EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS007-07556 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr18:3622400-3625050 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr18:3622800-3622821TTTTTCTTTTTCTTTTTTTTT+6.09
MyogMA0500.1chr18:3623995-3624006GACAGCTGCTG+6.14
Nr2f6(var.2)MA0728.1chr18:3623022-3623037TGAACTCCTGACCTC-6.22
Tcf12MA0521.1chr18:3623995-3624006GACAGCTGCTG+6.02
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_02763chr18:3622267-3626272Astrocytes
SE_13339chr18:3621069-3626272CD34_Primary_RO01536
SE_14380chr18:3620686-3627455CD4_Memory_Primary_7pool
SE_20735chr18:3621025-3626633CD8_Memory_7pool
SE_23414chr18:3623672-3625530Colon_Crypt_1
SE_24111chr18:3622425-3622782Colon_Crypt_2
SE_24111chr18:3623695-3624667Colon_Crypt_2
SE_24111chr18:3624759-3625440Colon_Crypt_2
SE_28047chr18:3623465-3625811Fetal_Intestine
SE_29024chr18:3623576-3625604Fetal_Intestine_Large
SE_29644chr18:3623207-3625384Fetal_Muscle
SE_31815chr18:3622333-3622892Gastric
SE_31815chr18:3622925-3625600Gastric
SE_33785chr18:3622156-3626532HCC1954
SE_34235chr18:3601188-3628195HCT-116
SE_34627chr18:3620675-3627737HeLa
SE_36484chr18:3622231-3626476HMEC
SE_37649chr18:3621501-3626595HSMMtube
SE_39841chr18:3620699-3627829K562
SE_44173chr18:3621676-3626130NHDF-Ad
SE_44760chr18:3621598-3626138NHLF
SE_46537chr18:3621539-3626487Osteoblasts
SE_47120chr18:3601015-3628781Panc1
SE_50254chr18:3622276-3622943Sigmoid_Colon
SE_50254chr18:3622960-3625633Sigmoid_Colon
SE_52285chr18:3621783-3625994Skeletal_Muscle_Myoblast
SE_52452chr18:3622290-3625714Small_Intestine
SE_56746chr18:3622323-3622807VACO_400
SE_56746chr18:3623021-3626737VACO_400
SE_57446chr18:3622361-3622793VACO_503
SE_57446chr18:3623391-3624648VACO_503
SE_57446chr18:3624737-3625557VACO_503
SE_64064chr18:3621712-3626001HSMM
SE_64950chr18:3622265-3626251NHEK
SE_67704chr18:3621437-3626982u87
SE_68903chr18:3623657-3625587H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1836238723624258
chr1836243383624601
Number: 1             
IDChromosomeStartEnd
GH18I003615chr1836151063627844
Enhancer Sequence
TCCTAAGCTG ATTATTTCAT GATTCATGCT TGGCTTGGGA TCTGGGAATG ATGGGGAAAG 60
TTACTCTCTC AAAGATTGGC TCTGTCCCCT GGGGAATGTG GGAGGAGGGA GAGTCCAGAA 120
TTCGGCTTCC AAGTGGCCAC AAGTCTGGCC TCCTTCACCC AGCCTGTGCC TGTGTCCACA 180
GGACAAGATC CAGGCTGACA GCCATGCACT GCCACACCAC TGTCCCAGAC TGGGGCAAGC 240
AGAAGGGGGC TGTTTCCTCT CATCTTTCCC CAATTTCTTG CTTGCCAGAG GCAATCCTAA 300
CTTGGCTAGC GGAAAGATAA TCACTTTTGA AAACATGAGT GAGGTCAGCC CTTCCAGCCA 360
CAGCCTGGAG TTTGAAATTA CACATTCATT GATTTCTTTT TTTTTCTTTT TCTTTTTTTT 420
TGAGATAGAG TCTCTCTCTG TCGCCCAGGC TGGAGTGCAG TGGCACAATC TTGGCTCATT 480
