EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-51898 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr7:44677420-44680510 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr5a2MA0505.1chr7:44679698-44679713GCTGACCTTGACCCT-6.88
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_09293chr7:44668114-44680616CD14
SE_12002chr7:44675737-44680602CD3
SE_14587chr7:44668357-44680825CD4_Memory_Primary_7pool
SE_15490chr7:44676270-44680378CD4_Memory_Primary_8pool
SE_16434chr7:44672525-44680593CD4_Naive_Primary_8pool
SE_16951chr7:44675465-44680529CD4p_CD225int_CD127p_Tmem
SE_17851chr7:44668129-44680829CD4p_CD25-_CD45ROp_Memory
SE_18656chr7:44670100-44680815CD4p_CD25-_Il17-_PMAstim_Th
SE_19294chr7:44675433-44680659CD4p_CD25-_Il17p_PMAstim_Th17
SE_20655chr7:44668188-44680617CD56
SE_21218chr7:44672481-44680578CD8_Memory_7pool
SE_22840chr7:44672479-44680608CD8_primiary
SE_24636chr7:44677413-44677804Colon_Crypt_2
SE_24636chr7:44677846-44680063Colon_Crypt_2
SE_26120chr7:44672338-44680827Duodenum_Smooth_Muscle
SE_27427chr7:44675393-44680685Esophagus
SE_27654chr7:44668239-44680825Fetal_Intestine
SE_28557chr7:44668586-44680821Fetal_Intestine_Large
SE_32407chr7:44672719-44680093Gastric
SE_32407chr7:44680106-44680586Gastric
SE_34691chr7:44670606-44681894HeLa
SE_36719chr7:44676722-44680551HMEC
SE_37328chr7:44672508-44680850HSMMtube
SE_40682chr7:44672552-44680631Left_Ventricle
SE_42075chr7:44679237-44679954LNCaP
SE_42544chr7:44672671-44680682Lung
SE_43768chr7:44675436-44680621MM1S
SE_46384chr7:44676438-44680713Osteoblasts
SE_48519chr7:44672671-44680588Psoas_Muscle
SE_49693chr7:44677432-44677748Right_Ventricle
SE_49693chr7:44677999-44679961Right_Ventricle
SE_50531chr7:44677170-44680609Sigmoid_Colon
SE_52560chr7:44672691-44680563Small_Intestine
SE_53907chr7:44672618-44680662Spleen
SE_62947chr7:44653723-44680812Tonsil
SE_64825chr7:44676532-44680626NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr74467742544680014
chr74467939244679514
chr74468010144680272
chr74467762844678244
chr74467862244679047
Number: 1             
IDChromosomeStartEnd
GH07I044628chr74466800844681598
Enhancer Sequence
AAAAAAAAAA AATGGTATTC ATTTTTTGAC ATGGTACATC CTGCACACAT CTGACACTCT 60
TAGGAAAATG TTTATGTGTG GTAAGAACTT CATCAGAATC CCATAGCCCC TTGCAGGGCT 120
CAGAAGTTGG CCTTTTGGGA GTGAGTGCTT TCCCGCACCC CTCCCCTGGC CCAGGACCCC 180
TCACTCCTTC TGGCAGCTTC CTGCCCCTTG AATGTCATTT ACAACCTTGC CCACTTACCT 240
TAACATTTTA ACCTTTTCCC CCTTATCAGT GACATTGTCA TTGGTGGTCA GAGAATTAAC 300
TGTGTGTAAC TGTATATTTG AGGCAAGGCA AGGGGACAGA TATTTTCCTT ACGTTATTAG 360
TTGTGCAACA GAAGCCAATT AAGAGATTGG AGAGATGAAT AACACTAGTG ATGGGTTGCA 420
ACTTGGGTGT GGAGCTGGGC ACACCCACGT ACGTCATTGT GACTCAGAAG TCCCTGTCAC 480
CGCCCTGAGC CAAGTACTAA AGTAAGGCCC AAATACCACA CTTACTTCAT AAAGAAACCA 540
AAGTCTGACT GCCTCCATTT CTCATGAGTG AAAAACTGTT TCTATTATAG GAAACTTAGG 600
TCTTCAGTGT GTTTGATGGT AGCATGCTAT TAGATTGTGT ATTCTCAAGT CTGATTTTCC 660
CCATTACTGT GCTTTCTCCT TTTCACTTCT GCTTTGTCAC TTGGAATGTT TCTAGAAGTA 720
GAAGTCACTG CCCCTGCCTA CATCAGACTG CAATTCCGGG ACATCCAGGC AACAGCAAGG 780
GATAATTAGG AATAAATTTG GCTGGAAGAA AGGGAAAATG CAGCTTAGGC AGCCTAAACC 840
AACAGGCTTA TTTTTCTCAC TCAGTAAGAG AGCTGAGGTC GCCTGACTCA GCTCAGGTTC 900
TCAGTGAGCC ATCAGCCACC AGGTGCCACC TTTCAGTGAG TGGGCTTCTA TCCCTTCCAG 960
GTGTCTCTTC ATGCTCCATG GGAATTAGAT GGGACATGCT TTGACTCTCT CTTCCAGAAG 1020
CTTTCTCTTC TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT 1080
CTTGATTTAT CCCCCAGGAT GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG 1140
TGTACAGTAA GGGCTGGGAG TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT 1200
AAGCGACCAT GTGAAGGGAG AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC 1260
TGCGGGAAGG AAGGAGCATG ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC 1320
AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG 1380
AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG 1440
GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA 1500
TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG 1560
GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC 1620
TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC 1680
TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT 1740
AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA 1800
TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT 1860
TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA 1920
AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG 1980
GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC 2040
TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC 2100
TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG 2160
AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC 2220
TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC 2280
TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA 2340
TTGTTGAGCC CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT 2400
GTTACTAGAG TGACCAGAGT TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT 2460
AATACCCTGC CTGGTGACTG CTGTGTGTAA ATTCTGCCTG AGCCCACATC TCTCCAGTGG 2520
GAATATGATT GACATTCCAG GTGCTCTAAG TAAGTTGGAA AAGCCCACAG AGAGCCTCAG 2580
TAAAAGTTAG CTATACCTAT CCCTGCTGCT ATTGGTGGGT TTTTTTTGTT TTGTTTTGTT 2640
TTACTATTTT AATTGTTATT CAAAGCTAAT TTTATTGAAA AGAAGTAAAC TTGTGATTTT 2700
GCTATGACTT TTGGCTCTGG ATCCAAAAGT GAATATTGTC CCCTAGGATA AAGGAGGCTG 2760
TCTGTACAGC TGGAGAGACT CTTGATCTAA GGTCTTGCTC TTGGGTGACT TTGCCCTGTG 2820
TTTCTGGACA CTTAATGGGT TTTACGAAAT AGAAGAAAAT GTTTTAGGGG TTTAATAAAG 2880
TTTGGGTTGT GCTGTTCTCC AGTACTTACT GGGTTTGAGG GTCATGCCCT ATCCATGAAC 2940
CTGTTGTGGC CCCAGGGAAC TAAGTAAGTG TCTACAGCTA GACTTGGGGT GCGGGTCACA 3000
TGGTGTGAGG GTAGACATTC TAGCACTGGA GCAAGTTTGG GGTAAAGAAA AATTTTGATT 3060
AGGTTTTTTG TGGGTTTTTT TTTTTTTCTT 3090