA+6.09
Klf1MA0493.1chr7:44674996-44675007TGGGTGTGGCT-6.14
NFIAMA0670.1chr7:44673611-44673621ACTTGGCACC-6.02
POU4F2MA0683.1chr7:44673340-44673356TTGCATAATTATTGAG+6.32
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_09293chr7:44668114-44680616CD14
SE_12002chr7:44669441-44675480CD3
SE_14587chr7:44668357-44680825CD4_Memory_Primary_7pool
SE_15490chr7:44672497-44675949CD4_Memory_Primary_8pool
SE_16434chr7:44672525-44680593CD4_Naive_Primary_8pool
SE_16951chr7:44669426-44675446CD4p_CD225int_CD127p_Tmem
SE_17851chr7:44668129-44680829CD4p_CD25-_CD45ROp_Memory
SE_18656chr7:44670100-44680815CD4p_CD25-_Il17-_PMAstim_Th
SE_19294chr7:44669461-44675423CD4p_CD25-_Il17p_PMAstim_Th17
SE_20655chr7:44668188-44680617CD56
SE_21218chr7:44672481-44680578CD8_Memory_7pool
SE_22840chr7:44672479-44680608CD8_primiary
SE_24636chr7:44672874-44674105Colon_Crypt_2
SE_24636chr7:44674149-44675329Colon_Crypt_2
SE_26120chr7:44672338-44680827Duodenum_Smooth_Muscle
SE_27427chr7:44672693-44675348Esophagus
SE_27654chr7:44668239-44680825Fetal_Intestine
SE_28557chr7:44668586-44680821Fetal_Intestine_Large
SE_32407chr7:44672719-44680093Gastric
SE_34691chr7:44670606-44681894HeLa
SE_36719chr7:44672712-44674454HMEC
SE_37328chr7:44672508-44680850HSMMtube
SE_40682chr7:44672552-44680631Left_Ventricle
SE_42075chr7:44672899-44675402LNCaP
SE_42544chr7:44672671-44680682Lung
SE_43768chr7:44668130-44675212MM1S
SE_46384chr7:44672195-44675458Osteoblasts
SE_48519chr7:44672671-44680588Psoas_Muscle
SE_49693chr7:44672888-44674157Right_Ventricle
SE_49693chr7:44674163-44674856Right_Ventricle
SE_49693chr7:44674881-44675350Right_Ventricle
SE_50531chr7:44672686-44677149Sigmoid_Colon
SE_52560chr7:44672691-44680563Small_Intestine
SE_53907chr7:44672618-44680662Spleen
SE_62947chr7:44653723-44680812Tonsil
SE_64825chr7:44672758-44674454NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr74467494144675231
Number: 1             
IDChromosomeStartEnd
GH07I044628chr74466800844681598
Enhancer Sequence
TTGTAAGTCA GAGGCAGGCT CAGCTTCCCC GCACAGTCTG AAGCTGGGTG GCGGTGAGAA 60
ATTACTAAAA GGTTAGTGCC GGTTTTTTAG ATGAAGTCAT CATGTTATTA AAAAATAGTC 120
TGTTTAGTCT CTAGGTTACT GTTCTCTGGC TCCCCTCCCC ATCCAAGACT CCCTTGGAGG 180
GAGGTTTGAG GACTTTGGGA TTCTCATATC TCTTCGCGTC CATGATTGGA TCGTGAGGTG 240
AGGAGATAGC CTTTAGAACC CTCTCTTTGA GTGGTCAGTC ACGTGGTATT CCCTCTGAAA 300
CCCTGGAGCA GATGCTTTGT GTAGCTGGGC TGGGGTTCCC CCAAATAGGG TTGCATAATT 360
ATTGAGGACA GATGAGGCCT CAACCAGACG ACCACAGGTG ACCCCAGACT GTGGGTCTTC 420
CTCACCTCCT TGAGAGTTGC AATTCTGAGA GCTGATAAAA TGTGCCATTG TGTGCAGATC 480
