EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS104-54587 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr7:44672440-44675320 
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: 2             
ChromosomeStartEnd
chr74467494144675231
chr74467284644675300
Number: 1             
IDChromosomeStartEnd
GH07I044628chr74466800844681598
Enhancer Sequence
TCTCCTGACC TCATGATCCG CCTGGTGGAT GTTTTTAATG ATTATCCTTT TGTACTGTAC 60
TTTAAGAAAA AAAAAATTTT GTTTAATGTC AGAAATTGAA AGGGGAGAGA GATCAAAAAT 120
ACCTTAATGG GGCCAGGCAC AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCTGA 180
GGTGGGCAGA TCACGAGGTC AGGAGATCGA GACCATCCTG GCTAACATGG TGAAACCCTG 240
TCTGTACTAA AAATACAAAA AATTAGCCGG GCATGGTGGC GCACCCCTGT AGTCCCAGCT 300
ACTTGGGAAG CTGAGGCAGG AGAATGGCGT GAACCTGGGA GGCGGAGCTT TTAGTGAGCC 360
AAGATTGAGC CACTGCACTC TAGCCTGGGC AACAGAGCGA GACTCTGTGT CAAAAAAAAA 420
AAAAAAAAAA AAACCCTCAA TGGGAAAGTA GACTCCAAGA GTGAAAAGGA GCAAATTGTT 480
CCAGTGAGTT CCATTCTGTA GCACAGGTGG CCACAGGTGC TTGCCTTTGA GGAAATGAAA 540
GAGCCATGCT TTGTAAGTCA GAGGCAGGCT CAGCTTCCCC GCACAGTCTG AAGCTGGGTG 600
GCGGTGAGAA ATTACTAAAA GGTTAGTGCC GGTTTTTTAG ATGAAGTCAT CATGTTATTA 660
AAAAATAGTC TGTTTAGTCT CTAGGTTACT GTTCTCTGGC TCCCCTCCCC ATCCAAGACT 720
CCCTTGGAGG GAGGTTTGAG GACTTTGGGA TTCTCATATC TCTTCGCGTC CATGATTGGA 780
TCGTGAGGTG AGGAGATAGC CTTTAGAACC CTCTCTTTGA GTGGTCAGTC ACGTGGTATT 840
CCCTCTGAAA CCCTGGAGCA GATGCTTTGT GTAGCTGGGC TGGGGTTCCC CCAAATAGGG 900
TTGCATAATT ATTGAGGACA GATGAGGCCT CAACCAGACG ACCACAGGTG ACCCCAGACT 960
GTGGGTCTTC CTCACCTCCT TGAGAGTTGC AATTCTGAGA GCTGATAAAA TGTGCCATTG 1020
TGTGCAGATC TGGGTAGTTT GAAGCGTTCT CATTTCCTGA GGTGTGTCAG AAAGACTGCG 1080
TGAGAAAGGG GTCACAGTAT CTTGGATGTC ATCTTTTCAT GCAGTAAAAA GTCTGGTTTC 1140
CATGAATGTT TGTATAACAA ACCACCTCAA AACTTGGCAC CAGTGTAGCA TGTCTCATGA 1200
CTCTGTGGGT TGGCTAGGTT TCCCCACTCC TCCCACTGCC AGCTCCCTTG GAGCTGAGGC 1260
TCACACCAGG CTAGAAGCCA TGAAGGCCTC TGATGTGTCT GGCAGTTTGT GCTGGCTGTT 1320
CACTGGGCCC TGCCATCCTC CAGTAGGCCG GAGCGATTCC TGCACAAAGT CCCAGAGTAG 1380
CTCCAGACAG GGAAAAGAAA GGCTGTGGGG CCTTTGAGGC CTAGGTCCAG ACCGTACACT 1440
GCTACTCCCC ACGCCATTAC CTTGGTTAGA GCAAGTCACA GACAACCCTT AGGGACATCC 1500
GTTTGGGGAG AGGAAAAGGC ATGGCCACTG GACAGCCCTC CACAGCTCTT TTCATAATGA 1560
CCTGATAGAG CAGCCACCTT TAGTCTAGTG CAGAATCCCA GCAAATATCA TTCTGATATC 1620
AGTAGATTCC ATAGGGCAGA GCTGAAGCAG CTGTTCTTTG CTAATCTTGG AAGTTTATTG 1680
ATGTTTTATT TACACACCTG TACAGACAGA AGATAATAGA GATTGTTTAG AAATATTCTG 1740
TCACCTATAA TGACTAAGCA TTGCTATAAT GGAGCATGTG GTTTCCTTAA TTGAAGAATA 1800
CCTAAATAGA AGCCCATTCT TAACTGGCCT CAGTATAAAC AGCTTGTAGT GGCAGGTCAC 1860
CAGGCCTGGA TCACAGTGCC CTACCTTGTT TTTGCTTCAT AGGCAGAATG GTGGTAAGTG 1920
GTACTCTGGC CTGGGCAAGG TCTGAGCAAG GCCTGCATTG ATGGAGGGTC CAGAGTCCAG 1980
CTCTACCATC TGCACATTTT CTTTGGAGAC TTGTGCTTAG CCCAACAGCA TGAATCATTT 2040
GCTGAAGGCT CTGGAGGTGG GCATTCCATC CACAAGTCTC CCCAATAGGG AGTACCCTGT 2100
TTGGACATAC AGGGTAGTCA CACATATGGG TTTTAAATCT TGTTCTTAGG ATATTTTCAG 2160
GAAAAGCTCT GGCCCACACG TTTAGGACCA TTTCCTGGGC AGCATTGGAA GGAGTGGTAG 2220
AGGTCATGCA GGCCTGCCCT GTCTTGTGTG CAGGAAAAGA ATGAGTTGTT GGTCTACACT 2280
GAGGCCGGGA TGGGAGGCCT GCCCCTTACA GCAGCGCCGG CTGAACTCCA GGCTGGCTGG 2340
TCACATGGTG CCCAGCAGCT GACTTTTTAT CAGCTTGGCT GGATTAGAAT GAGCTGAAAG 2400
AAGAGCCATA CGCCGGTGTT CCTTGGTTAC ATGGTGCCCT GTAGTTGATA TTTATAGCAA 2460
TTAAAAAGCA TTGTCAGTGT CAGAACTTAG TAAGTGAGGT TGTGTGGATA GTGCTGGGCC 2520
TCATCAACTT ATCAGCTGTG CGAGGGCCTT TGAGCATGGG TGTGGCTCCA TGCAGCAAGG 2580
AGACCGGAGC CTGCCCCACC CGCGCCGCGG ATTATTTAGA CAAGGTGGCA GTAATGTGGT 2640
GACCAAGGGT AGCTACGTGG GTGGGCTGGG CTTGTTCTGT GGCTGAGGTG GAGTAGGGAG 2700
GGCAGCTGGA GTGGCGTCTG TAGGGGCTAT GGATAGATGA GAGGAAGTGG TCTCATCAGT 2760
CCAGAGCCAC CCGTAGTCAT AGAGCTTGGG CTAAGTTGTA ACACTCTCCT CATGTTCCTC 2820
ATCAACTTCT TGAACAAATG CAAGTATATG TGCAAGGACT TTATAATTTT TTTTTTTTTT 2880