EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-13697 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:11205150-11207750 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
chr191120634811207740
Enhancer Sequence
TTTGTTCGTT TGTTTTTATT TTTTGAGACA GAGTCTCCCG CCCAGGCTGG AGCGCAGATC 60
ACTGCATCCT TGACCTCCCA GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG 120
GGATTACAGG TGTGTGCCAC TATGCTTGGC TAAGTTGTGT ATTTTTTGTA GAGATGGGGT 180
TCAAGGGATT CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT 240
CCCTCCTCAG CCTCCCAAGG TGCTGGGGAA ATCCACTTTT GAAACATTGT CTGGAGAGTT 300
GCCCAGGTGG TAGATCACAG AAATAGGTCA TCGTGGGGTC CTTCCCATGG GTGCAGTCTT 360
GAGCCACCTG TGGCCAGCAA ATATTTGGAG AATAATAGTC AGGGGAGAGC TTGAGGTCCA 420
GGGAAAGGTT TTGTTTTTCT TCAGGGAAAG GTTTTTATTG TTCTTTATCC CTCCTTAAAG 480
GACCTTCAGG TGTTACTGAC ATTCCCGGTC TACCCAGTGG CACATTTAGT TTGTAAGCTG 540
GGCCCTCGTA CAGAGGTAGG GAGGTGAGAG CATTGGATTA GTGGTCACCA AAGCTGCGGT 600
CACCTAGTGG GGTGATCAGA GGCTCCTCCC TTAAGATCTT GATTGCCAAC GCCTCTGGCC 660
CAACTTTCCT TTTTATTTAT CGCAAGCCTC CTGGAATCTC AATTGCTTTT TGCCCACCCG 720
GTGTGTCAGC ACAAGAAATG AGTCATTTCC TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG 780
AGTCAGTGAG GTGTGTACGA TATTGTCAAA GCGGGGTGTG TACAGTATTG ACAGATCTGT 840
AGTTGGGCAA GAGAATTATC AGAGTTTGTG ACCACAGCAG ATTCCAAAGC TCGACTCATT 900
TTCTTCTCTC TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG 960
CTCTGTTGCC CAGGCTGGAG TGCAGTGGCA CAATCTGGGC TCACTGCAGC CCCTGCCTCC 1020
TGGGTTCAAA TGATTCTCAT GTTTCAGCCT CCCGAGTAGC TGCAATTACA GGCATTCGGG 1080
TTCAAGTGAT TCTCCTGCCT CAGCCACCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA 1140
CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG 1200
TCTCGAACTC CTGAACTCAG GTGATCCGCC CACTTCGGCC TCCCAAAGTG CTGAGATTAC 1260
AGACGTGAGT CACCGCGCCC AGCCTGTTCT GTTCTTTAAT TCTCAAAACA CCCTCTAGGA 1320
AGTAGAGACT GCCATTCTCC CCCATTTTAC AGATCAGGAA ACTGAGTCCC AGAAGGATTT 1380
AGTCAGTTAC CCAAGTTGTT CTAGTTAAAT GGCCTGGAAA GCCAGTGAAG CCCAGGATTG 1440
TCTATCTAAC CCCCTTACTA CTCTAACTTT CAGGGAATCC ACATGAATGT GCTGGGTCAA 1500
CCATCAAAGT TGAAATGGAT AAAGGGGGCT GGATGCGGTG GCTGATGCCT GTAATCCTAG 1560
CACTTTGGGA GGCCGAGATG GGTGGGTGGA TTGCTTGAGC CCAAGAGTTT GAGACCAGCC 1620
TGGGCAACAT AGTGAGACAC CTGTCTCTGC AAAAAATAAA TAAAAAGTTA GCTGAGTGTG 1680
ATGGTGCACC CCTCTAGTCA CAGCTGTTGA GTTAGGCTTA GGCAGGAGGA TCGCATGAAC 1740
CTGGGAGGTG GAGGCGGCCG TGAGCCTCAG TCATGCCACT GCACTCCAAC CTGGGCAACA 1800
GAGTGAAAGC CGGTGTCCGA AAGAGAAAGA AAAAAAGACA TAGATACATC TTTTAAAGTT 1860
AGGTTGTATG TTAATTACCT ACAACTCAGT TTCAACTGTG CTTAAAGGAG GAAATGACTC 1920
ATTTCTTGCT ACATATCAAA TTAGCCCAAA ATGTAGTGGC TTAAAACAAC ACATTTATGA 1980
TTTCTCAGTT TTTGCGTGTC AGGAATTTGG AAGCAGCACA GCTAGACGGT TCCAGCTCAG 2040
GGTCTCTCAT GAAGTTGCAA TCAAAATATT GGCAGGAGAG AAAAACATAT TTTCAGAAGC 2100
TGCAGGCATA GGAAGACTTG GCTGGGGTTG AAGGATCCAC TTCCAAGATG GCGCACTCAG 2160
TGGCTCTTGG CTGGAGGCCT CAGTTCCCTG CTGCGTGGAG CTCTCCCTCC AGCTGCTTGA 2220
GTGGACTCAT GACATGCAGC TGGCCTCCCC TGGAGCAGTC GATCCAACAA TGAGCATGGC 2280
CATGAACTAG GCTCAGAAGC CACTCCCTGT CGTCTCTACA TTTTCCTATC AGAAGCAAGT 2340
CATTAAAAGT CCAGTGCCAC TCCAGGGGAG ACGAATTAGG CTCTGCCTTC TGAAAGGATT 2400
ATCACAGAAG ATGCGGTCCT ATATTCTTTT TTTAAAATTA TTCTTTTTTT TATTTTGTAG 2460
AGATGGGGTC TTGGTATGTT GCCTAGGCCA GTCTGGAATT CCTGGGCTCA AACAATCCTG 2520
TCTCTGCCTC CCAAAGTGTT GGGATTACAG GCATGAGCCA CTGCACCTGG TCATGTGGTC 2580
ATATTTTCTT TTTCTTTTTT 2600