GCAACCTCCG CCTCCCAGGT TCAAGTGATT CTTGTGCCTC AGCCTCCCCA GTAGATGGGA 540
CTACAGGCAT GTGCCACCAT GCCCTGTTAA TTTTTGTATT TTTAGTAGAG AAGGGGTTTC 600
ACCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCAAA TGATCCGCCT GCCTCTGCCT 660
CCCAAAGTGC TGGGATTACA CGCGTGAGCC ACCAGCCTGG CCTGATTTCA GTACTGGAAT 720
GGCCTCATGT CAGCTGGGTG ATCTTGTGTG CTGCCTCTCT GTGTCCCCAT GTCCTCACTG 780
GTGAAACAGG CATGCTAAAA GCATTGATTT AAGAGAGTTG TTGAGAGGAT CACATGAGAT 840
AATCAAGGAA AAAGTCTTAG ATCAGGGCCT GGAACAAAGT AAATGTTTAA TCCTATTAAT 900
GCAATTAATT GTGGTTAATG ACATGTCATA ATTAATAGCT ATGATTATTT TCACGAGCCC 960
TGACATTATC TTCCATTTCC AGGCTTCGCA TGTATAAGAG GTCCTAGACA CAAATTCACC 1020
TACACAAGGG ATTCAGTCCG TCTTAGGTTC TGCTAATGAC AACTCTTCTT GAAGTTCTTC 1080
AAGGCCGTGT GAAAAGGAAA AGCCAGCCGG GCACAGTGGC TCACGCCTGT AATCCCAGCA 1140
CTTTGGGAGG CTGAGGCGGG CGGATCACCT GAGGTCAGGA GTGCGAGACC AGCCTGGCCA 1200
ATGTGTCTCT ACTAAAAATA CAAAAATCAG CCGGGCGTGG TGGCGCATGC CTGTAATCCC 1260
AGCTACTCAG GAGCCTGAGG CAGGAGAATC GCTTGAACCT GGGAGGCGGA GCTTGCAGTG 1320
AGCCGAGGTC ACACTACTGC ACCCCAGCCT GAGAGACAGA GCAAGACTCC GTCTCAAAAA 1380
AAAAAAAAAA AAAAAAGGAA AACCCCCCTA GAAAATGCTT TTCCCGTTGC TTCCCTGCTA 1440
ATGGGCCTTT TTCATCAGGG CAGCCTCCAG CCTTAGGATG TGGCCGGTCC CCGTGCGGAT 1500
GCCCGTTTCC CCTCCTGCCT GCATTCATCT GACCGGTTCA GTGGGATCTG GTACTTTTCC 1560
TCCCTCCTCC TCGTGCTGGG CTTCCACATC ATCCAGACAG CTGCTGCCAC ATTCCACCGC 1620
TCCAGCAGCG GAAGTAAGGC ACATTTAGGC CCTTTCTGGG TGAGTGACAG CATTTGAGAT 1680
GAGATTAATC AAATGCCAGT GTTAGGGGAA AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC 1740
ACCTTTCTCA TGACACAGAG CATGAGCCTG TCCAACGGTT GGCCTGTGCG TCAACCTCTG 1800
GCCAGGAGAC AACGGGCGCC TGTGACCTGG GCGTGAACCG TCTGTTTGTG CGCATAGGTC 1860
TGACACTGCT GCTGGGCGAG CCTGCGTGCC CCTGCCCCGC GGTCCATTGA CTGTGCCGCT 1920
GAGCACAGGC AGGGATGTGT GCCTGTCGCC CTGGGCCGCT GTCCCCTGAC GGCAGATGAG 1980
ATATTCTTCC AGCTCAACAC TGATGTTGCA GGGTTTTTCC TCACCTACCG CATGACGACT 2040
GAATGAAAGC ATTCCAGGAA ACCAAAAGGG CTGGGCAGGC CTCTGGAATT TCAAAGCCGA 2100
CAGCCTGGCC CTGCTGGCAG CTCATTTCTG CCGCGTCATT TTCTCTGAAC TGTAGGAGTA 2160
GTTTTGTAGC AAACTTATCA CCAAAATCCC ACAAATGTTA AGCATTACCC TTCTTAGAAA 2220
GGAAAAGCCT ACTTACTTTT CCCCATTGGA AGACTTCAAT TTTTTAAGAT TCAAGAAATC 2280
CCCAAAAGTC ATGATAAAGA AGAGGGAAAA CAGACTGAGC ATACCCATCC CCTTTTAAAT 2340
TCAAATTTAT TTTGTTTTTT TCTGCTTAGC TACAGGGAAG GTTTGATCAT ATCACATCTG 2400
AGTTAGGCCA TATGCACCCA GGGGGAATCT CAAGAGCAAA CTAATCTAAA CTCCAAGAAA 2460
TAGACCACTA AGACCCACCC AGGTAGTACT CACTGAACGC TCTTCCTGCC TCTCATAAGA 2520
ACCAAAAATA GCGGTTTCCC GCAGATGCTC CCAGAAGCAA AGTCTACCTA CCACACACAC 2580
AATATGCAGA AGGGAAAAAC CCAAGCCACA AGTCCCTAAA CGCCTGAGTC GTGACTCATG 2640
GAGGCTGTCC 2650