EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-21524 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr7:44673110-44675320 
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
TGTTTAGTCT CTAGGTTACT GTTCTCTGGC TCCCCTCCCC ATCCAAGACT CCCTTGGAGG 60
GAGGTTTGAG GACTTTGGGA TTCTCATATC TCTTCGCGTC CATGATTGGA TCGTGAGGTG 120
AGGAGATAGC CTTTAGAACC CTCTCTTTGA GTGGTCAGTC ACGTGGTATT CCCTCTGAAA 180
CCCTGGAGCA GATGCTTTGT GTAGCTGGGC TGGGGTTCCC CCAAATAGGG TTGCATAATT 240
ATTGAGGACA GATGAGGCCT CAACCAGACG ACCACAGGTG ACCCCAGACT GTGGGTCTTC 300
CTCACCTCCT TGAGAGTTGC AATTCTGAGA GCTGATAAAA TGTGCCATTG TGTGCAGATC 360
TGGGTAGTTT GAAGCGTTCT CATTTCCTGA GGTGTGTCAG AAAGACTGCG TGAGAAAGGG 420
GTCACAGTAT CTTGGATGTC ATCTTTTCAT GCAGTAAAAA GTCTGGTTTC CATGAATGTT 480
TGTATAACAA ACCACCTCAA AACTTGGCAC CAGTGTAGCA TGTCTCATGA CTCTGTGGGT 540
TGGCTAGGTT TCCCCACTCC TCCCACTGCC AGCTCCCTTG GAGCTGAGGC TCACACCAGG 600
CTAGAAGCCA TGAAGGCCTC TGATGTGTCT GGCAGTTTGT GCTGGCTGTT CACTGGGCCC 660
TGCCATCCTC CAGTAGGCCG GAGCGATTCC TGCACAAAGT CCCAGAGTAG CTCCAGACAG 720
GGAAAAGAAA GGCTGTGGGG CCTTTGAGGC CTAGGTCCAG ACCGTACACT GCTACTCCCC 780
ACGCCATTAC CTTGGTTAGA GCAAGTCACA GACAACCCTT AGGGACATCC GTTTGGGGAG 840
AGGAAAAGGC ATGGCCACTG GACAGCCCTC CACAGCTCTT TTCATAATGA CCTGATAGAG 900
CAGCCACCTT TAGTCTAGTG CAGAATCCCA GCAAATATCA TTCTGATATC AGTAGATTCC 960
ATAGGGCAGA GCTGAAGCAG CTGTTCTTTG CTAATCTTGG AAGTTTATTG ATGTTTTATT 1020
TACACACCTG TACAGACAGA AGATAATAGA GATTGTTTAG AAATATTCTG TCACCTATAA 1080
TGACTAAGCA TTGCTATAAT GGAGCATGTG GTTTCCTTAA TTGAAGAATA CCTAAATAGA 1140
AGCCCATTCT TAACTGGCCT CAGTATAAAC AGCTTGTAGT GGCAGGTCAC CAGGCCTGGA 1200
TCACAGTGCC CTACCTTGTT TTTGCTTCAT AGGCAGAATG GTGGTAAGTG GTACTCTGGC 1260
CTGGGCAAGG TCTGAGCAAG GCCTGCATTG ATGGAGGGTC CAGAGTCCAG CTCTACCATC 1320
TGCACATTTT CTTTGGAGAC TTGTGCTTAG CCCAACAGCA TGAATCATTT GCTGAAGGCT 1380
CTGGAGGTGG GCATTCCATC CACAAGTCTC CCCAATAGGG AGTACCCTGT TTGGACATAC 1440
AGGGTAGTCA CACATATGGG TTTTAAATCT TGTTCTTAGG ATATTTTCAG GAAAAGCTCT 1500
GGCCCACACG TTTAGGACCA TTTCCTGGGC AGCATTGGAA GGAGTGGTAG AGGTCATGCA 1560
GGCCTGCCCT GTCTTGTGTG CAGGAAAAGA ATGAGTTGTT GGTCTACACT GAGGCCGGGA 1620
TGGGAGGCCT GCCCCTTACA GCAGCGCCGG CTGAACTCCA GGCTGGCTGG TCACATGGTG 1680
CCCAGCAGCT GACTTTTTAT CAGCTTGGCT GGATTAGAAT GAGCTGAAAG AAGAGCCATA 1740
CGCCGGTGTT CCTTGGTTAC ATGGTGCCCT GTAGTTGATA TTTATAGCAA TTAAAAAGCA 1800
TTGTCAGTGT CAGAACTTAG TAAGTGAGGT TGTGTGGATA GTGCTGGGCC TCATCAACTT 1860
ATCAGCTGTG CGAGGGCCTT TGAGCATGGG TGTGGCTCCA TGCAGCAAGG AGACCGGAGC 1920
CTGCCCCACC CGCGCCGCGG ATTATTTAGA CAAGGTGGCA GTAATGTGGT GACCAAGGGT 1980
AGCTACGTGG GTGGGCTGGG CTTGTTCTGT GGCTGAGGTG GAGTAGGGAG GGCAGCTGGA 2040
GTGGCGTCTG TAGGGGCTAT GGATAGATGA GAGGAAGTGG TCTCATCAGT CCAGAGCCAC 2100
CCGTAGTCAT AGAGCTTGGG CTAAGTTGTA ACACTCTCCT CATGTTCCTC ATCAACTTCT 2160
TGAACAAATG CAAGTATATG TGCAAGGACT TTATAATTTT TTTTTTTTTT 2210