TGGGTAGTTT GAAGCGTTCT CATTTCCTGA GGTGTGTCAG AAAGACTGCG TGAGAAAGGG 540
GTCACAGTAT CTTGGATGTC ATCTTTTCAT GCAGTAAAAA GTCTGGTTTC CATGAATGTT 600
TGTATAACAA ACCACCTCAA AACTTGGCAC CAGTGTAGCA TGTCTCATGA CTCTGTGGGT 660
TGGCTAGGTT TCCCCACTCC TCCCACTGCC AGCTCCCTTG GAGCTGAGGC TCACACCAGG 720
CTAGAAGCCA TGAAGGCCTC TGATGTGTCT GGCAGTTTGT GCTGGCTGTT CACTGGGCCC 780
TGCCATCCTC CAGTAGGCCG GAGCGATTCC TGCACAAAGT CCCAGAGTAG CTCCAGACAG 840
GGAAAAGAAA GGCTGTGGGG CCTTTGAGGC CTAGGTCCAG ACCGTACACT GCTACTCCCC 900
ACGCCATTAC CTTGGTTAGA GCAAGTCACA GACAACCCTT AGGGACATCC GTTTGGGGAG 960
AGGAAAAGGC ATGGCCACTG GACAGCCCTC CACAGCTCTT TTCATAATGA CCTGATAGAG 1020
CAGCCACCTT TAGTCTAGTG CAGAATCCCA GCAAATATCA TTCTGATATC AGTAGATTCC 1080
ATAGGGCAGA GCTGAAGCAG CTGTTCTTTG CTAATCTTGG AAGTTTATTG ATGTTTTATT 1140
TACACACCTG TACAGACAGA AGATAATAGA GATTGTTTAG AAATATTCTG TCACCTATAA 1200
TGACTAAGCA TTGCTATAAT GGAGCATGTG GTTTCCTTAA TTGAAGAATA CCTAAATAGA 1260
AGCCCATTCT TAACTGGCCT CAGTATAAAC AGCTTGTAGT GGCAGGTCAC CAGGCCTGGA 1320
TCACAGTGCC CTACCTTGTT TTTGCTTCAT AGGCAGAATG GTGGTAAGTG GTACTCTGGC 1380
CTGGGCAAGG TCTGAGCAAG GCCTGCATTG ATGGAGGGTC CAGAGTCCAG CTCTACCATC 1440
TGCACATTTT CTTTGGAGAC TTGTGCTTAG CCCAACAGCA TGAATCATTT GCTGAAGGCT 1500
CTGGAGGTGG GCATTCCATC CACAAGTCTC CCCAATAGGG AGTACCCTGT TTGGACATAC 1560
AGGGTAGTCA CACATATGGG TTTTAAATCT TGTTCTTAGG ATATTTTCAG GAAAAGCTCT 1620
GGCCCACACG TTTAGGACCA TTTCCTGGGC AGCATTGGAA GGAGTGGTAG AGGTCATGCA 1680
GGCCTGCCCT GTCTTGTGTG CAGGAAAAGA ATGAGTTGTT GGTCTACACT GAGGCCGGGA 1740
TGGGAGGCCT GCCCCTTACA GCAGCGCCGG CTGAACTCCA GGCTGGCTGG TCACATGGTG 1800
CCCAGCAGCT GACTTTTTAT CAGCTTGGCT GGATTAGAAT GAGCTGAAAG AAGAGCCATA 1860
CGCCGGTGTT CCTTGGTTAC ATGGTGCCCT GTAGTTGATA TTTATAGCAA TTAAAAAGCA 1920
TTGTCAGTGT CAGAACTTAG TAAGTGAGGT TGTGTGGATA GTGCTGGGCC TCATCAACTT 1980
ATCAGCTGTG CGAGGGCCTT TGAGCATGGG TGTGGCTCCA TGCAGCAAGG AGACCGGAGC 2040
CTGCCCCACC CGCGCCGCGG ATTATTTAGA CAAGGTGGCA GTAATGTGGT GACCAAGGGT 2100
AGCTACGTGG GTGGGCTGGG CTTGTTCTGT GGCTGAGGTG GAGTAGGGAG GGCAGCTGGA 2160
GTGGCGTCTG TAGGGGCTAT GGATAGATGA GAGGAAGTGG TCTCATCAGT CCAGAGCCAC 2220
CCGTAGTCAT AGAGCTTGGG CTAAGTTGTA ACACTCTCCT CATGTTCCTC ATCAACTTCT 2280
TGAACAAATG CAAGTATATG TGCAAGGACT TTATAATTTT TTTTTTTTTT TCGAGATGGA 2340
GTCTCGCTCT GTCTCCAGGC TGGAGTGCAG TGGCACGATC TCGGCCCACT GCAACCTCCG 2400
ACTCCCTGAT TCAAGCTATT CTCCTGCCTC AGCCTCCTGA GTAATGGGGA TTACGGGCAC 2460
GCACCACCAC GCCCAGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCATGTTGG 2520
CCAGGATGGT CTCAATCTCC TGACCTCATG ATCCGCCCGC CTCAGCCTCC CAGAATGCTG 2580
GGATTGCAGG CGTGAGCCAC TACACCTGGC CGGACTTTAT AAATTTTAAA AAGCTGCAAA 2640
TGCAGGACCA 2650